| 1 |
Partly verified |
Full text not readStored summary read |
N01 · Evidence conditionWhich same-day iAUC claim is being checked?Required |
The existing subclaim is lower same-day postprandial iAUC in selected overweight women, originally graded C, with a glucose −34%/insulin −20% note. Subclaim score and safety status are unrecorded and remain distinct from the broader parent C54 question. |
The selected claim, parent material and reports are distinguished and transferred from the stored summary. Detailed original material is unverified and review of existing content remains incomplete. This does not establish completed clinical review or certification. |
Same-day postprandial iAUC in selected overweight women |
Material needed: Original materials identifying the selected population, static standing, comparator, endpoint/time and claim boundaries. The parent score is not used to fill the absent subclaim score. This records needed materials; no new research was executed. |
| 2 |
Partly verified |
Full text not readStored summary read |
N02 · Evidence conditionWho comprised the positive sample?Required |
The positive Henson sample comprised 22 overweight or obese postmenopausal women with dysglycemia. This does not establish the same effect in everyone with established diabetes or in all overweight adults. |
The selected claim, parent material and reports are distinguished and transferred from the stored summary. Detailed original material is unverified and review of existing content remains incomplete. This does not establish completed clinical review or certification. |
Overweight or obese postmenopausal women with dysglycemia |
Material needed: Original eligibility, menopause/glycemia criteria, baseline glucose, medications, comorbidities, ability-to-stand criteria and subgroup denominators. This records needed materials; no new research was executed. |
| 3 |
Partly verified |
Full text not readStored summary read |
N03 · Evidence conditionWhat was the first-day glucose iAUC result?Required |
The original values were 5.3±0.8 with uninterrupted sitting versus 3.5±0.8 mmol/L·h with standing, P=.022, with a −34% record. These are not converted into a single-time-point glucose concentration or used to calculate a new absolute between-condition difference or CI. |
The selected claim, parent material and reports are distinguished and transferred from the stored summary. Detailed original material is unverified and review of existing content remains incomplete. This does not establish completed clinical review or certification. |
Henson first-day glucose iAUC and direct comparison |
Material needed: iAUC baseline/integration interval, model, condition-specific analysis denominators, direct between-condition estimate/CI and the meaning of ±. This records needed materials; no new research was executed. |
| 4 |
Partly verified |
Full text not readStored summary read |
N04 · Evidence conditionIs first-day insulin iAUC a separate endpoint?Required |
The original values were 548.2±71.8 versus 437.2±73.5 mU/L·h, P=.045, with a −20% record. These differ from glucose iAUC values/P and are not transferred into insulin concentrations or complication effects. |
The selected claim, parent material and reports are distinguished and transferred from the stored summary. Detailed original material is unverified and review of existing content remains incomplete. This does not establish completed clinical review or certification. |
Henson first-day insulin iAUC |
Material needed: Insulin iAUC definition, original curves, model, denominators, direct CI, meaning of ±, endpoint hierarchy and relationship to glucose. This records needed materials; no new research was executed. |
| 5 |
Partly verified |
Full text not readStored summary read |
N05 · Evidence conditionWere next-day findings the same?Required |
The original account records a null next-day insulin difference. First-day positive glucose/insulin findings are not copied into the next day; the exact next-day glucose result, values and P are unverified. |
The selected claim, parent material and reports are distinguished and transferred from the stored summary. Detailed original material is unverified and review of existing content remains incomplete. This does not establish completed clinical review or certification. |
First-day positive findings versus null next-day insulin |
Material needed: Next-day conditions, denominators, effects, CIs, P values and original tables for each endpoint. Null findings do not establish zero difference or absence of long-term effects. This records needed materials; no new research was executed. |
| 6 |
Partly verified |
Full text not readStored summary read |
N06 · Evidence conditionWhat did the related older-adult trial find for standing alone?Required |
The Yates acute crossover trial records 60 analyzed and null standing-versus-uninterrupted-sitting findings for primary insulin and glucose. Exact effects, CIs, P values and condition-specific analysis denominators are unverified. |
The selected claim, parent material and reports are distinguished and transferred from the stored summary. Detailed original material is unverified and review of existing content remains incomplete. This does not establish completed clinical review or certification. |
Primary insulin and glucose in the 60 analyzed by Yates |
Material needed: Original result tables, primary-endpoint hierarchy, population/condition denominators, effects, CIs, P values and missing data. Null findings do not prove zero effect or equivalence. This records needed materials; no new research was executed. |
| 7 |
Partly verified |
Full text not readStored summary read |
N07 · Evidence conditionHow are standing and walking separated?Required |
The original account describes walking as more consistently favorable. A nonsignificant walking-versus-standing contrast does not prove equivalence, and walking effects are not transferred to standing. |
The selected claim, parent material and reports are distinguished and transferred from the stored summary. Detailed original material is unverified and review of existing content remains incomplete. This does not establish completed clinical review or certification. |
Activity type, direct comparisons and equivalence boundaries |
Material needed: Activity-specific direct comparisons, effects/CIs, prespecified equivalence criteria, denominators and actual activity records. No new activity instructions are written. This records needed materials; no new research was executed. |
| 8 |
Partly verified |
Full text not readStored summary read |
N08 · Evidence conditionWhat was the original static-standing exposure?Required |
The original record describes five minutes of standing every 30 minutes during 7.5 hours and an already recorded total of 60 minutes of motionless standing per day. Only the preserved total is retained; frequency/exposure is not newly calculated and no implementation instructions are created. |
The selected claim, parent material and reports are distinguished and transferred from the stored summary. Detailed original material is unverified and review of existing content remains incomplete. This does not establish completed clinical review or certification. |
Identification of motionless standing, laboratory day and comparator |
Material needed: Actual protocol, movement/standing verification, meals, concurrent activity, adherence and exposure data. Height-adjustable desks and walking are not substituted. This records needed materials; no new research was executed. |
| 9 |
Partly verified |
Full text not readStored summary read |
N09 · Evidence conditionDid all 22 participants complete every condition?Required |
Henson was a randomized acute incomplete-crossover trial in which 22 participants experienced two of uninterrupted sitting, standing and walking. They are not presented as a denominator completing all three conditions. |
The selected claim, parent material and reports are distinguished and transferred from the stored summary. Detailed original material is unverified and review of existing content remains incomplete. This does not establish completed clinical review or certification. |
Incomplete crossover and condition-specific analysis denominators |
Material needed: Condition combinations/order, washout, period effects, valid condition-specific denominators and allocation/analysis flow. Repeated crossover observations are not counted as additional participants. This records needed materials; no new research was executed. |
| 10 |
Partly verified |
Full text not readStored summary read |
N10 · Evidence conditionDo registered AUC and reported iAUC have matching definitions?Required |
The original evidence endpoint is registered primary postprandial glucose AUC, while results and explanations use glucose iAUC. Both wordings are preserved; matching definitions are not established through a new external registry/paper comparison. |
The selected claim, parent material and reports are distinguished and transferred from the stored summary. Detailed original material is unverified and review of existing content remains incomplete. This does not establish completed clinical review or certification. |
AUC/iAUC wording and endpoint definitions |
Material needed: Original registered endpoint, AUC/iAUC definitions, baseline/negative-area handling, SAP and analysis tables. No arbitrary terminology correction or new discrepancy verdict is created. This records needed materials; no new research was executed. |
| 11 |
Partly verified |
Full text not readStored summary read |
N11 · Evidence conditionWere the positive and null populations identical?Required |
The positive population was overweight postmenopausal women with dysglycemia; the related analysis of 60 concerns a different older population. The Yates bibliography records older South Asians and White Europeans. Findings in another population from the same research team are not copied into the selected population. |
The selected claim, parent material and reports are distinguished and transferred from the stored summary. Detailed original material is unverified and review of existing content remains incomplete. This does not establish completed clinical review or certification. |
Selected women versus a different older population |
Material needed: Report-specific eligibility, sex, age, glycemia, ethnic background, baseline values, denominators and prespecified effect-modification analyses. Conflicting directions and parent R0 are retained. This records needed materials; no new research was executed. |
| 12 |
Partly verified |
Full text not readStored summary read |
N12 · Evidence conditionAre registered-primary and retrospective-registration statements distinguished?Required |
Henson is described as a registered-primary positive signal, but the citation note flags retrospective registration. NCT02135172/NCT02453204 are original citation identifiers; registration dates, changes and prospective status are unread in this work. |
The selected claim, parent material and reports are distinguished and transferred from the stored summary. Detailed original material is unverified and review of existing content remains incomplete. This does not establish completed clinical review or certification. |
Registry identifiers, timing, prospective status and endpoint hierarchy |
Material needed: Initial/changed registration dates, protocols, SAPs, actual start/result-report dates and endpoint hierarchy. Registered-primary wording alone does not certify preregistration or plan adherence. This records needed materials; no new research was executed. |
| 13 |
Unverified |
Full text not readStored summary read |
N13 · Evidence conditionAre direct CIs and the meaning of ± available?Required |
First-day condition-specific ± values, P values and relative reductions are recorded for both iAUC endpoints, but direct between-condition 95% CIs, the meaning of ± and exact Yates/next-day effect intervals are unverified. The ± values are not made into CIs. |
The selected claim, parent material and reports are distinguished and transferred from the stored summary. Detailed original material is unverified and review of existing content remains incomplete. This does not establish completed clinical review or certification. |
Effect intervals and variation definitions for each endpoint/time/contrast |
Material needed: Original model, effect estimator, variation definitions, direct CIs and condition-specific measurements/denominators. No new absolute differences, CIs or relative effects are calculated. This records needed materials; no new research was executed. |
| 14 |
Partly verified |
Full text not readStored summary read |
N14 · Evidence conditionWhat is the clinical meaning of same-day iAUC?Required |
The original parent describes a conditional acute surrogate signal. The original 34%/20% or first-day P values are not converted into long-term HbA1c, diabetes complications or treatment effects. |
The selected claim, parent material and reports are distinguished and transferred from the stored summary. Detailed original material is unverified and review of existing content remains incomplete. This does not establish completed clinical review or certification. |
Acute metabolic measures versus long-term clinical importance |
Material needed: Clinical-importance criteria for the selected population and direct long-term endpoints. No hypothetical glucose-change or risk-reduction examples are created. This records needed materials; no new research was executed. |
| 15 |
Partly verified |
Full text not readStored summary read |
N15 · Evidence conditionWere long-term HbA1c or complications measured?Required |
The other existing subclaim, improved long-term HbA1c or diabetes complications, is graded ?, with an original note that the acute trials did not measure these outcomes. Same-day/next-day materials are not extended into long-term improvement. |
The selected claim, parent material and reports are distinguished and transferred from the stored summary. Detailed original material is unverified and review of existing content remains incomplete. This does not establish completed clinical review or certification. |
Boundaries on extending the same-day question |
Material needed: Direct long-term HbA1c/complication definitions, duration, group-specific denominators, effects and CIs. Nonmeasurement does not certify no effect or the absence of all long-term research. This records needed materials; no new research was executed. |
| 16 |
Partly verified |
Full text not readStored summary read |
N16 · Evidence conditionIs this the same as the eight-week adjustable-desk question?Required |
The original account distinguishes the protocol and core endpoint from verdict 2245’s eight-week height-adjustable desk and broad cardiometabolic question. That verdict is not newly read or assigned a newly constructed link here. |
The selected claim, parent material and reports are distinguished and transferred from the stored summary. Detailed original material is unverified and review of existing content remains incomplete. This does not establish completed clinical review or certification. |
Original verdict 2245 reference and protocol/endpoint differences |
Material needed: Materials comparing those questions with the original protocols/endpoints. Desk installation or long-term management is not treated as a same-day static-standing effect. This records needed materials; no new research was executed. |
| 17 |
Partly verified |
Full text not readStored summary read |
N17 · Evidence conditionAre shared reports counted as independent trials?Required |
Parent 2995 and both subclaim sheets share the Henson/Yates report context. Sheets, reports, crossover conditions and measurement days are not counted as new independent trials, and the 22 participants and 60 analyzed are not summed. Unique-trial and participant totals are unverified. |
The selected claim, parent material and reports are distinguished and transferred from the stored summary. Detailed original material is unverified and review of existing content remains incomplete. This does not establish completed clinical review or certification. |
Reports, cohorts, selected questions and repeated measurements |
Material needed: Report/cohort identities, incomplete-crossover conditions, shared researchers and analysis-population relationships. Unique counts and independence remain unverified. This records needed materials; no new research was executed. |
| 18 |
Partly verified |
Full text not readStored summary read |
N18 · Evidence conditionWhich materials were actually read?Required |
The complete parent stored summary was read and transferred. External abstracts, full texts, registration, protocols and SAPs are unread; a URL does not establish successful access or a fulfilled condition. |
The selected claim, parent material and reports are distinguished and transferred from the stored summary. Detailed original material is unverified and review of existing content remains incomplete. This does not establish completed clinical review or certification. |
Stored summaries versus external originals and registration |
Material needed: Actual acquisition/reading records for originals, appendices, plans and registration. No new external retrieval or access attempt was made in this work. This records needed materials; no new research was executed. |
| 19 |
Partly verified |
Full text not readStored summary read |
N19 · Evidence conditionWhere are bibliographic and registration identifiers recorded?Required |
Henson records PMID 26628415, DOI 10.2337/dc15-1240 and NCT02135172; Yates records PMID 30403772, PMCID PMC6909896, DOI 10.1093/gerona/gly252 and NCT02453204. The original evidence objects have no separate nct field. |
The selected claim, parent material and reports are distinguished and transferred from the stored summary. Detailed original material is unverified and review of existing content remains incomplete. This does not establish completed clinical review or certification. |
DOI, PMID, PMCID and NCT in original citations |
Material needed: Original materials linking report and registration contents/timing. No new URLs are inferred from identifiers; original citation locations and wording are preserved. This records needed materials; no new research was executed. |
| 20 |
Partly verified |
Full text not readStored summary read |
N20 · Evidence conditionAre historical bilingual checks distinguished from this work?Required |
Original bilingual claims/notes and the parent’s historical account of checking two original trials, registries and overlap with 2245 are preserved. Citation statements that findings were checked are historical, not completion of new clinical review, registry verification or independent validation here. |
The selected claim, parent material and reports are distinguished and transferred from the stored summary. Detailed original material is unverified and review of existing content remains incomplete. This does not establish completed clinical review or certification. |
Existing bilingual claims/notes and the scope of historical checks |
Material needed: Original-text, translation, correction and claim-boundary review records. Historical checking language is not relabeled as completed current content review. This records needed materials; no new research was executed. |
| 21 |
Partly verified |
Full text not readStored summary read |
N21 · Evidence conditionAre subclaim values separated from parent grade/axes?Required |
Original subclaim grade C and its note are retained; subclaim score, safety and axes remain unrecorded. Parent C54/Unknown and B/S/R0/I2/E+/B2/CX are parent context, not a subclaim score, safety rating or independence certification. |
The selected claim, parent material and reports are distinguished and transferred from the stored summary. Detailed original material is unverified and review of existing content remains incomplete. This does not establish completed clinical review or certification. |
Original subclaim grade, absent values and parent C54 context |
Material needed: Original selected-subclaim/parent values and boundary checks. No new scores, axes, grades or efficacy reassessment are made. This records needed materials; no new research was executed. |
| 22 |
Partly verified |
Full text not readStored summary read |
N22 · Evidence conditionAre evidence date, corrections and production date distinguished?Required |
Original evidence date 2026-09-07, an empty corrections array and an empty deliberation string are preserved. This is not the current production/content-review date; empty records do not certify that no external corrections exist. |
The selected claim, parent material and reports are distinguished and transferred from the stored summary. Detailed original material is unverified and review of existing content remains incomplete. This does not establish completed clinical review or certification. |
Original evidence date and empty correction/deliberation records |
Material needed: Actual corrections, follow-up materials and complete pre-change history. Original dates and empty arrays are not filled arbitrarily. This records needed materials; no new research was executed. |
| 23 |
Partly verified |
Full text not readStored summary read |
N23 · Evidence conditionAre public funding and company involvement distinguished?Required |
Original funding is university/NIHR/NHS for Henson and UK public/university support for Yates. Public funding does not establish that product support, company employee authors or company analysis/reporting involvement are fully verified. |
The selected claim, parent material and reports are distinguished and transferred from the stored summary. Detailed original material is unverified and review of existing content remains incomplete. This does not establish completed clinical review or certification. |
Funding, product support, employee authors and analysis/reporting roles |
Material needed: Original funding/COI, equipment/product support, author affiliations and analysis/publication roles. Parent I2 is not elevated into current independence certification. This records needed materials; no new research was executed. |
| 24 |
Unverified |
Full text not readStored summary read |
N24 · Evidence conditionAre acute-crossover bias details verified?Required |
Randomized acute incomplete-crossover/crossover design labels are preserved. Details of condition order, washout, period effects, allocation concealment, assessors, meal/measurement standardization, missing data and selective reporting are unverified. |
The selected claim, parent material and reports are distinguished and transferred from the stored summary. Detailed original material is unverified and review of existing content remains incomplete. This does not establish completed clinical review or certification. |
Allocation, order, measurement, missing data and selective reporting |
Material needed: Original methods, registration, protocol, SAP, repeated-measures models, valid values/denominators and reporting changes. A design label does not establish official RoB/GRADE assessment or a passed content review. This records needed materials; no new research was executed. |
| 25 |
Partly verified |
Full text not readStored summary read |
N25 · Evidence conditionAre actual standing exposure and concurrent activity known?Required |
The original 7.5 hours, five minutes every 30 minutes and total of 60 minutes of static standing are preserved only for research identification. Condition-specific actual adherence, movement, meals, concurrent activity and valid measurement denominators are unverified. |
The selected claim, parent material and reports are distinguished and transferred from the stored summary. Detailed original material is unverified and review of existing content remains incomplete. This does not establish completed clinical review or certification. |
Original protocol versus actual adherence/activity records |
Material needed: Original exposure, activity, meal, measurement and adherence records. No new frequency/exposure totals or standing/exercise instructions are created. This records needed materials; no new research was executed. |
| 26 |
Unverified |
Full text not readStored summary read |
N26 · Evidence conditionAre unknown safety and harm collection distinguished?Supplementary |
Parent safety status is Unknown. The original safety explanation records that systematic adverse-event rates in the acute metabolic trials were unavailable. No new harm rates, event counts or between-condition CIs were verified here. |
The selected claim, parent material and reports are distinguished and transferred from the stored summary. Detailed original material is unverified and review of existing content remains incomplete. This does not establish completed clinical review or certification. |
Systematic harm collection, exposure, comparator and denominators |
Material needed: Adverse-event definitions, collection methods, group-specific exposure/denominators, withdrawals, severity and harm results. Unknown is not changed to safe or zero events. This records needed materials; no new research was executed. |
| 27 |
Unverified |
Full text not readStored summary read |
N27 · Evidence conditionWhat about selected participants able to stand and long-term harms?Supplementary |
The original account says findings in selected participants able to stand cannot be generalized directly to people with orthostatic intolerance or vascular/musculoskeletal conditions. Rare harms and long-term risks are not established by the acute summary. |
The selected claim, parent material and reports are distinguished and transferred from the stored summary. Detailed original material is unverified and review of existing content remains incomplete. This does not establish completed clinical review or certification. |
Orthostatic, vascular/musculoskeletal conditions and long-term boundaries |
Material needed: Selection/exclusion criteria, comorbidities, harm surveillance, long-term exposure/denominators and actual follow-up. No new standing, exercise or treatment methods are written. This records needed materials; no new research was executed. |
| 28 |
Partly verified |
Full text not readStored summary read |
N28 · Evidence conditionWhich materials would trigger an update?Required |
This sheet transfers existing same-day iAUC content. Related observations can be updated when selected-subclaim/parent boundaries and original endpoint, timing, comparator, condition-specific denominator, registration, funding, shared-report and harm materials are verified. |
The selected claim, parent material and reports are distinguished and transferred from the stored summary. Detailed original material is unverified and review of existing content remains incomplete. This does not establish completed clinical review or certification. |
Separating source materials, applied conditions, observations and verdict changes |
Material needed: Complete pre-change preservation, material/condition versions, separate application and review records. No new calculations, grades, independence certification or standing/exercise, medication-change or treatment guidance are created. This records needed materials; no new research was executed. |