| 1 |
Partly verified |
Full text not readStored summary read |
N01 · Evidence conditionSelected mean-weight claim and original gradeRequired |
The selected subclaim is “Mean weight loss at 12 months,” with grade C and a note of a −3.8 kg between-group difference. Subclaim score/status/axes are absent; the parent C56 is not used to fill the subclaim score. |
Only the relevant information in the preserved summary is recorded; detailed originals remain unread and existing content review incomplete. Subclaim score, status and axes are absent. Mean results and reaching the 5% threshold are not combined as one endpoint. Existing content review remains incomplete. |
Distinction between original wording/grade, parent score/axes and responder outcomes |
A proposed follow-up study specifying mean change and responder endpoints separately; no new investigation, calculation or trial was performed. |
| 2 |
Partly verified |
Full text not readStored summary read |
N02 · Evidence conditionPopulation, obesity and comorbiditiesRequired |
The population comprised 351 people aged 21–65 at US community health centers, with obesity and at least one of hypertension, diabetes or hyperlipidemia. Results are not extended to other age or health groups. |
Only the relevant information in the preserved summary is recorded; detailed originals remain unread and existing content review incomplete. Obesity/condition definitions, detailed recruitment/exclusions, baseline weight, distribution of conditions and baseline balance remain unverified. Existing content review remains incomplete. |
Actual eligibility, recruitment, baseline weight/conditions and applicable population |
Proposed follow-up comparative research specifying population conditions; no new investigation, calculation or trial was performed in this production. |
| 3 |
Partly verified |
Full text not readStored summary read |
N03 · Evidence conditionAttribution within multicomponent TrackRequired |
The intervention was Track combining an app, a cellular smart scale, 18 dietitian calls and clinician counseling. Which component produced the mean effect cannot be separated. |
Only the relevant information in the preserved summary is recorded; detailed originals remain unread and existing content review incomplete. Independent component effects, designs separating components and their relative contributions remain unverified. Existing content review remains incomplete. |
Distinction between the bundled program and effects of individual components |
A proposed follow-up comparison distinguishing attribution to a bundle, single components and combinations; no new investigation, calculation or trial was performed. |
| 4 |
Partly verified |
Full text not readStored summary read |
N04 · Evidence conditionApp and algorithm rolesRequired |
The original record states that app-based goal self-monitoring and algorithm-tailored feedback were included in the bundle. This is not converted into an effect of a stand-alone app or all digital products. |
Only the relevant information in the preserved summary is recorded; detailed originals remain unread and existing content review incomplete. App version/algorithm, delivery/access, usage, changes and individual effects remain unverified. Existing content review remains incomplete. |
Actual study identity of app-based goal self-monitoring and tailored feedback |
A proposed follow-up study distinguishing the app component from counseling and other elements; no new investigation, calculation or trial was performed. |
| 5 |
Partly verified |
Full text not readStored summary read |
N05 · Evidence conditionSmart-scale self-monitoringRequired |
Daily cellular smart-scale weighing was a self-monitoring element of the research intervention. The primary outcome used separate standardized weight measurement at research visits. No new measurement or management instructions are created. |
Only the relevant information in the preserved summary is recorded; detailed originals remain unread and existing content review incomplete. Device/connectivity, actual use, missing records and correspondence between original data and visit measurements remain unverified. Existing content review remains incomplete. |
Distinction between the connected scale’s intervention role and outcome measurement |
A proposed study reporting intervention self-monitoring separately from endpoint measurement; no new investigation, calculation or trial was performed. |
| 6 |
Partly verified |
Full text not readStored summary read |
N06 · Evidence condition18 dietitian callsRequired |
18 dietitian calls were included in the bundled intervention. The planned number is not converted into actual completion by every participant or an effect of counseling alone. |
Only the relevant information in the preserved summary is recorded; detailed originals remain unread and existing content review incomplete. Delivery/use of each call, counseling intensity, missed calls, providers and other contacts remain unverified. Existing content review remains incomplete. |
Distinction between counseling plans, actual delivery/use and other contacts |
A proposed study distinguishing counseling delivery, actual use and component attribution; no new investigation, calculation or trial was performed. |
| 7 |
Partly verified |
Full text not readStored summary read |
N07 · Evidence conditionClinician counseling and record integrationRequired |
Clinician counseling based on electronic-record recommendations was also included. The original interpretation of technology as an adjunct to counseling is retained; no guidance replacing clinical care or treatment is created. |
Only the relevant information in the preserved summary is recorded; detailed originals remain unread and existing content review incomplete. Actual counseling/contact, decisions, concurrent condition/medication management and differences between groups remain unverified. Existing content review remains incomplete. |
Research scope of electronic-record recommendations, clinician counseling and concurrent management |
A proposed study distinguishing attribution to clinical integration and other elements; no new investigation, calculation or trial was performed. |
| 8 |
Partly verified |
Full text not readStored summary read |
N08 · Evidence conditionUsual-care comparison conditionsRequired |
The original allocation of 176 intervention participants versus 175 receiving usual care is preserved. Usual care is not changed into a group with no management or contact. |
Only the relevant information in the preserved summary is recorded; detailed originals remain unread and existing content review incomplete. Usual-care content, additional control-group support/exposure, crossover use and contact differences remain unverified. Existing content review remains incomplete. |
Actual usual-care management/contact and differences between intervention and control |
A proposed follow-up trial clearly disclosing actual comparison conditions; no new investigation, calculation or trial was performed. |
| 9 |
Partly verified |
Full text not readStored summary read |
N09 · Evidence condition12-month time point and actual exposureRequired |
The primary endpoint was weight change at 12 months. Planned intervention components are not equated with actual use, and no effects of continuation or discontinuation beyond 12 months are generated. |
Only the relevant information in the preserved summary is recorded; detailed originals remain unread and existing content review incomplete. Visit windows, actual exposure duration for each component, follow-up beyond 12 months and changes in use remain unverified. Existing content review remains incomplete. |
Distinction between final 12-month analysis and intervention duration/use |
A proposed follow-up study distinguishing the final time point from continuation/discontinuation follow-up; no new investigation, calculation or trial was performed. |
| 10 |
Partly verified |
Full text not readStored summary read |
N10 · Evidence conditionRandom sequence and allocation concealmentRequired |
The manuscript records that a statistician generated the random sequence and concealed it from study staff until assignment. This is a historical procedure narrative in the preserved summary, not current original-source review or certification. |
Only the relevant information in the preserved summary is recorded; detailed originals remain unread and existing content review incomplete. Allocation records, implementation, exceptions and correspondence with the original protocol/registration remain unread. Existing content review remains incomplete. |
Original allocation-procedure narrative and scope of actual source verification |
Proposed follow-up trial disclosing allocation procedures; no new investigation, calculation or trial was performed in this production. |
| 11 |
Partly verified |
Full text not readStored summary read |
N11 · Evidence conditionMasked outcome assessors and unmasked participantsRequired |
The manuscript records that outcome-measurement staff were masked to allocation, while participants could not be masked because of the intervention. The historical B0 narrative is not used as current verification of all masking. |
Only the relevant information in the preserved summary is recorded; detailed originals remain unread and existing content review incomplete. Original data on assessor/analyst roles, maintenance/breaking of masking and expectation effects remain unread. Existing content review remains incomplete. |
Distinction between assessor masking and intervention characteristics |
A proposed study distinguishing assessor masking from participant expectation effects; no new investigation, calculation or trial was performed. |
| 12 |
Partly verified |
Full text not readStored summary read |
N12 · Evidence conditionStandardized measurements and weight-change definitionRequired |
The primary endpoint was standardized measured weight change at research visits at 12 months. App entries, self-reports and daily smart-scale logs are not used as the same endpoint. |
Only the relevant information in the preserved summary is recorded; detailed originals remain unread and existing content review incomplete. Details of baseline/visit measurements, equipment/calibration, conditions, measurement windows and handling of repeats remain unverified. Existing content review remains incomplete. |
Visit measurements, change from baseline, units and measurement windows |
A proposed study reporting measured outcomes separately from remote self-monitoring; no new investigation, calculation or trial was performed. |
| 13 |
Partly verified |
Full text not readStored summary read |
N13 · Evidence conditionGroup-specific mean changes and CIsRequired |
Original values are preserved: intervention −4.0 kg (95% CI −4.9 to −3.0) and usual care −0.1 kg (−1.0 to 0.8). Rounded group values are not newly subtracted or converted into final absolute weights. |
Only the relevant information in the preserved summary is recorded; detailed originals remain unread and existing content review incomplete. Group-specific baseline/final absolute values, model/adjustment details for each estimate and individual distributions remain unverified. Existing content review remains incomplete. |
Separate estimands for changes within each group and the between-group effect |
A proposed study reporting group changes and the between-group estimate distinctly together; no new investigation, calculation or trial was performed. |
| 14 |
Partly verified |
Full text not readStored summary read |
N14 · Evidence conditionBetween-group difference of −3.8 kgRequired |
The between-group difference was −3.8 kg (95% CI −5.0 to −2.5), P<0.001. The original estimate is preserved; no new difference/CI, standardized effect or relative weight-loss rate is calculated. |
Only the relevant information in the preserved summary is recorded; detailed originals remain unread and existing content review incomplete. Exact model terms, adjustment/baseline correspondence and data for reproducing estimates remain unread. Existing content review remains incomplete. |
Exact original 12-month between-group difference, CI and P value |
A proposed follow-up study disclosing the primary effect estimate and uncertainty; no new investigation, calculation or trial was performed. |
| 15 |
Partly verified |
Full text not readStored summary read |
N15 · Evidence conditionMean, individual response and the 5% thresholdRequired |
At least 5% weight loss, 40% versus 17% with P<0.001, was a separate secondary responder result. Threshold attainment or event counts are not calculated from mean values of −4.0/−0.1 or −3.8 kg. |
Only the relevant information in the preserved summary is recorded; detailed originals remain unread and existing content review incomplete. Individual baseline/change distributions, threshold calculation, responder denominators/event counts and CIs remain unverified. Existing content review remains incomplete. |
Distinction between continuous mean change and the secondary responder endpoint |
A proposed follow-up trial distinguishing mean and prespecified responder outcomes; no new investigation, calculation or trial was performed. |
| 16 |
Partly verified |
Full text not readStored summary read |
N16 · Evidence condition351 participants, 176/175 and denominatorsRequired |
351 randomized participants (176/175) are preserved as recorded. Enrollment is not used to imply measurement of every participant at 12 months or the observed denominator for every analysis. |
Only the relevant information in the preserved summary is recorded; detailed originals remain unread and existing content review incomplete. 12-month measurement, model-analysis, group-specific visit/response denominators and analysis-inclusion criteria remain unverified. Existing content review remains incomplete. |
Randomized population and endpoint-specific analysis/measurement denominators |
A proposed follow-up study distinguishing randomized, observed and estimated denominators; no new investigation, calculation or trial was performed. |
| 17 |
Partly verified |
Full text not readStored summary read |
N17 · Evidence conditionITT principle and estimand populationRequired |
The manuscript records following the ITT principle. This historical narrative is not used to establish analysis-population details, completeness of all observations or current content-review verification. |
Only the relevant information in the preserved summary is recorded; detailed originals remain unread and existing content review incomplete. Primary-effect inclusion criteria, estimand-population definitions, analysis exceptions and original PPS/sensitivity results remain unread. Existing content review remains incomplete. |
ITT narrative and outcome-specific analysis conditions |
A proposed study disclosing ITT separately from other analyses; no new investigation, calculation or trial was performed. |
| 18 |
Partly verified |
Full text not readStored summary read |
N18 · Evidence conditionMissing data and maximum-likelihood modelRequired |
The manuscript records that missing observations were estimated by maximum likelihood in the prespecified model. This is not changed into measurement of all participants or absence of missing-data effects. |
Only the relevant information in the preserved summary is recorded; detailed originals remain unread and existing content review incomplete. Group-specific reasons/timing of missingness/attrition, model terms/assumptions, sensitivity to non-random missingness and actual numbers remain unverified. Existing content review remains incomplete. |
Distinction between missing-data narratives, missingness/attrition and model assumptions |
A proposed study distinguishing observations from estimates when reporting missing-data effects; no new investigation, calculation or trial was performed. |
| 19 |
Partly verified |
Full text not readStored summary read |
N19 · Evidence conditionRegistration and prespecified primary endpointRequired |
Original records of NCT01827800, posting on 2013-04-10 and allocation starting on 2013-06-18 are preserved. The narrative that these matched the primary 12-month weight-change endpoint is historical; full registration/plans remain unread in this work. |
Only the relevant information in the preserved summary is recorded; detailed originals remain unread and existing content review incomplete. Registration changes, protocol/SAP, the complete pre-recruitment analysis conditions and original-source correspondence remain unread. Existing content review remains incomplete. |
Preserved scope of the NCT identifier, advance dates and endpoint plan |
A proposed study openly linking advance plans and actual primary analysis; no new investigation, calculation or trial was performed. |
| 20 |
Partly verified |
Full text not readStored summary read |
N20 · Evidence conditionMultiple outcomes, time points and hierarchyRequired |
The manuscript’s primary mean weight endpoint at 12 months is distinguished from the secondary 5% responder result. Reductions in blood pressure, glucose or disease events, or primary effects at other time points, are not generated. |
Only the relevant information in the preserved summary is recorded; detailed originals remain unread and existing content review incomplete. The complete outcomes/time points, multiplicity adjustment, analysis/reporting changes and secondary-result tables remain unverified. Existing content review remains incomplete. |
Advance hierarchy of the primary mean endpoint, responders and other outcomes |
A proposed study distinguishing the primary endpoint from secondary results; no new investigation, calculation or trial was performed. |
| 21 |
Unverified |
Full text not readStored summary read |
N21 · Evidence conditionConcurrent management, medication and lifestyleRequired |
This was a bundled study involving comorbidities and clinician counseling. It does not establish that concurrent management, medication or lifestyle beyond the app, scale and counseling were equal or had no effect. |
Information currently needed is unverified in the preserved summary. Details of concurrent management/medication changes, diet/activity, group-specific exposure and handling of differences remain unverified. Existing content review remains incomplete. |
Group-specific effects of conditions/medication, diet/activity and clinical contact |
A proposed follow-up study distinguishing concurrent management from intervention components; no new investigation, calculation or trial was performed. |
| 22 |
Partly verified |
Full text not readStored summary read |
N22 · Evidence conditionWeight, clinical events and importanceRequired |
The original verdict distinguishes weight from actual events such as disease onset or death. The manuscript’s statement that no prespecified success threshold or externally validated minimum clinically important difference was declared is preserved. |
Only the relevant information in the preserved summary is recorded; detailed originals remain unread and existing content review incomplete. Declared clinical-importance/success criteria, disease events and long-term functional effects remain unverified. Existing content review remains incomplete. |
Distinction between weight change, clinical events and success/importance criteria |
A proposed study distinguishing weight from clinical outcomes important to patients; no new investigation, calculation or trial was performed. |
| 23 |
Partly verified |
Full text not readStored summary read |
N23 · Evidence conditionNIH public fundingRequired |
NIH NIDDK support through R01DK093829 is preserved as recorded. Public funding is not converted into absence of all support/author relationships or new independence certification. |
Only the relevant information in the preserved summary is recorded; detailed originals remain unread and existing content review incomplete. Funder roles, agreements, data/publication decisions and complete original support statements remain unread. Existing content review remains incomplete. |
Distinction between actual funder/grant and other support categories |
A proposed follow-up trial disclosing support roles; no new investigation, calculation or trial was performed. |
| 24 |
Partly verified |
Full text not readStored summary read |
N24 · Evidence conditionCommercial, scale, analysis/writing/publication supportRequired |
The manuscript states that the pivotal paper did not report commercial sponsorship, donated scales, outsourced analysis, medical writing or publication-fee support. Non-reporting is not judged as actual absence. |
Only the relevant information in the preserved summary is recorded; detailed originals remain unread and existing content review incomplete. Each support category, actual agreements, complete originals and research roles remain unread. Existing content review remains incomplete. |
Scope of category-specific non-reporting in the pivotal paper |
A proposed study disclosing support categories separately; no new investigation, calculation or trial was performed. |
| 25 |
Partly verified |
Full text not readStored summary read |
N25 · Evidence conditionLater author relationships and historical attributionRequired |
The manuscript records a later paper disclosing Gary Bennett’s WW scientific-adviser role and equity in Coeus Health. A later disclosure after the pivotal trial is not applied retrospectively as confirmation of funding or roles during that trial. |
Only the relevant information in the preserved summary is recorded; detailed originals remain unread and existing content review incomplete. Specific later bibliography/disclosure dates, contemporaneous agreements, relationships during the original trial and complete COI remain unlinked/unread. Existing content review remains incomplete. |
Timing, individuals and relation of later disclosures to the original trial |
A proposed study reporting support and author relationships separately by period; no new investigation, calculation or trial was performed. |
| 26 |
Partly verified |
Full text not readStored summary read |
N26 · Evidence conditionOther low-intensity null trials and applicability differencesRequired |
Null trials of app-only or low-intensity technology support are mentioned, but the original explanation treats them as generalization limits rather than direct refutations of Track because composition and intensity differ. Unlinked reports are not created as new trials. |
Only the relevant information in the preserved summary is recorded; detailed originals remain unread and existing content review incomplete. Specific bibliography, population/intervention/denominators, endpoints and results of the other trials are not linked. Existing content review remains incomplete. |
Distinction between references to null programs and direct Track comparisons |
A proposed follow-up study matching composition and intensity for comparison; no new investigation, calculation or trial was performed. |
| 27 |
Partly verified |
Full text not readStored summary read |
N27 · Evidence conditionSame report, sibling sheets and independent replicationRequired |
The mean and 5% sheets share the same Bennett2018 Track report of 351 randomized participants. Groups, time points, app/counseling components, bibliography/registration and sibling sheets are not added as new independent trials or participants. |
Only the relevant information in the preserved summary is recorded; detailed originals remain unread and existing content review incomplete. Independent reproduction with the same composition/endpoint and unique trial/participant totals are not established. Existing content review remains incomplete. |
Report-to-trial-to-group/time-point/denominator relationships |
A proposed independent follow-up comparison of the same bundle/endpoint; no new investigation, calculation or trial was performed. |
| 28 |
Partly verified |
Full text not readStored summary read |
N28 · Evidence conditionPersistence and generalization across products/populationsRequired |
Results are limited to the population and duration of the Track bundle including counseling. They are not extended to all apps/commercial products, other populations, persistence beyond 12 months or disease-treatment effects. |
Only the relevant information in the preserved summary is recorded; detailed originals remain unread and existing content review incomplete. Long-term/discontinuation follow-up, other populations/compositions and direct single-component comparisons remain unverified. Existing content review remains incomplete. |
12-month bundle results versus later effects or other programs |
A proposed follow-up study distinguishing applicability by bundle, population and duration; no new investigation, calculation or trial was performed. |
| 29 |
Partly verified |
Full text not readStored summary read |
N29 · Harm-information gaps supplementing the efficacy tableOriginal safety record and reporting gapsSupplementary |
Parent safety is unknown, and the manuscript states that the pivotal paper did not systematically present adverse events as a prespecified safety endpoint. Mean weight loss is not used as absence of harm or safety of disease management. |
Only the relevant information in the preserved summary is recorded; detailed originals remain unread and existing content review incomplete. Adverse-event collection/adjudication, group-specific frequencies/denominators, discontinuation and long-term/vulnerable-population harms remain unverified. Existing content review remains incomplete. |
Prespecification, collection and group-specific denominators/follow-up for adverse events |
A proposed study specifying harm collection and population-specific follow-up; no new investigation, calculation or trial was performed. |
| 30 |
Partly verified |
Full text not readStored summary read |
N30 · Evidence conditionParent/subclaim, Korean/English, dates and historyRequired |
Parent C56, B/S/R1/I2/E+/B0, unrecorded precision, three false flags, empty override reasons and subclaim grade C/note are preserved. Korean/English text, 2026-08-26, empty corrections/deliberation and historical cross-checking are not current review or a subclaim score. |
Only relevant preserved-summary information is recorded; detailed originals remain unread and existing content review incomplete. Missing subclaim score/status/axes are not filled with parent values. No new efficacy/method certification. Existing content review remains incomplete. |
Separation of original values/axes from corrections and historical verification narratives |
A proposed study distinguishing original values/history from the applicability of later updates; no new investigation, calculation or trial was performed. |
| 31 |
Partly verified |
Full text not readStored summary read |
N31 · Evidence conditionActual summary reading and external linksRequired |
The full preserved JSON summary and bibliography were used for production, and links are retained. Papers, registration, protocol, SAP and original later disclosures/support materials remain unread with no access attempt; links were not tested. |
Only the relevant information in the preserved summary is recorded; detailed originals remain unread and existing content review incomplete. External-source contents, exact denominators/models and actual accessibility remain unverified. Existing content review remains incomplete. |
Reading the preserved JSON versus access to external originals, registration, plans and COI |
A proposed follow-up study updating acquisition, timing and scope separately; no new investigation, calculation or trial was performed. |