Note: ∅ = Latent Construct.
ITI ∅ = IT Integration; TRST ∅ = Trust; IS ∅ = Information Sharing; CG ∅ = Contractual Governance; ICT ∅ = Information & Communication Technology; INNOV ∅ = Innovativeness; AGLTY ∅ = Agility; VCC ∅ = Value Chain Competitiveness.
i = indicator variable 1; j = indicator variable 2; k = indicator variable 3.
l = indicator variable 4; m = indicator variable 5; n = indicator variable 6.
The next step is to determine the discriminating validity of the constructs, once the reliability of the reflective constructs had been established. Discriminant validity demonstrates whether the constructs in the model are highly correlated among them or not. Heterotrait-Monotrait Ratio (HTMT) was used to evaluate discriminant validity as recommended by Henseler and his research fellows [ 114 ]. The results in Table 2 demonstrate that HTMT values are significantly lower than the conservative threshold (HTMT 0.85 ), meaning that all variables in the conceptual model have discriminant validity.
CG | ITI | ICT | IS | INNOV | TRST | AGLTY | |
---|---|---|---|---|---|---|---|
0.563 | |||||||
0.313 | 0.295 | ||||||
0.449 | 0.431 | 0.288 | |||||
0.595 | 0.547 | 0.534 | 0.522 | ||||
0.536 | 0.510 | 0.342 | 0.453 | 0.551 | |||
0.641 | 0.615 | 0.477 | 0.531 | 0.658 | 0.605 | ||
0.607 | 0.454 | 0.364 | 0.456 | 0.579 | 0.532 | 0.643 |
Note: ITI ∅ = IT Integration; TRST ∅ = Trust; IS ∅ = Information Sharing; CG ∅ = Contractual Governance; ICT ∅ = Information & Communication Technology; INNOV ∅ = Innovativeness; AGLTY ∅ = Agility; VCC ∅ = Value Chain Competitiveness.
Thus, the proposed theoretical model was deemed appropriate, with verification of sufficient reliability, convergent validity, and discriminating validity.
According to J. Hair et al [ 115 ] PLS-structural equation modelling is always the preferred SEM method when the research objective is to prediction of relationships between the constructs. The evaluation of the inner (structural) model included observing the predictive relevancy of the proposed model and the relationships between the constructs. The major criteria for assessing the inner structural model are the coefficient of determination (R 2 ), path coefficient (β value), and T-statistic value. The other valuable methods used for measuring structural model included the predictive relevance of the model (Q 2 ), effect size (ƒ 2 ), and goodness-of-fit (GOF) index.
In the regression analysis, the path coefficients and the standardized β coefficient were similar. The significance level of the hypothesis was checked using the β value. β is defined as the anticipated variance in the endogenous constructs for a unit variation in the exogenous construct(s). The greater the β-value, the higher the significant impact on the endogenous latent structure [ 110 ] ( Table 3 ).
Hypothesized Path | Standardized Beta | t-value |
---|---|---|
Innovativeness ⇒ Value Chain Competitiveness | 0.294 | 6.099 |
Agility ⇒ Value Chain Competitiveness | 0.413 | 6.965 |
IT Integration ⇒ Innovativeness | 0.169 | 3.708 |
IT Integration ⇒ Agility | 0.228 | 5.025 |
Trust ⇒ Innovativeness | 0.156 | 3.284 |
Trust ⇒ Agility | 0.197 | 3.965 |
Information Sharing ⇒ Innovativeness | 0.184 | 3.504 |
Information Sharing ⇒ Agility | 0.156 | 3.724 |
Contractual Governance ⇒ Innovativeness | 0.236 | 5.494 |
Contractural Governance ⇒ Agility | 0.250 | 5.299 |
Information & Communication Technology ⇒ Innovativeness | 0.293 | 6.089 |
Information & Communication Technology ⇒ Agility | 0.201 | 4.538 |
“* significant for p≤0.05.”
“** significant for p≤0.01.”
“*** significant for p≤0.000.”
The path coefficients of the structural model were used to test the proposed hypotheses. All twelve structural path coefficients demonstrated at least a p-value less than 0.05. The findings of the present study indicate that all the proposed hypotheses are verified and accepted. More precisely, ITI has a significant and positive effect on INNOV ( β = 0.169, T = 3.708, p < 0.000) and AGLTY ( β = 0.228, T = 5.025, p < 0.000). Therefore, H 1 a and H 1 b are supported. Trust positively influences INNOV ( β = 0.156, T = 3.284, p < 0.000) and AGLTY ( β = 0.197, T = 3.965, p < 0.000), lending support to H 2 a and H 2 b . H 3 a and H 3 b , which proposes that IS directly affects INNOV ( β = 0.184, T = 3.504, p < 0.000) and AGLTY ( β = 0.156, T = 3.724, p < 0.000) are also accepted. As expected, CG has a significant impact on INNOV ( β = 0.236, T = 5.494, p < 0.000) and AGLTY ( β = 0.250, T = 5.999, p < 0.000), thus supporting H 4 a and H 4 b . As expected, ITC has a positive impact on INNOV ( β = 0.293, T = 6.089, p < 0.000) and AGLTY ( β = 0.201, T = 4.538, p < 0.000), thus supporting H 5 a and H 5 b . Our results also support previous research in relation to INNOV ( β = 0.294, T = 6.099, p < 0.000) and AGLTY ( β = 0.413, T = 6.0965, p < 0.000) have a positive effect on competitiveness, thereby supporting H 6 a and H 6 b . The findings in Table 3 , and ( Fig 5 ), demonstrate that value chain competitiveness could be acquired from agility and innovative financial product development.
The coefficient of determination (R 2 ) values were determined for all endogenous constructs to test the quantity of variance described in the dependent variables seen as the structural model's predictive power. According to Hair et al. [ 39 ], the R 2 value of 0.75 is substantial, 0.50 is moderate, and 0.25 is weak. As shown in Table 4 , all the independent variables (ITI, TRST, IS, CG, ICT) demonstrated a high variance, that is, 54.7% within INNOV ( R 2 : INNOV = 0.547). These five independent latent constructs explain the variance of 55.9% within agility (R2 VCA = 0.559). Whilst, INNOV and agility explained the moderate variance i.e. 40.7% in the value chain competitiveness (R 2 : VCC = 0.407).
Endogenous Construct | Relationship | Effect size | |||
---|---|---|---|---|---|
Value Chain Competitiveness | 0.407 | 0.307 | INNOV ⇒ VCC | 0.089 | Weak |
AGLTY ⇒ VCC | 0.176 | Moderate | |||
Innovativeness | 0.547 | 0.475 | ITI ⇒ INNOV | 0.039 | Weak |
TRST ⇒ INNOV | 0.034 | Weak | |||
IS ⇒ INNOV | 0.055 | Weak | |||
CG ⇒ INNOV | 0.075 | Weak | |||
ICT ⇒ INNOV | 0.162 | Moderate | |||
Agility | 0.559 | 0.393 | ITI ⇒ AGLTY | 0.074 | Weak |
TRST ⇒ AGLTY | 0.056 | Weak | |||
IS ⇒ AGLTY | 0.041 | Weak | |||
CG ⇒ AGLTY | 0.086 | Weak | |||
ICT ⇒ INNOV | 0.078 | Weak |
R 2 = Coefficient of Determination.
Q 2 = Predictive relevance of Model.
f 2 = effect size.
Predictive relevance of Model (Q 2 ) was then assessed using blindfolding procedures [ 116 ], whereas cross-validated redundancy was performed as suggested by Chin [ 110 ]. In the SEM, for a specific endogenous latent construct, the Q 2 values measured should be greater than zero. From Table 4 , it can be seen that the Q 2 values for value chain competitiveness, INNOV and AGLTY were 0.307, 0.457, and 0.393, respectively, which are statistically acceptable for predictive relevance. To check the impact of each latent exogenous construct on the latent endogenous constructs, the effect size (f 2 ) was assessed ( Table 4 ). According to Hair et al. [ 117 ] the values of effect size (f 2 ) 0.02 demonstrate a weak effect, 0.15 is a moderate effect, and 0.35 is a substantial effect. According to these guidelines, Table 5 demonstrates that ITI, TRST, IS, and CG have a weak effect on both INNOV and AGLTY, whereas ICT has a moderate effect on INNOV. Innovativeness exhibits a weak effect on value chain competitiveness, while AGLTY has a moderate effect on value chain competitiveness. In conclusion, the R 2 , Q 2 , and f 2 test results suggest that the findings drawn from this study are relatively robust.
Construct | AVE | |
---|---|---|
IT Integraton | 0.852 | |
TRUST | 0.852 | |
Information Sharing | 0.791 | |
Contractual Governance | 0.849 | |
Information and Communication Technology | 0.822 | |
INNOVATIVENESS | 0.881 | 0.547 |
AGILITY | 0.714 | 0.559 |
Value Chain Competitiveness | 0.769 | 0.407 |
0.5043 | ||
X | ||
Note: ∅ = Latent Construc.
AVE = Average Variance Extracted, R 2 = Coefficient of Determination, GoF = Goodness of Fit Index .
Partial least square structural equation modeling does not focus on the fit model. Nonetheless, Tenenhaus et al. [ 116 ] proposed the GoF as a means to validate a PLS path model globally. A good fit model demonstrates that a model is parsimonious and plausible [ 118 ]. It is calculated using the average communality (AVE values) and the average R 2 value(s). On the basis of formula, proposed by Tenenhaus et al. [ 116 ] the value of GOF = 0.642 demonstrate that the fit index is sufficiently good to support the validity of the global model. ( Table 5 ). By using Eq ( 1 ), the model’s goodness of fit is calculated as follows [ 116 ]:
SRMR is a measure of the mean absolute value of the correlation residuals. When values of SRMR = <0.08, the research model has a good fit [ 119 ] however, a lower SRMR is considered to be a better fit. Table 6 , demonstrates that the conceptual model’s SRMR was 0.045, which showed that the conceptual model had a good fit.
Estimated Model | |
---|---|
SRMR | |
d_ULS | 1.610 |
d_G | 0.631 |
Chi-Square | 1200.916 |
NFI | 0.913 |
Note: SRMR = Standardized root mean square redidual, d ULS = squared Euclidean distance d .
d _ G = geodesic distance, NFI = Normed fit Index.
In accordance with the complete evaluation of both inner (structural) model and outer (measurement) model, it was determined that all of the hypotheses were statistically significant and hence were all verified.
The contribution of organic food value chains is graphically presented in ( Fig 6 ). The illustration shows how the propose indicators enhance the competitiveness of organic food value chain by developing innovative financial product to make agile value chain finance. Through IT integration of partners, trust-based relations, governance arrangements, ITC-based knowledge, and accurate information sharing among the value chain partners that would encourage the financial institutes for the development of innovative financial products to accelerate the financial flow and to achieve competitiveness.
In this study, a number of theoretical contributions were made. The key contribution of this study was to develop a conceptual model to address the financial needs of smallholders and mitigate the financial risk by organizing value chain actors through information technology and governance arrangements. The present study applied an advanced multivariate analysis technique of the PLS path model to examine and validate the conceptual model. PLS-SEM is a very advanced technique for developing and evaluating a complex model and social science researchers must incorporate the latest techniques to manage their current and future studies. Moreover, this study fills a gap in the literature on organic farming by investigating the impact of ITI, TRST, CG, IS and ICT on value chain competitiveness through the mediating effects of INNOV and AGLTY. In this study, we explore ITI, TRST, CG, IS, and ICT can facilitate AGLTY and INNOV, and thus have a substantially positive effect on value chain competitiveness.
The study demonstrates that ITI among value chain members significantly associated to innovative product development and value chain finance agility. IT integration between value chain actors increase smooth flow of information, thereby strengthening the trustworthiness. IT based integration of value chain actors can better informed about the product prices and will give easy access to the market. The financial institutes can utilize this network to reduce the information asymmetry, and overcome the problem of financial risk. Apart from this, financial institute design innovative product that best fit for smallholders and value chain actors. Our results suggest that IT integration rapidly adopt the changes through a dynamic network of linkages of value chain actors to respond financial needs. Thus, integration of value chain actors through information technology not only increase the creditworthiness of smallholder but also enhance financial flow and improve competitiveness of organic food value chain. In line with our study Chen et al. [ 30 ] and Chia Tan et al. [ 120 ] found that IT integration between value chain actors provide the potential to continually innovate the products to catalyze finance and investment. The results from our research indicate that trust significantly influences INNOV and value chain finance agility. The better trust among value chain members in terms of close relationships, being honest and trustworthy, etc., will reduce the uncertainty and risk for creditors. The findings of the study are based on the argument of Miller and Jones [ 25 ] who claimed that trust between the producer and the buyer can drive innovation in value chain finance and continue to mitigate risks for lending institutes. IS generates frequent communication between producers and buyers. Frequent communication with farmers has a positive impact on the VCF for both producers and buyers. Prior studies found that information sharing reconcile information asymmetry issues between farmers and lending institutes [ 62 ] which leads to craft of innovative products and value chain finance agility [ 69 ]. IS provides an opportunity for financial service providers by making decisions based on right information. Thus, IS helped financial institutes to make quick decisions about changes in the market by having frequent communications with value chain actors. CG is an efficient instrument for connecting low-income growers into value chains and increasing the income of small-scale producers, thus reducing transaction costs. In this study, CG has a significant and positive impact on INNOV and value chain finance agility. Thus, acting as communication tools for transmission of information from one actor to another actor to reduce uncertainty and risks. This will strengthen the codependent relationships, and maintain relationships between smallholder, value chain partners and financial institutes. In accordance with our findings, Enquist et. al [ 75 ] found that contractual governance develops innovative products and increase inter-organizational performance. Governance arrangements were also found to have direct effects on agility that means to respond quickly [ 76 ] according to customer needs. ICT has also been positively related to agility and INNOV. The results of our study suggested that most of the respondents were well versed with information technology, particularly internet and mobile phones. Increased levels of digitalization, such as mobile services, play an important role with respect to the development of the VCF efficiency and cost-effectiveness. This fact about the positive role of ICT was also revealed by Altenbuchner et al. [ 19 ] and Aldosari et al. [ 79 ] in which they proved that the use of ICT has the ability to save from the exploitation from the middlemen who claimed a relatively high interest rate. The findings of the present study are also in accordance with Ali and Kumar [ 80 ], Oladele [ 99 ] and, Salampasis and Theodoridis [ 121 ] in which they proved that through the effective use of ICT the value chain members strengthen partnerships, reduces transaction costs, and financial risks in value chain finance. Furthermore, the results of our research revealed that AGLTY and INNOV significantly affect value chain competitiveness. Higher the INNOV in the form of trying new ideas and ways for financial product development, better the competitiveness of the organic food value chain. The findings of the present study support the results of Ngenoh et al. [ 90 ] and Dubey et al. [ 122 ] that have explored usefulness of agility and innovativeness in responding quickly to the financial needs of value chain actors, in the rapidly changing environment and gaining higher competitiveness.
This study set up a conceptual model in the organic food value chain to examine the mediating role of AGLTY and INNOV, including aspects such as ITI, TRST, CG, ICT, and IS, which can accelerate financial flow and enhance value chain competitiveness. The present study sheds light on financial constraints faced by small-scale organic wheat farmers in developing countries such as Pakistan. As such, we conclude that over many years’ financial constraints and the exploitative role of middlemen would be overcome through the ITI, trust relations, CG, ITC-based knowledge, and IS among the value chain partners that would encourage the development of innovative financial products to accelerate the financial flow and to achieve competitiveness. To address these barriers, changes at the farm and market level as well as among financial service providers and farmers might be required, which would only be possible through trust-based relations and governance arrangements. However, farmers’ trustworthy relations with value chain partners, are needed to positively harness innovative product development for swifter value chain finance. In the last, but not least, this theoretical model should not be viewed as a quick fix but as a process of test and learning.
S1 appendix, acknowledgments.
The authors would like to acknowledge to all the services and technical support provided by College of Economics and Management during research work. The authors also thank the anonymous reviewers and Prof. Dr Dejan Dragan (Academic Editor of PLOS ONE) for insightful comments and suggestions, which led to many improvements contained in this paper. The authors are deeply grateful to the editors and the anonymous reviewers for their helpful comments, which improved the quality of the paper greatly.
This work was supported by Chinese Scholarship Council and Northeast Forestry University, Harbin, Heilongjiang, China. The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Please note you do not have access to teaching notes, progress in partial least squares structural equation modeling use in logistics and supply chain management in the last decade: a structured literature review.
International Journal of Physical Distribution & Logistics Management
ISSN : 0960-0035
Article publication date: 26 September 2023
This study aims to evaluate the usage of partial least squares structural equation modeling (PLS-SEM) in journals related to logistics and supply chain management (LSCM).
Based on a structured literature review approach, the authors reviewed 401 articles in the field of LSCM applying PLS-SEM published in 15 major journals between 2014 and 2022. The analysis focused on reasons for using PLS-SEM, measurement model and structural model evaluation criteria, advanced analysis techniques and reporting practices.
LSCM researchers sometimes did not clarify the reasons for using PLS-SEM, such as sample size, complex models and non-normal distributions. Additionally, most articles exhibit limited use of measurement models and structural model evaluation techniques, leading to inappropriate use of assessment criteria. Furthermore, progress in the practical implementation of advanced analysis techniques is slow, and there is a need for improved transparency in reporting analysis algorithms.
This study contributes to the field of LSCM by providing clear criteria and steps for using PLS-SEM, enriching the understanding and advancement of research methodologies in this field.
Wang, S. , Cheah, J.-H. , Wong, C.Y. and Ramayah, T. (2023), "Progress in partial least squares structural equation modeling use in logistics and supply chain management in the last decade: a structured literature review", International Journal of Physical Distribution & Logistics Management , Vol. ahead-of-print No. ahead-of-print. https://doi.org/10.1108/IJPDLM-06-2023-0200
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Schizophrenia volume 10 , Article number: 59 ( 2024 ) Cite this article
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Depressive symptoms in Schizophrenia Spectrum Disorders (SSDs) negatively impact suicidality, prognosis, and quality of life. Despite this, efficacious treatments are limited, largely because the neural mechanisms underlying depressive symptoms in SSDs remain poorly understood. We conducted a systematic review to provide an overview of studies that investigated the neural correlates of depressive symptoms in SSDs using neuroimaging techniques. We searched MEDLINE, PsycINFO, EMBASE, Web of Science, and Cochrane Library databases from inception through June 19, 2023. Specifically, we focused on structural and functional magnetic resonance imaging (MRI), encompassing: (1) T1-weighted imaging measuring brain morphology; (2) diffusion-weighted imaging assessing white matter integrity; or (3) T2*-weighted imaging measures of brain function. Our search yielded 33 articles; 14 structural MRI studies, 18 functional (f)MRI studies, and 1 multimodal fMRI/MRI study. Reviewed studies indicate potential commonalities in the neurobiology of depressive symptoms between SSDs and major depressive disorders, particularly in subcortical and frontal brain regions, though confidence in this interpretation is limited. The review underscores a notable knowledge gap in our understanding of the neurobiology of depression in SSDs, marked by inconsistent approaches and few studies examining imaging metrics of depressive symptoms. Inconsistencies across studies’ findings emphasize the necessity for more direct and comprehensive research focusing on the neurobiology of depression in SSDs. Future studies should go beyond “total score” depression metrics and adopt more nuanced assessment approaches considering distinct subdomains. This could reveal unique neurobiological profiles and inform investigations of targeted treatments for depression in SSDs.
Depressive symptoms are highly prevalent in individuals with schizophrenia spectrum disorders (SSDs) 1 , with as many as 80% of patients experiencing a depressive episode at some point during their course of illness 2 , 3 . Depression and depressive symptoms in SSDs are associated with poorer outcomes 4 , including reduced quality of life 5 , 6 , increased burden of disease 1 , and a higher frequency of both self-harm 7 , 8 and suicide 9 , 10 . Yet, our understanding and diagnosis of depression and depressive symptoms in individuals with SSDs are limited, with therapeutic options providing little efficacy 11 , 12 , 13 .
Diagnosing and treating depression in SSDs has posed a challenge 14 . This complexity entails not only identifying general depressive symptoms but also distinguishing them from comorbid depressive disorders 15 as well as core symptom dimensions of schizophrenia, namely negative symptoms 16 , 17 , 18 . While antidepressant medications, the mainstay approach for treating major depressive disorders (MDD), are often prescribed for depression in SSDs 19 , findings from recent reviews revealed minimal to modest clinical improvements 11 , 12 . Importantly, findings from the Recovery After an Initial Schizophrenia Episode (RAISE) trial, an early treatment program for first-episode psychosis, suggested that less frequent antidepressant use may be linked to fewer side effects 13 .
Neuroimaging methods could enhance our comprehension of the pathophysiological mechanisms linked to depression in SSDs 20 . For instance, in MDD, identifying neuroimaging correlates of antidepressant treatment responses has enabled researchers to gain insights into how antidepressants impact select brain regions, perhaps leading to improved symptom outcomes 21 . Moreover, neuroimaging can serve as a tool to guide nonpharmacological interventions, such as repetitive transcranial magnetic stimulation (rTMS), allowing for more precise and individualized targeting of symptom-related circuits that optimize treatment response 22 , 23 , 24 , 25 . In light of robust evidence that rTMS mitigate depressive symptoms in MDD 26 and preliminary support in SSDs 27 , further investigation into neuroimaging correlates may inform the selection of neurostimulation targets. While our knowledge regarding the neural mechanisms underlying depression in SSDs is limited 28 , gaining a deeper understanding has the potential to enhance opportunities for effective intervention 4 .
To our knowledge, there has not been a comprehensive synthesis of existing literature on the neurobiological underpinnings of depressive symptoms in SSDs. Therefore, we conducted a systematic review to provide an overview of studies that investigate the neural correlates of depressive symptoms in SSDs using neuroimaging techniques. Specifically, we focused on structural and functional magnetic resonance imaging (MRI), encompassing T1-weighted imaging studies evaluating brain morphology (e.g., volume or thickness), diffusion MRI (dMRI) studies examining white matter metrics (e.g., fractional anisotropy (FA) or mean diffusivity (MD)), and T2*-weighted imaging studies assessing brain function (e.g., activity or connectivity).
This systematic review was conducted per the guidelines outlined in the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) 29 and registered on the International Prospective Register of Systematic Reviews (PROSPERO: CRD42023433464 ). Before registration and screening, a librarian from the Center for Addiction and Mental Health (CAMH) in Toronto, Canada reviewed the search strategy and protocol.
A systematic review of the literature was conducted using MEDLINE (Ovid), PsycINFO (Ovid), EMBASE (Ovid), Web of Science, and Cochrane Library electronic databases from inception through June 19, 2023. Figure 1 outlines the detailed search strategy used for MEDLINE; additional strategies tailored to other databases can be found in the Supplemental Materials. In summary, our search strategy encompassed Medical Subject Headings (MeSH) and keywords related to three main search blocks: SSDs, neuroimaging (structural and functional MRI, methodology of interest), and depressive symptoms (primary outcome measure). Additionally, we conducted backward and forward citation searches for all eligible studies that met the inclusion criteria.
Medical Subject Headings (MeSH) and key terms adapted for MEDLINE (Ovid). Ab indicates abstract; hw, subject heading word; kf, keyword heading word; ti, title.
Studies were included if they met the following criteria: (1) all participants were adults aged 18 years or older; (2) inclusion of a group with SSDs (i.e., schizophrenia, schizoaffective disorder, schizophreniform disorder, delusional disorder, brief psychotic disorder, schizotypal or schizoid personality disorder, or psychosis not otherwise specified) or first episode psychosis based on criteria from the Diagnostic and Statistical Manual of Mental Disorders (DSM); (3) study assessed depressive symptoms using a clinical rating measure (e.g., Calgary Depression Scale for Schizophrenia (CDSS) or Hamilton Depression Rating Scale (HAMD)); (4) study utilized one (or more) of the following structural/functional MRI modalities: T1-weighted scans measuring brain morphology (e.g., volume or thickness), diffusion-weighted scans measuring white matter integrity (e.g., FA or MD), or T2*-weighted scans measuring brain function (e.g., activity or connectivity); and (5) study reported findings from an analysis investigating the association between imaging measures and depressive symptoms.
Studies were excluded if they: (1) included participants diagnosed with a major neurological illness (e.g., stroke, Parkinson’s disease, epilepsy, multiple sclerosis, traumatic brain injury); (2) reported on case studies or non-human subjects. Conference abstracts, commentaries, opinion pieces, letters to the editor, and reviews were also excluded. As we conducted the review, we added an additional exclusion criterion to exclude transdiagnostic studies in which SSDs did not constitute at least 75% of the sample, and the effects in SSDs were not reported separately (i.e., the association between an imaging measure and depressive symptoms was observed across multiple diagnoses and did not specify SSDs).
Following the removal of duplicate entries, studies identified through electronic database searches underwent initial screening based on their titles and abstracts. This screening was carried out independently by two reviewers (JG and OC), who assessed the studies for their relevance with regard to the study population, condition, methodology, and outcomes of interest. Any discrepancies between assessments were resolved by a third reviewer (LDO). Subsequently, a full-text review of studies included from the initial screening stage was conducted independently by two reviewers (JG and MTS). In cases where uncertainty regarding eligibility arose, a third reviewer (TM) resolved the discrepancies. A covidence reference management system was used throughout the screening and selection process of the studies.
Data from studies that satisfied the inclusion criteria were extracted and recorded in a database by 1 of 2 reviewers (JG and OC) and subsequently cross-checked by the other. This database encompassed details including bibliographic information, study type, sample size, mean age of the groups, sex distribution, medication usage details, diagnostic criteria or assessment tools for SSDs evaluation, scales or assessments for measuring depressive symptoms, imaging modality, imaging analysis and processing approach, statistical analysis methods, and a summary of study findings.
For assessing the quality and risk of bias in the included articles, a modified version of the Newcastle Ottawa Scale (NOS) for cohort studies was utilized, performed by either JG or OC (see Supplemental Table S1 for details). The questions regarding the ‘non-exposed’ cohort were removed, as we were only interested in SSD-specific findings. Additionally, the scale was modified to check the adequacy of the sample size per group, and a point was given to studies with a sample size of 30 or greater 30 , 31 . Since medication usage is an important confounding factor in the link between depressive symptom severity and brain metrics 32 , 33 , one question was added to assess whether medication information was acquired in the studies. A point was also given to studies that had used a validated clinical scale when assessing depressive symptoms. The modified NOS score ranged from 1 to 8, indicating low to high quality. In summary, points were allocated to each study and summed up to range from 0–8, with scores between 0-3 indicating poor quality; 4–5, moderate quality; and 6+, good quality. Any uncertainties that arose during the assessment were discussed between the two reviewers (JG and OC) until a consensus was reached.
Our initial search identified 5,765 potentially relevant studies, excluding duplicates. Following a review of titles and abstracts, 5570 studies were excluded, leaving 195 for full-text screening. After this stage, 162 studies were excluded, resulting in a final selection of 33 studies. Among these, 14 studies used T1-weighted structural MRI (sMRI) or dMRI, 18 used fMRI, and one study used both fMRI and sMRI (Fig. 2 ). Tables 1 and 2 present the characteristics of the structural and functional neuroimaging studies, respectively, including the number of participants, sex distribution, mean age, and quality assessment scores. Across included studies, sample sizes tended to be small (a group of less than 30 participants in 15 out of 33 studies), yet exhibited a wide variation (overall sample sizes ranged from 15 to 312 participants). Most study participants were male (1293 of 2007; 64%) and had an average age of 33.7 土 11.2. Antipsychotic medication use was reported in 21 studies, with 19 using chlorpromazine, one using olanzapine, and one using haloperidol equivalents; two studies specified that participants were drug or neuroleptic naive. Additionally, six studies reported the use of antidepressant medication. All studies used either DSM-III, DSM-IV, or DSM-5 for SSDs diagnosis (details provided in Tables 1 – 2 ). Thirty-one studies recruited patients with schizophrenia. Six studies included patients with schizoaffective disorder and one with schizophreniform disorder. Four studies designated patients as first-episode schizophrenia or psychosis. None of the studies included individuals with comorbid depressive disorders.
DSM Diagnostic and Statistical Manual of Mental Disorders, dMRI diffusion MRI, fMRI functional magnetic resonance imaging, rs-fMRI resting-state fMRI, sMRI structural MRI, SSDs schizophrenia spectrum disorders.
One study received a low score (<4 points) 34 , 15 studies received a moderate score (4–5 points) 35 , 36 , 37 , 38 , 39 , 40 , 41 , 42 , 43 , 44 , 45 , 46 , 47 , 48 , 49 , and 17 studies received a high score (6+ points) 27 , 50 , 51 , 52 , 53 , 54 , 55 , 56 , 57 , 58 , 59 , 60 , 61 , 62 , 63 , 64 , 65 on the modified NOS. Validation of diagnoses by independent sources was frequently unreported, and additional points were lost relatively uniformly across the other evaluation criteria.
Table 1 provides an overview of the included structural studies, encompassing key details such as the main clinical measure of depressive symptoms, the neuroimaging metric used, and a summary of the study’s findings. Figure 3 summarizes frequently implicated brain regions and white matter tracts.
The color scale corresponds to the frequency of the region or tract reported. A A schematic illustration of regions implicated in depressive symptoms in SSDs. Subcortical regions are shown through a glass brain, and cortical regions are displayed on the cerebral cortex, as per the Desikan-Killiany Cortical Atlas parcellation. Top regions include the bilateral hippocampus, as well as the right frontal areas. Implicated regions are further subdivided into positive ( B ) and negative ( C ) associations with depressive symptoms. D A schematic illustration of tracts implicated in depressive symptoms in SSDs. Tracts are shown overlaid on a glass brain, as per the O’Donnell Research Group Fiber Clustering White Matter Atlas parcellation. CC Corpus Callosum, CR Corona Radiata, sFOF Superior Fronto-Occipital Fasciculus, SLF Superior Longitudinal Fasciculus and ThalR Thalamic Radiation. Top tracts include CR, ThalR, and SLF. Note that association and projection tracts are displayed in the left hemisphere, and only the genus of the CC is shown for clarity. Both dMRI studies found positive correlations between white matter tract integrity and depressive symptoms.
The association between structural neuroimaging metrics with depressive symptoms was assessed using scales such as the CDSS ( n = 4) 27 , 35 , 39 , 64 , the depression-anxiety subscale or depressive factor score of the Positive and Negative Syndrome Scale; PANSS ( n = 3) 36 , 38 , 63 , the depression-anxiety subscale or affect factor score of the Brief Psychiatric Rating Scale; BPRS ( n = 3) 37 , 59 , 62 , the HAMD ( n = 3) 60 , 61 , 65 , and the Maryland Trait and State Depression Scale; MTSD ( n = 1) 58 .
Of the 14 structural studies, 10 employed metrics derived from T1-weighted sMRI such as morphology measurements related to volume, surface area, thickness, and size 27 , 35 , 36 , 37 , 60 , 61 , 62 , 63 , 64 , 65 .
Six of these studies associated depressive symptoms with brain morphology using a regional-specific approach 27 , 36 , 37 , 61 , 62 , 63 . Regions of interest (ROIs) included areas within the prefrontal cortex (namely, the dorsolateral prefrontal cortex (DLPFC) and orbitofrontal cortex) 27 , 61 , the hippocampus 36 , 63 , the amygdala 62 , and the cerebellum 37 . A negative correlation emerged between the severity of depressive symptoms and both volume 61 and thickness 27 within the prefrontal cortex. In the hippocampus, Bossù et al. found a negative association between the severity of depressive symptoms and volume 63 , while Smith et al. reported a positive correlation between depression scores and fissure size; a measure suggestive of abnormal neurodevelopment 36 . In the remaining studies, depression scores were positively associated with amygdalar volume 62 , and negatively associated with cerebellar volume 37 .
Four sMRI studies investigated the relationship between depressive symptoms and brain morphology using a whole-brain approach 35 , 60 , 64 , 65 . Kohler et al. reported increased left temporal lobe volume in patients with high depressive symptoms compared to those with low depressive symptoms 60 , whereas an association of lower volume in the superior frontal and orbitofrontal gyrus with higher depression scores was identified by Siddi et al. 64 . In a multivariate brain-behavior analysis, Buck et al. found specific patterns in females with SSDs, where fewer depressive symptoms were associated with changes in hippocampal subfields and varying thickness in specific cortical regions; such as lower thickness in the right superior temporal gyrus, entorhinal cortex, pars orbitalis, medial orbitofrontal gyrus and cingulate cortex, and high thickness in the left precentral gyrus, paracentral gyrus, cuneus, and lingual gyrus 35 . Notably, this brain-behavior pattern also correlated with fewer negative symptoms, though to a lesser extent. Finally, Wei et al. found that individuals with comorbid depressive symptoms had significantly greater gray matter volume in the left isthmus cingulate and posterior cingulate cortex, as well as increased surface area in the left isthmus cingulate, left superior parietal gyrus, and right cuneus compared to those without depressive symptoms 65 .
Four studies used dMRI to assess the relationships between white matter tract integrity measures (i.e., FA, MD, radial diffusivity (RD), or white matter connectivity) and depressive symptoms in SSDs. Analytical methods across studies were highly heterogeneous. Chiappelli et al. used voxel-wise tract-based spatial statistics (TBSS) 58 , Amodio et al. used probabilistic tractography 38 , Long et al. used both voxel-wise TBSS and ROI probabilistic tractography 39 and Joo et al. used whole-brain tractography 59 . Two of the four studies that used tractography did not find significant associations between alterations in white matter integrity and depressive symptoms in SSDs 38 , 59 . However, Chiappelli et al. found that greater experience of depression, termed ‘trait depression’, was positively linked to both the overall average FA values throughout the brain and FA values specific to four white matter pathways: the corona radiata, thalamic radiation, superior longitudinal fasciculus, and superior frontal-occipital tract 58 . Similarly, Long et al. found that patients with suicidal ideation exhibited elevated FA in several white matter tracts, including the corpus callosum, left anterior corona radiata, left superior corona radiata, and bilateral posterior corona radiata, as well as decreased MD in the splenium of the corpus callosum, bilateral posterior corona radiata, left posterior thalamic radiation and left superior longitudinal fasciculus 39 . However, this finding should be interpreted with caution, as suicidal ideation in psychosis could have multiple etiologies (i.e., delusion content, auditory verbal hallucination) despite being measured using the CDSS.
Table 2 provides an overview of the included functional studies, encompassing key details such as the main clinical measure of depressive symptoms, the neuroimaging metric used, and a summary of the study’s findings. Figure 4 summarizes frequently implicated brain regions and networks, while Supplementary Fig. S5 provides a breakdown based on whether the findings are from resting-state or task-based analyses.
The color scale corresponds to the frequency of the region or network reported. A A schematic illustration of regions implicated in depressive symptoms in SSDs. Subcortical regions are shown through a glass brain, and cortical regions are displayed on the cerebral cortex, as per the Surface-Based Multimodal parcellation. Top regions include the left caudate and putamen and bilateral frontal area. Note that some studies investigated specific regions of interest (ROIs), and did not use a whole-brain approach. Implicated regions are further subdivided into positive ( B ) and negative ( C ) associations with depressive symptoms. D A schematic illustration of networks implicated in depressive symptoms in SSDs. Networks are displayed on the cerebral cortex, as per the Cole-Anticevic Brain-wide Network Partition, AUD Auditory Network, DMN Default Mode Network, FPN Frontoparietal Network, LAN Language Network, SMN Somatomotor Network, SN Salience Network. Networks were reported bilaterally but are displayed on the left hemisphere for clarity. Top network connections include within- DMN, FPN, and SN. All studies found negative correlations between network-based functional connectivity and depressive symptoms. One study identified both negative and positive associations with depressive symptoms (positive association found within-FPN, and between DMN-SMN).
The association between functional neuroimaging metrics with depressive symptoms was assessed using scales such as the depression-anxiety subscale or depressive factor score of PANSS ( n = 6) 34 , 41 , 51 , 52 , 53 , 57 , the CDSS ( n = 5) 40 , 43 , 45 , 47 , 48 , the depression-anxiety subscale or affect factor of BPRS ( n = 3) 54 , 55 , 56 , the Beck’s Depression Inventory; BDI/BDI-II ( n = 3) 44 , 46 , 50 , the MTSD ( n = 1) 42 .
Nine fMRI studies utilized metrics derived from resting-state fMRI (rs-fMRI) data, such as functional connectivity 34 , 40 , 52 , 53 , 54 , 55 , 56 , amplitude of low-frequency fluctuations (ALFF) 57 , and global/network efficiency 41 .
Five of these studies investigated associations of depressive symptoms with brain function using a specific seed- or a-priori network-based approach. In a lower-quality ROI-based analysis of resting state functional connectivity, Xu et al. found no significant correlation between depressive symptoms and the substantia nigra/ventral tegmental area 34 . However, in analyses of resting state functional connectivity based on specific networks of interest, depressive symptoms were linked to the default mode network (DMN) 55 , salience network 40 , 52 , and frontoparietal network (FPN) 53 (often synonymous with the central executive network; CEN).
The remaining four studies used a whole-brain regional or network-level approach 41 , 54 , 56 , 57 . Analytical methods and findings across studies were variable. Li et al. demonstrated that an increase in ALFF, which quantifies the strength of low-frequency brain activity fluctuations, in the dorsolateral region of the superior frontal gyrus was significantly linked to a greater reduction in depression scores 57 . Doucet et al. showed a robust pattern of functional network connectivity strongly correlated with improvements in depressive symptoms, with higher within-DMN connectivity being a significant positive predictor, while reduced within-CEN and diminished connectivity between DMN and sensorimotor networks acted as important negative predictors 56 . Notably, this connectivity pattern also correlated with improvements in positive symptoms. Moreover, Lee et al. found the variance in depressive symptom severity can be explained by within-network connectivity of the salience network and connectivity between salience-language networks and somatomotor-auditory networks 54 . Lastly, Su et al. used graph theoretical analysis of networks to show depression symptoms were significantly correlated with the overall efficiency of brain network information processing 41 .
Nine studies employed task-based fMRI to evaluate the relationship between functional brain activity and depressive symptoms in SSDs 42 , 43 , 44 , 45 , 46 , 47 , 48 , 50 , 51 ; three of which investigated specific ROIs. Significant positive associations were found between functional activity in the ventral striatum during a monetary incentive delay task measuring reward processing 43 , 48 , and visual-related regions during an object perception task 45 with depressive symptoms.
The remaining six studies used a whole-brain approach 42 , 44 , 46 , 47 , 50 , 51 . Two of the studies did not find any significant associations between brain activation and depressive symptoms 50 , 51 . Conversely, Lee et al. found that activity in the left posterior cingulate cortex was inversely correlated with overall depression scores 47 . Arrondo et al. demonstrated a negative correlation between depression severity and ventral striatum activity during reward anticipation 46 . Kumari et al. highlighted significant positive correlations between depression scores and brain activity in several regions while processing fearful expressions, including the left thalamus, para post-pre-central gyrus, putamen-globus pallidus, supramarginal gyrus, insula, inferior-middle frontal gyrus, and right superior frontal gyrus, extending to other frontal and cingulate gyri 44 . Moreover, higher activity was noted in thalamic and superior frontal gyrus clusters among patients with moderate-to-severe depression compared to those with milder levels of depression. Lastly, Kvarta et al. found a significant inverse correlation between anticipatory threat-induced ventral anterior cingulate cortex cluster activation and trait depression 42 .
A study with the largest sample size ( n = 312) by Liang et al., employed a multimodal approach investigating both whole-brain fractional ALFF (fALFF) and gray matter volume in relation to depressive symptoms, assessed using the Montgomery-Asberg Depression Rating Scale (MADRS) (42). The authors investigated associations in schizophrenia and schizoaffective disorder groups separately and identified distinctions. In schizophrenia, elevated depression scores were linked to increased fALFF in the thalamus and hippocampus, as well as heightened gray matter volume in the insula and inferior frontal cortex. In schizoaffective disorder, higher depression scores were associated with increased fALFF and greater gray matter volume in the lingual and frontal gyrus.
We conducted a systematic review of 33 studies, comprising 14 structural MRI studies (10 sMRI and four dMRI), 18 fMRI studies, and one study analyzing both sMRI and fMRI, aiming to provide a comprehensive summary of the current neuroimaging research regarding depressive symptoms in individuals with SSDs. Our review underscored a notable gap in the literature, revealing a substantial lack of studies investigating the neurobiology of depression in SSDs. The relatively few studies that did explore imaging metrics of depressive symptoms demonstrated high variability and limited consistency across implicated neural correlates. These studies employed a diverse range of scales or assessments to measure depressive symptoms, an array of imaging modalities, and variable approaches to imaging analysis and statistical methods, posing a challenge for interpretation. For instance, regions that appeared more prominently in task-based fMRI studies versus resting-state (e.g., striatum) likely reflect the influence of emotional stimuli, activating areas involved in processing affective information, thus introducing potential biases. Nevertheless, findings delineated subcortical regions, specifically the striatum, thalamus, and hippocampus, as well as frontal regions as potentially implicated in the manifestation of depressive symptoms in SSDs. Notably, many of these correlates showed contrasting associations with depression across studies, which may be attributed to studies focusing on larger-scale brain areas, potentially overlooking nuances of sub-regions.
The subcortical and frontal areas highlighted in this review align with the results of several fMRI/MRI studies of MDD, consistently noting atypical morphology and functioning of such regions 66 . It has been suggested that these regions may be acting as central brain “hubs”, where impairments could lead to key symptomatology as observed in MDD (see Zhang et al. 2018, for an in-depth review) 66 . The involvement of the cortico-striatal-thalamo-cortical circuit in both SSDs 67 , 68 and severe mood disorders, including MDD 69 , supports the notion that common abnormalities in these regions could reflect an overlapping feature of mood-related symptoms across diagnoses 70 . However, confidence in this shared neurobiology is constrained by methodological limitations in the literature.
A major challenge arises from the variation in scales and inclusion criteria used across studies to either identify patients with depressive symptoms or report on the severity of depression symptoms in SSDs. The studies identified in this review used a variety of tools to assess depressive symptoms in SSDs, with some originally developed for MDD and others for SSDs. A few studies classified patients as having depression with symptoms above a specified symptom scale cut-off, while no studies included or reported information regarding comorbid depressive disorders. When reporting depression severity, all studies reported an average total depression score and did not take into account specific symptoms that might be more relevant to SSDs. Prior work has suggested depressive symptoms in SSDs can be broken down into two dimensions: depression-hopelessness and pathological guilt 71 which may have distinctive neural circuitry and treatment outcomes (Gallucci et al., accepted). Differentiation of these factors could unveil more consistent and clinically meaningful distinctions, emphasizing the importance of future research considering these separate dimensions rather than focusing on total depression scores. This approach could also provide insight into more general depressive symptoms in individuals with SSDs who might not fulfill the criteria for depressive disorders like MDD.
Another knowledge gap lies in understanding the extent to which negative symptoms may contribute to the overall picture of depressive symptoms. Many of the brain regions associated with depressive symptoms in our review have also been implicated in negative symptoms of SSD, such as structural brain abnormalities in the frontal and subcortical areas, along with functional alterations concentrated in the thalamocortical circuits 72 . Lako et al. have argued that depression scales designed for MDD may not effectively distinguish depressive symptoms from negative symptoms in SSDs, limiting our ability to adequately characterize these clinical phenotypes 73 . This conceptual overlap may contribute to heterogeneity seen across studies’ findings 11 , 74 . Our recent work, employing an advanced multivariate correlation approach, demonstrated distinct neural circuitry underlying depressive and negative symptoms (Gallucci et al., accepted). This provides evidence that these symptoms are separable constructs with differing neurobiological underpinnings. Further, brain stimulation treatments, such as rTMS targeting the DLPFC, have yielded substantial effects in mitigating depressive symptoms in MDD 26 , and preliminary support in SSDs 27 . This intervention has also demonstrated promising yet inconsistent efficacy in ameliorating negative symptoms in SSDs, suggesting potentially shared yet distinct pathophysiological mechanisms 75 , 76 .
Further limitations in the literature which significantly impacted interpretability should be acknowledged. There were considerable variations in the samples being studied, such as age, sex ratio, medication usage, and stage of illness (i.e., chronic versus first-episode). Greater attention should be devoted to examining subgroups within SSDs, such as first-episode patients or those who are drug-naive. A critical constraint across nearly all studies was the insufficient consideration for potential confounding factors, i.e., negative symptoms, as alluded to above. Notably, a large portion of relevant studies (23 out of 34) investigated depressive symptoms as secondary exploratory or post hoc analyses, lacking an SSD sample prospectively enriched with individuals experiencing depressive symptoms. This emphasizes the pressing need for more direct studies prioritizing the recruitment of such individuals, enabling a more nuanced examination of the underlying neurobiology.
In our systematic review, we identified 33 studies focusing on neuroimaging research related to depressive symptoms in individuals with SSDs. We noted considerable variability and a lack of consistency amongst neural correlates. This heterogeneity may derive from assessment scales that fail to adequately distinguish between subdimensions of depressive symptoms. Our findings also suggest potential shared neurobiological underpinnings among depressive symptoms in SSDs and MDD. Given the relative scarcity of neuroimaging studies on depressive symptoms in SSDs and their inconsistent results, there is a clear need for research focused on directly investigating the neurobiology of depression in SSDs. Future studies may benefit from considering a more fine-grained and disorder-specific assessment of depressive symptoms in SSDs, rather than ‘total depression’ summary scores. Lastly, in light of preliminary evidence suggesting some neurobiological overlap between depressive symptoms in SSDs and MDD, a potential future direction may be to examine both unique and shared neural correlates across the two disorders. Exploring the neurobiology of individuals with SSDs and comorbid MDD is a severely understudied yet valuable avenue of research. While prior studies on MDD have noted irregularities in white matter tracts 77 and brain networks 78 , we lack sufficient evidence to comment on how these abnormalities may relate to depressive symptoms in SSDs. The limited availability of studies using dMRI metrics or examining brain function at the network level underscores the necessity for further investigation. A better understanding of the neural correlates linked to depressive symptoms in SSDs could have pronounced implications, informing innovative treatment strategies tailored to alleviating depression specifically within SSDs, in contrast to the conventional but ineffective methods that were developed for MDD 11 , 12 , 13 .
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These authors contributed equally: Aristotle N. Voineskos, Colin Hawco.
Campbell Family Mental Health Research Institute, Toronto, ON, Canada
Julia Gallucci, Maria T. Secara, Lindsay D. Oliver, Brett D. M. Jones, Tulip Marawi, George Foussias, Aristotle N. Voineskos & Colin Hawco
Institute of Medical Science, University of Toronto, Toronto, ON, Canada
Julia Gallucci, Maria T. Secara, Oliver Chen, Brett D. M. Jones, Tulip Marawi, George Foussias, Aristotle N. Voineskos & Colin Hawco
Department of Psychiatry, University of Toronto, Toronto, ON, Canada
Lindsay D. Oliver, Brett D. M. Jones, George Foussias, Aristotle N. Voineskos & Colin Hawco
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J.G. substantially contributed to the conception or design of the work, acquisition, analysis, and interpretation of the data, drafting the manuscript and revising it, and agreeing to be accountable for all aspects of the work. M.T.S and O.C. substantially contributed to the acquisition of the data. L.D.O., B.J., T.M., and G.F. contributed to drafting the manuscript. C.H. and A.N.V. substantially contributed to the conception or design of the work and interpretation of the data, drafting the manuscript and revising it, providing formal supervision for all aspects of the work, and agreeing to be accountable for all aspects of the work.
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Gallucci, J., Secara, M.T., Chen, O. et al. A systematic review of structural and functional magnetic resonance imaging studies on the neurobiology of depressive symptoms in schizophrenia spectrum disorders. Schizophr 10 , 59 (2024). https://doi.org/10.1038/s41537-024-00478-w
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Adaptability analysis of integrated project delivery method in large- and medium-sized engineering projects: a fahp-based modeling solution.
2. development of the ipd method, 2.1. research trends of project management, 2.2. development of the ipd method, 2.2.1. introduction of the ipd method.
2.2.3. integration of ipd and other methods, 2.2.4. research necessity of the ipd method in engineering projects, 3. modeling methods, 3.1. fahp-based evaluation indicators, 3.1.1. a brief description of fahp theory, 3.1.2. fahp-based indicators.
3.3. decision-making score evaluation method, 4. results and case application, 4.1. mathematical expressions for ipd adaptability, 4.2. case application, 4.2.1. description of the case project, 4.2.2. application of the ipd method, 4.2.3. comprehensive benefit analysis between the ipd method and or method, 4.3. limitations and future directions, 4.3.1. contributions, 4.3.2. limitations, 4.3.3. future directions, 5. conclusions, author contributions, data availability statement, acknowledgments, conflicts of interest, abbreviations.
IPD | Integrated Project Delivery |
FAHP | Fuzzy Analytic Hierarchy Process |
DBB | Design–Bid–Build |
DB | Design–Build |
CM at Risk | Construction Manager at Risk |
BOT | Build–Operate–Transfer |
EPC | Engineering Procurement Construction |
OR | Owner’s Representative |
OCM | Owner’s Construction Management |
PPP | Public–Private Partnerships |
AHP | Analytic Hierarchy Process |
DC | Development Cost |
PCC | Purchase Cost |
PDC | Production Cost |
SC | Selling Cost |
SR | Schedule Risk |
QR | Quality Risk |
PR | People Risk |
CR | Cost Risk |
QM | Quality Management |
IM | Investment Management |
HRM | Human Resources Management |
HSEM | Health, Safety, and Environment Management |
CM | Communication Management |
IP | Initiation Phase |
EP | Exploration Phase |
CP | Construction Phase |
AP | Acceptance Phase |
OMP | Operation and Maintenance Phase |
Click here to enlarge figure
Target Level | Criterion Level | |||||
---|---|---|---|---|---|---|
Cost control | Process control | Management control | Schedule control | |||
Cost control | 0.5 | |||||
Risk control | 0.5 | |||||
Management control | 0.5 | |||||
Schedule control | 0.5 | |||||
Cost control | DC | PCC | PDC | SC | ||
DC | 0.5 | |||||
PCC | 0.5 | |||||
PDC | 0.5 | |||||
SC | 0.5 | |||||
Risk control | SR | QR | PR | CR | ||
SR | 0.5 | |||||
QR | 0.5 | |||||
PR | 0.5 | |||||
CR | 0.5 | |||||
Management control | QM | IM | HRM | HSEM | CM | |
QM | 0.5 | |||||
IM | 0.5 | |||||
HRM | 0.5 | |||||
HSEM | 0.5 | |||||
CM | 0.5 | |||||
Schedule control | IP | EP | CP | AP | OMP | |
IP | 0.5 | |||||
EP | 0.5 | |||||
CP | 0.5 | |||||
AP | 0.5 | |||||
OMP | 0.5 |
Indicators | Weighting Calculation | Scale |
---|---|---|
3.60 | ||
3.71 | ||
3.10 | ||
3.37 | ||
3.46 |
The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content. |
He, H.; Gan, X.; Liu, L.; Zhang, X. Adaptability Analysis of Integrated Project Delivery Method in Large- and Medium-Sized Engineering Projects: A FAHP-Based Modeling Solution. Buildings 2024 , 14 , 1999. https://doi.org/10.3390/buildings14071999
He H, Gan X, Liu L, Zhang X. Adaptability Analysis of Integrated Project Delivery Method in Large- and Medium-Sized Engineering Projects: A FAHP-Based Modeling Solution. Buildings . 2024; 14(7):1999. https://doi.org/10.3390/buildings14071999
He, Huiyu, Xiwei Gan, Lin Liu, and Xing Zhang. 2024. "Adaptability Analysis of Integrated Project Delivery Method in Large- and Medium-Sized Engineering Projects: A FAHP-Based Modeling Solution" Buildings 14, no. 7: 1999. https://doi.org/10.3390/buildings14071999
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This study investigated factors that predict the acceptance of metaverse applications for educational usage among university students from the facet of the Technology Acceptance Model. As both the metaverse and the Technology Acceptance Model gained popularity, little attention was paid to the metaverse’s acceptance and the factors that led to the metaverse’s acceptance from the Technology Acceptance Model’s tenets. This creates a gap in our existing understanding of the metaverse. To fill the gap, Future Learning Intention (FLI), Technology Optimism (TO), Hedonic Motivation (HM), Perceived Enjoyment (PE), Technology Trust (TT), and Anticipated Benefits (AB) were integrated into the Technology Acceptance Model as external variables to study the acceptance of the metaverse among university students. The extended Technology Acceptance Model consists of 18 hypotheses that were tested using the Structural Equation Model and Mediation Analysis with data from 215 university students. The model developed was found to accurately determine university students’ acceptance of metaverse applications. FLI and TT were significant predictors of usefulness, while FLI, TT, and AB were significant antecedents of ease of use, according to the model. The samples’ Attitudes Toward Using (AT) mediated the relationship between Perceived Usefulness (PU) and Perceived Ease of Use (PEU) toward the students’ Behavioural Intention (BI) to use the metaverse. Suggestions for educational practise and metaverse development were highlighted for the metaverse’s future development in both educational and non-educational contexts. Future development of metaverse applications should prioritise understanding their prospective users’ characteristics while still maintaining the applications’ usefulness and ease of use.
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School of Education, Faculty of Social Sciences and Humanities, Universiti Teknologi Malaysia, 81310, Johor Bahru, Malaysia
Mohd Shafie Rosli
Department of Social Science, Centre for General Studies and Co-Curricular, Universiti Tun Hussein Onn Malaysia, 86400, Batu Pahat, Malaysia
Nor Shela Saleh
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Conceptualization: Mohd Shafie Rosli; Methodology: Nor Shela Saleh; Formal analysis and investigation: Mohd Shafie Rosli, Nor Shela Saleh; Writing – original draft preparation: Mohd Shafie Rosli; Writing – review and editing: Nor Shela Saleh.
Correspondence to Mohd Shafie Rosli .
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Rosli, M.S., Saleh, N.S. Predicting the Acceptance of Metaverse for Educational Purposes in Universities: A Structural Equation Model and Mediation Analysis of the Extended Technology Acceptance Model. SN COMPUT. SCI. 5 , 688 (2024). https://doi.org/10.1007/s42979-024-03015-9
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DOI : https://doi.org/10.1007/s42979-024-03015-9
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