An adaptive AI-based virtual reality sports system for adolescents with excess body weight: a randomized controlled trial.
Wang J, Qin Y, Wu Q, Zeng D, Gao X, Wang Q, Li Z, Ni Y, Li H, Zhang P, Guo J, Ma W, Maitusun M, Jin X, Chen M, Zhu L, Lu Q, Chen Q, Wu Y, Lin C, Han R, Cheng D, Ni J, Wang X, Yao F, Zhuang J, Xia J, Liu D, Lu Y, Kang P, Yu S, Chen A, Zhang Y, Li Q, Ge W, Long X, Jiang Z, Guan Z, Jin Z, Jin P, Li T, Shu J, Yang J, Wang J, Jiang N, Qian J, Jung Y, Zhang H, Yang Q, Ma L, Wu X, Huang X, Si D, Ren J, Qiao H, Guo Y, Huang Z, Wang W, Deng W, Bi L, Zhao D, Li Y, Lau RWH, Tham YC, Ma X, Ma J, Shen D, Zhang S, Guan H, Zou W, Guo M, Guan X, Yang X, Xu A, Wu J, Panagiotou G, Tse MA, Kim J, Wu E, Thalmann D, Thalmann NM, Fregni F, Wong TY, Jia W, Zeng R, Lim CT, Sheng B, Li H
- DOI
- 10.1038/s41591-025-03724-5
- Record issued
- 2026-08-15
- Engine
- 7.39.0
- Exported
- 2026-09-22
Prepared by Alpha1. This document is confidential: it is intended for the recipient it was shared with and must not be redistributed. The live record at alpha1science.com/verify/9af8caea-df6a-41d0-8685-907f99b1b701 is authoritative.
How this rating was calculated
- IntegrityIntegrity concern ×2−1★
- ClaimsEfficacy rests on an unvalidated surrogate endpoint−0.5★
- ClaimsTreatment effect not shown to be clinically meaningful−0.5★
- ReportingEthical approvals partially met−0.25★
- CitationsUnresolved reference−0.25★
- 01Efficacy rests on an unvalidated surrogate endpoint
The primary efficacy claim is reduction in fat mass, which is a surrogate marker for obesity-related health outcomes. The paper does not demonstrate target engagement at the tested dose (e.g., PK/PD) nor cite validated evidence linking fat mass reduction to hard clinical outcomes in this context. Additionally, cognitive improvements are based on surrogate measures (olfactory tests, working memory tasks) without established clinical significance.
“REVERIE sports intervention was effective in reducing primary outcome fat mass (mean −4.28 kg (95% confidence interval (CI) −6.35 to −2.22), relative to control)”
- 02Treatment effect not shown to be clinically meaningful
The primary effect size is a reduction in fat mass of 4.28 kg relative to control, but no anchor to clinical meaningfulness (e.g., minimal clinically important difference) is provided. The cognitive improvements (e.g., 2-back accuracy increase of 10.88%) are presented without established clinical significance.
“REVERIE sports intervention was effective in reducing primary outcome fat mass (mean −4.28 kg (95% confidence interval (CI) −6.35 to −2.22), relative to control)”
This Kaimen Rigor review uses Kaimen Rigor reviewers trained on a curated corpus of high-fidelity and retracted papers, with expert supervision and curation. It can still make mistakes; verify each finding against the source before relying on it.
This is a well-conducted and transparently reported RCT of a VR sports intervention in adolescents with excess body weight, with strong reporting of methods, biological variables, statistical analysis, and data/code availability. The main weakness is the absence of an explicit ethics approval statement in the main text, along with minor reporting gaps in randomization method, blinding, and outlier handling.
Both reviewers classified the study as interventional (RCT), and this was adopted. The evaluation covered all eight dimensions; several sub-criteria were marked not applicable (e.g., species/strain, housing, antibodies, cell lines) as expected for a human device trial. The reviewers diverged on ethical approvals (warn vs. pass), and the synthesized status is warn based on the missing explicit ethics statement. The statistics verification recomputed only 2 tests (both consistent); the rest of the statistical results remain unverified.
Numerical inconsistencies
1 finding · worst lowValues that contradict each other or are impossible for the stated sample: recomputed p-values and test statistics, GRIM/GRIMMER checks on summary numbers, percentages against their own counts, totals against their parts, and estimates against their own confidence intervals.
- Internal contradictions in the reported numbersAssessed
Recomputed 2 tests: 2 consistent, 0 inconsistent; 2 via agent-written checks.
- CONSISTENTreported p < .001 · recomputed p = <.001Reviewers 1, 2Primary outcome fat mass change: REVERIE vs control
“REVERIE sports intervention was effective in reducing primary outcome fat mass (mean −4.28 kg (95% confidence interval (CI) −6.35 to −2.22), relative to control)”
Taken as given: The estimate is the mean difference in fat mass change between REVERIE and control.; The 95% CI is two-sided.; The p-value is two-sided.Method: Recomputed p-value from the reported mean difference and 95% CI using the normal approximation.How we recomputed it: pCI(-4.28, -6.35, -2.22, 0) - CONSISTENTreported p < .001 · recomputed p = <.001Reviewers 1, 2Primary outcome fat mass change: Physical vs control
“with no significant difference compared with physical sports (mean −5.06 kg (95% CI −7.13 to −2.98), relative to control)”
Taken as given: The estimate is the mean difference in fat mass change between Physical and control.; The 95% CI is two-sided.; The p-value is two-sided.Method: Recomputed p-value from the reported mean difference and 95% CI using the normal approximation.How we recomputed it: pCI(-5.06, -7.13, -2.98, 0)
- lowinternal contradictionThe abstract reports 227 participants, but the Methods state 240 enrolled. The difference is likely due to exclusions, but the CONSORT diagram is not fully visible.
involving 227 adolescents with excess body weight ( n = 227). ... a total of 240 adolescents with excess body weight ... were enrolled
Abstractreviewer’s wording
Overstated conclusions
3 findings · worst highConclusions that reach past what the paper's own results support — including a significance claim that no longer holds when the statistic is recomputed, and efficacy resting on an unvalidated surrogate endpoint.
- Efficacy rests on an unvalidated surrogate endpointAssessed
- Treatment effect not shown to be clinically meaningfulAssessed
- Conclusions only partially backed by the presented evidenceAssessed
9 major claims checked against the paper's own evidence: 4 only partially supported (evidence backs part of the claim; gaps or caveats remain); the rest adequately supported.
- partialReviewer 1REVERIE sports improved cognitive function beyond physical sports.Exploratory analyses show improvements in olfactory and working memory tasks, but these were not pre-specified and multiple testing was not adjusted.Evidence: Table 2: TDI score mean 2.84 (95% CI 1.15 to 4.53) and 2-back accuracy mean 10.88% (95% CI 1.19% to 20.56%) for REVERIE vs physical.
“REVERIE sports demonstrated superior cognitive enhancements compared to physical sports in exploratory analyses”
AbstractFind in source - partialReviewer 1REVERIE sports enhanced neural efficiency and neuroplasticity.fMRI findings show changes in brain activation and connectivity, but the clinical significance and direct link to cognitive improvement are not fully established.Evidence: fMRI results show significant group-by-time interactions and connectivity changes.
“Functional magnetic resonance imaging exhibited that REVERIE sports enhanced neural efficiency and neuroplasticity.”
ResultsFind in source - partialReviewers 1, 2Multi-omics analyses revealed distinct changes induced by REVERIE sports associated with cognitive improvement.Multi-omics changes are reported, but the association with cognitive improvement is correlational and exploratory.Evidence: Multi-omics profiling showed significant changes in REVERIE group, and correlation networks with brain regions.
“Multi-omics analyses revealed distinct changes induced by REVERIE sports that were closely associated with cognitive improvement.”
ResultsFind in source - partialReviewer 2REVERIE sports demonstrated superior cognitive enhancements compared to physical sports in exploratory analyses.The claim is supported by exploratory analyses showing significant improvements in olfactory TDI score and 2-back accuracy, but these are labeled as exploratory and not adjusted for multiple testing.Evidence: Table 2: 'TDI score: mean 2.84 (95% CI 1.15 to 4.53)' and '2-back accuracy: mean 10.88% (95% CI 1.19% to 20.56%)'
“REVERIE sports demonstrated superior cognitive enhancements compared to physical sports in exploratory analyses, as evidenced by olfactory tests (total score: mean 2.84 (95% CI 1.15 to 4.53)) and working memory paradigm (2-back accuracy: mean 10.88% (95% CI 1.19% to 20.56%))”
AbstractFind in source - supportedReviewer 1REVERIE sports intervention reduced fat mass compared to control.The primary outcome analysis shows a significant reduction in fat mass with a 95% CI excluding zero.Evidence: Table 2: FM change -3.15 kg (95% CI -4.29 to -2.01) for REVERIE vs control, P<0.001.
“REVERIE sports intervention was effective in reducing primary outcome fat mass (mean −4.28 kg (95% confidence interval (CI) −6.35 to −2.22), relative to control)”
AbstractFind in source - supportedReviewer 1REVERIE sports showed no significant difference compared to physical sports for fat mass.The comparison between REVERIE and physical sports for fat mass was not significant (P=0.274).Evidence: Table 2: P value d = 0.274 for FM.
P value d | 0.274
Table 2reviewer’s wording - supportedReviewer 2REVERIE sports intervention was effective in reducing primary outcome fat mass relative to control.The claim is supported by the primary analysis showing a mean reduction of -4.28 kg (95% CI -6.35 to -2.22, P<0.001) relative to control.Evidence: Table 2 and Abstract: 'REVERIE sports intervention was effective in reducing primary outcome fat mass (mean −4.28 kg (95% confidence interval (CI) −6.35 to −2.22), relative to control)'
“REVERIE sports intervention was effective in reducing primary outcome fat mass (mean −4.28 kg (95% confidence interval (CI) −6.35 to −2.22), relative to control)”
AbstractFind in source - supportedReviewer 2REVERIE sports showed improvements in physical fitness, psychological well-being and sports willingness after 8-week intervention, which remained at 6-month follow-up.The claim is supported by Table 2 and Extended Data Fig. 4 showing significant improvements in multiple outcomes at 8 weeks and sustained effects at 6 months.Evidence: Table 2 and Extended Data Fig. 4: 'At a 6-month follow-up after the end of the intervention, the REVERIE sports group maintained significant improvements in standing long jump performance, self-efficacy, self-esteem, well-being, sleeping quality, eating behavior and sports willingness compared to the physical sports group'
“At a 6-month follow-up after the end of the intervention, the REVERIE sports group maintained significant improvements in standing long jump performance, self-efficacy, self-esteem, well-being, sleeping quality, eating behavior and sports willingness compared to the physical sports group”
Results ¶5Find in source - supportedReviewer 2Minimal injury rates were 7.69% for REVERIE and 13.48% for physical sports, with no serious adverse events.The claim is supported by the reported injury rates and the statement that no serious adverse events occurred.Evidence: Results: 'Minimal injuries were reported in 7 (7.69%) participants in the REVERIE group and 12 (13.48%) participants in the physical sports group. No serious adverse events were reported.'
“Minimal injuries were reported in 7 (7.69%) participants in the REVERIE group and 12 (13.48%) participants in the physical sports group. No serious adverse events were reported.”
Results ¶1Find in source
Premise concern: surrogate not validated for clinical benefit; effect size not shown to be clinically meaningful.
- INADEQUATESurrogate endpointThe primary efficacy claim is reduction in fat mass, which is a surrogate marker for obesity-related health outcomes. The paper does not demonstrate target engagement at the tested dose (e.g., PK/PD) nor cite validated evidence linking fat mass reduction to hard clinical outcomes in this context. Additionally, cognitive improvements are based on surrogate measures (olfactory tests, working memory tasks) without established clinical significance.
“REVERIE sports intervention was effective in reducing primary outcome fat mass (mean −4.28 kg (95% confidence interval (CI) −6.35 to −2.22), relative to control)”
- INADEQUATEEffect sizeThe primary effect size is a reduction in fat mass of 4.28 kg relative to control, but no anchor to clinical meaningfulness (e.g., minimal clinically important difference) is provided. The cognitive improvements (e.g., 2-back accuracy increase of 10.88%) are presented without established clinical significance.
“REVERIE sports intervention was effective in reducing primary outcome fat mass (mean −4.28 kg (95% confidence interval (CI) −6.35 to −2.22), relative to control)”
Data authenticity concerns
1 finding · worst lowAn adversarial read for patterns associated with data that may not be genuine: results that look too clean, implausibly large effects, duplicated data or images, and methods that do not match the results reported.
- Data look implausibly cleanAssessed
2 integrity concerns flagged (0 high).
- lowdata too cleanBaseline characteristics appear very well balanced across groups, which is plausible but may warrant scrutiny.
“Baseline characteristics of participants were balanced across groups (Table ).”
Table 1Find in source
Reporting gaps
1 finding · worst mediumRequired detail the manuscript never states — study design, biological variables, ethics approval and consent, key resources, statistical reporting, data and code availability, and overall transparency.
- Ethics/consent reporting incompleteAssessed
The introduction cites multiple references on the global obesity crisis, cognitive risks, and limitations of existing VR systems. It explicitly states the gaps: 'most existing VR sports systems offer one-size-fits-all experiences' and 'there are few rigorous randomized controlled trials (RCTs) validating the effectiveness of VR therapy.' The study objectives follow logically from these gaps. Limitations of prior research are addressed by the design of the RCT and the adaptive AI system.
The paper reports a 1:1:1:1:1 randomization to five groups (physical table tennis, physical soccer, REVERIE table tennis, REVERIE soccer, control). Randomization method is not explicitly described (e.g., computer-generated sequence), but the trial is registered and baseline characteristics are balanced. Blinding is not mentioned for participants or assessors, which is typical for behavioral interventions. A power analysis is referenced in the protocol (ref 13). Inclusion/exclusion criteria are stated: 'adolescents with excess body weight (mean age 14.24 ± 1.77 years; 162 boys, 78 girls) who met the eligibility criteria.' The control group is appropriate. Outlier handling and independent replication are not reported, but these are not standard requirements for a human RCT.
“Clinical Trial registration: ChiCTR2300068786”
“Participants were randomized (1:1:1:1:1) to physical table tennis, physical soccer, REVERIE table tennis, REVERIE soccer or control.”
“From 1 March 2023 to 1 May 2023, a total of 240 adolescents with excess body weight (mean age 14.24 ± 1.77 years; 162 boys, 78 girls) who met the eligibility criteria were enrolled in our study”
Table 1 reports sex (male %), age (mean ± SD), body weight, BMI, and other health metrics. Demographics include age, sex, and baseline clinical characteristics. Sex is reported for all groups, and both sexes are included, so sex_justified is not applicable. Age, weight, and health status are comprehensively reported. Species/strain and housing conditions are not applicable for a human trial.
“Sex (male, %) | 28 (59.54%) | 65 (73.03%) | 58 (63.74%)”
“Age (year) | 14.17 ± 1.85 | 14.15 ± 1.85 | 13.98 ± 1.77”
“Sex (male, %) | 28 (59.54%) | 65 (73.03%) | 58 (63.74%)”
“Age (year) | 14.17 ± 1.85 | 14.15 ± 1.85 | 13.98 ± 1.77”
“Body weight (kg) | 80.24 ± 16.67 | 76.23 ± 16.84 | 75.64 ± 13.25”
The paper does not mention an IRB or ethics committee approval in the main text. Informed consent is not described. Regulatory compliance is not explicitly stated. However, the trial is registered (ChiCTR2300068786) and the protocol is referenced, which may contain ethics details. The absence of an explicit ethics statement in the main text is a reporting gap.
“Clinical Trial registration: ChiCTR2300068786”
“Clinical Trial registration: ChiCTR2300068786”
“Individual-level participant data are not publicly available but can be made accessible by obtaining informed consent from the Data Management Committee of the institution.”
The REVERIE system is described in detail, including hardware (Oculus Quest 2) and software. Software tools are identified (e.g., SPM12, MATLAB, R). Antibodies, cell lines, and mycoplasma testing are not applicable. Organisms are not applicable. Reagents are not applicable as this is a device-based intervention.
“The hardware component includes the Oculus Quest 2 and the table tennis bracket, and to ensure that adolescents with excess body weight can comfortably wear VR devices while maintaining high-quality data collection for sports, we designed and performed three-dimensional (3D) printing of a custom soccer bracket for each participant.”
“fMRI data were analyzed by Statistical Parametric Mapping 12 (SPM12, Welcome Trust Center for Neuroimaging, United Kingdom; http://www.fil.ion.ucl.ac.uk/spm ) under the MATLAB 2021b (The MathWorks Inc.) environment.”
“Statistical analysis of multi-omics data in this study was performed using R language (version 4.2.1, https://www.R-project.org/ ).”
Tests are named (e.g., ANCOVA, linear mixed model, paired t-test). Assumptions are not explicitly verified but standard methods are used. Exact p-values are reported for many outcomes. Effect sizes with CIs are reported. Software is identified. Data presentation includes per-group n and box plots. Mathematical plausibility is not applicable for large-N continuous outcomes.
“FM (kg) | 1.13 (−0.62, 2.88) | −3.92 (−4.87, −2.98) | −3.15 (−4.29, −2.01)”
“P values for outcomes assessed at baseline and the end of intervention were analyzed using a two-sided analysis of covariance (ANCOVA) followed by a Fisher’s least significant difference (LSD) post hoc test, with baseline variable levels included as covariates.”
“FM (kg) | 1.13 (−0.62, 2.88) | −3.92 (−4.87, −2.98) | −3.15 (−4.29, −2.01)”
Data availability statement is detailed, describing managed access for individual participant data and providing accession numbers for omics data. Code is available on GitHub. Repository deposits are present for omics data.
“Individual-level participant data are not publicly available but can be made accessible by obtaining informed consent from the Data Management Committee of the institution.”
“The raw lipidomics, metabolomics and proteomics data generated during this study are available at The National Omics Data Encyclopedia under accession OEP005446”
“REVERIE system source code and demo videos are available at https://github.com/LittleQBerry/REVERIE-Sports”
“Individual-level participant data are not publicly available but can be made accessible by obtaining informed consent from the Data Management Committee of the institution.”
“The raw lipidomics, metabolomics and proteomics data generated during this study are available at The National Omics Data Encyclopedia under accession OEP005446”
“REVERIE system source code and demo videos are available at https://github.com/LittleQBerry/REVERIE-Sports”
Methods are comprehensive, including system development, RCT design, and statistical analysis. Trial registration is provided (ChiCTR2300068786). A CONSORT diagram is included (Fig. 1). Limitations are discussed in the context of the study (e.g., 'Minimal injury rates were 7.69% for REVERIE and 13.48% for physical sports'). Conclusions are proportional, noting that REVERIE 'holds promise' and 'may suggest underlying mechanisms.' Funding sources and competing interests are declared. A reporting guideline (CONSORT) is implicitly followed via the diagram.
“Clinical Trial registration: ChiCTR2300068786”
“Fig. 1 CONSORT diagram.”
“This study was funded by the National Key R&D Program of China (grant no. 2023YFC3305804)”
“Clinical Trial registration: ChiCTR2300068786”
“Fig. 1 CONSORT diagram. Study flow diagram.”
Registered (1 ID: Chinese Clinical Trial Registry). Reporting guideline cited: CONSORT.
Broken references and links
1 finding · worst lowReferences checked against Crossref, OpenAlex and Retraction Watch for retractions and resolvability, plus declared data and code links probed for whether they resolve to content matching the paper.
- References not resolvable to a published paperRecomputed
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- NO DOIField-based fitness assessment in young people: the ALPHA health-related fitness test battery for children and adolescentsNo DOI in the reference — shown for manual review; not independently verifiable (not a fabrication signal).
- NO DOIFitness Measures and Health Outcomes in YouthNo DOI in the reference — shown for manual review; not independently verifiable (not a fabrication signal).
- NO DOIThe Youth Fitness International Test (YFIT) battery for monitoring and surveillance among children and adolescents: a modified Delphi consensus project with 169 experts from 50 countries and territoriesNo DOI in the reference — shown for manual review; not independently verifiable (not a fabrication signal).
- NO DOIDevelopment of the Chinese Smell Identification TestNo DOI in the reference — shown for manual review; not independently verifiable (not a fabrication signal).
- NO DOIProteomics identifies new therapeutic targets of early-stage hepatocellular carcinomaNo DOI in the reference — shown for manual review; not independently verifiable (not a fabrication signal).
- NO DOIControlling the false discovery rate: a practical and powerful approach to multiple testingNo DOI in the reference — shown for manual review; not independently verifiable (not a fabrication signal).
- NO DOIMICE: multivariate imputation by chained equations in RNo DOI in the reference — shown for manual review; not independently verifiable (not a fabrication signal).
- NO DOIPsychophysiological and modulatory interactions in neuroimagingNo DOI in the reference — shown for manual review; not independently verifiable (not a fabrication signal).
4 data/code links checked; 4 live.
- datahttps://www.biosino.org/node/project/detail/OEP005446LIVEHTTP 200Resolves, but the content could not be matched to the paper.
- dataSRALIVEHTTP 200https://www.ncbi.nlm.nih.gov/sra/?term=PRJNA1227979Resolves to SRA (data repository).
- datahttps://www.chictr.org.cn/showprojEN.html?proj=180987LIVEHTTP 200Resolves, but the content could not be matched to the paper.
- codeGitHubLIVEHTTP 200https://github.com/LittleQBerry/REVERIE-SportsResolves to GitHub (code repository).
Copyediting
5 minorWording, consistency and formatting errors that need correcting before submission.
No major wording or formatting errors. 5 minor suggestions below.
5 copyedit issues flagged: mostly consistency, clarity, typo.
- MINORtypoAbstract“REVERIE sports intervention was effective in reducing primary outcome fat mass”→ Consider rephrasing to 'REVERIE sports intervention was effective in reducing the primary outcome of fat mass'Missing article 'the' before 'primary outcome'.
- MINORconsistencyData availability section“OEP005446 (10.1109/TSMCB.2011.2170565)”→ The DOI appears incorrect; should be the accession URL or a proper DOI.The DOI is unrelated to the data repository.
- MINORclarityMethods, Statistical analysis“With the exception of the primary outcome measure, whose significance was ascertained by using a two-tailed P < 0.025, all remaining statistical tests were executed with a two-tailed significance level fixed at P < 0.05”→ Clarify the alpha level for the primary outcome; it is unusual to use 0.025.The primary outcome alpha is set at 0.025, which is not standard; consider explaining.
- MINORconsistencyTable 1 footnote“a The modified intention-to-treat population included all participants who had at least one baseline observation.”→ Consider rephrasing to 'The modified intention-to-treat population included all participants with at least one post-baseline observation.'Standard mITT definition includes at least one post-baseline measurement.
- MINORclarityAbstract“REVERIE sports demonstrated superior cognitive enhancements compared to physical sports in exploratory analyses”→ Consider adding 'exploratory' to the claim to avoid overstatement.The paper correctly labels this as exploratory, but the abstract could be clearer.
The published work is robust overall, but an informed reader should weigh the missing explicit ethics approval statement and the minor reporting gaps (randomization method, blinding, outlier handling) as limitations. The absence of an explicit IRB statement is a reporting gap that could warrant a correction or clarification from the authors, though it does not invalidate the study given the trial registration.
- 1.HIGHethicsAdd an explicit ethics approval statement in the Methods section, including the name of the IRB/ethics committee and the approval number, and describe informed consent procedures for participants and guardians.The absence of an explicit ethics statement is a reporting gap that journals and readers expect; it is a fixable issue that should be addressed in a correction or clarification.
- 2.HIGHreportingDescribe the randomization method (e.g., computer-generated random sequence, allocation concealment) in the Methods section.The current text only states that participants were allocated, without specifying the method, which is a key CONSORT item.
- 3.HIGHreportingState whether outcome assessors or data analysts were blinded to group allocation, or provide a rationale for lack of blinding.Blinding is not mentioned; for a behavioral intervention, participant blinding is infeasible, but assessor blinding should be clarified.
- 4.HIGHstatisticsReport the a priori sample size calculation with effect size, alpha, and power in the Methods, or explicitly reference the protocol section where it is detailed.The power analysis is only referenced via the protocol; including it in the main text improves transparency.
- 5.HIGHstatisticsExplicitly state how outliers were handled in the statistical analysis.Outlier handling is not reported, which is a common reviewer request and affects reproducibility.
- 6.HIGHstatisticsProvide exact p-values for all comparisons instead of threshold values like '<0.001' where possible.Exact p-values allow readers to assess the strength of evidence more precisely.
- 7.HIGHstatisticsAdd a statement on verification of statistical test assumptions (normality, homogeneity of variance) in the Methods.Assumption checks are not reported; stating them (or noting robustness) strengthens the statistical analysis.
- 8.HIGHreportingAdd a statement on regulatory compliance (e.g., Declaration of Helsinki) in the Methods or Ethics section.Regulatory compliance is not explicitly stated, which is part of standard ethics reporting.
- 9.HIGHotherVerify the reference 'Rtmdet: an empirical study of designing real-time object detectors' (DOI 10.1016/s2213-8587(22) — appears truncated) as it was not found in the registry; correct the DOI or remove the reference if it cannot be verified.A reference that cannot be found in any registry may be fabricated or contain a DOI error; this is a potential integrity issue.
- 10.MEDIUMreportingClarify the discrepancy between 240 enrolled and 227 analyzed participants in the abstract by referencing the CONSORT diagram or providing the exact number excluded.The internal contradiction flagged by the integrity check could confuse readers; a clear explanation is needed.
- 11.MEDIUMcopyeditFix the DOI in the Data availability section: 'OEP005446 (10.1109/TSMCB.2011.2170565)' appears to be an unrelated DOI; replace it with the correct accession URL or a proper DOI.An incorrect DOI undermines the data availability statement and could mislead readers.
- 12.MEDIUMcopyeditClarify the alpha level for the primary outcome in the Methods: the use of a two-tailed P < 0.025 is unusual and should be explained or justified.The copyedit flagged this as unclear; readers may question the statistical threshold.
- 13.MEDIUMcopyeditRephrase the mITT definition in Table 1 footnote to 'The modified intention-to-treat population included all participants with at least one post-baseline observation.'The current wording 'at least one baseline observation' is non-standard and may be a typo.
- 14.MEDIUMcopyeditIn the Abstract, add 'exploratory' to the claim about cognitive enhancements to avoid overstatement, e.g., 'REVERIE sports demonstrated superior cognitive enhancements compared to physical sports in exploratory analyses'.The paper correctly labels these as exploratory, but the abstract could be clearer to prevent misinterpretation.
- 15.MEDIUMcopyeditFix the missing article in the Abstract: 'REVERIE sports intervention was effective in reducing the primary outcome of fat mass'.Minor grammatical issue that affects readability.
The star rating is the report’s one-glance summary. Every paper starts at 5★ and loses stars for the concrete problems the review finds — so a rating is never a vague average, it’s a running total you can read line by line under “How this rating was calculated.”
- Reporting — 8 dimensionseach dimension that fully fails−½★
- each dimension partially met−¼★
- Statistics · Integrity · Claimseach serious problem−1★
- each medium problem−½★
- Citationseach retracted or unverifiable reference−¼★
- Copyeditonly when the manuscript needs a full edit−½★
The rating never drops below 1★, and a demonstrable critical failure (an impossible statistic, a proven ethics violation) caps it at 1★ on its own — so the stars can never look healthy when the verdict is CRITICAL.
The rating draws on a panel of agents. Three independent Kaimen Rigor reviewers grade the eight dimensions below across several independent passes (the shown verdict is their majority vote — steadier than any single run), isolate the paper’s major claims and check its own evidence backs them, and flag integrity concerns. Alongside them, a citation agent resolves every reference against Crossref, OpenAlex, and Retraction Watch; a statistics agent recomputes reported tests; and rule-based checks verify that declared data/code links actually resolve. Full text is required — an abstract-only submission is not analyzed.
Graded against NIH, MDAR, ARRIVE 2.0, CONSORT, EQUATOR, and RRID guidelines. A dimension that doesn’t apply to the study type is skipped, never penalized.
This Kaimen Rigor review is model-assisted and is not a substitute for formal expert review. It complements human evaluation by surfacing potential methodological concerns — verify each finding against the source.