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Comparison of weight captured via electronic health record and cellular scales to the gold-standard clinical method. | LitMetric

AI Article Synopsis

  • - The study investigates whether body weights collected through cellular scales and electronic health records (EHR) correlate with traditional in-person measurements in weight loss trials.
  • - Comparison of weight data from two different weight loss studies (Log2Lose and MAINTAIN) shows slight variances between remote measurements and in-person weights, but both methods provide consistent direction and magnitude of weight change.
  • - The findings suggest that using cellular scales and EHRs is a viable, cost-effective alternative to in-person measurements for evaluating weight changes in trials, despite minor differences.

Article Abstract

Introduction: Obtaining body weights remotely could improve feasibility of pragmatic trials. This investigation examined whether weights collected via cellular scale or electronic health record (EHR) correspond to gold standard in-person study weights.

Methods: The agreement of paired weight measurements from cellular scales were compared to study scales from a weight loss intervention and EHR-collected weights were compared to study scales from a weight loss maintenance intervention. Differential weight change estimates between intervention and control groups using both pragmatic methods were compared to study collected weight. In the Log2Lose feasibility weight loss trial, in-person weights were collected bi-weekly and compared to weights collected via cellular scales throughout the study period. In the MAINTAIN weight loss maintenance trial, in-person weights were collected at baseline, 14, 26, 42 and 56 weeks. All available weights from the EHR during the study period were obtained.

Results: On average, in Log2Lose cellular scale weights were 0.6 kg (95% CI: -2.9, 2.2) lower than in-person weights; in MAINTAIN, EHR weights were 2.8 kg (SE: -0.5, 6.0) higher than in-person weights. Estimated weight change using pragmatic methods and study scales in both studies were in the same direction and of similar magnitude.

Conclusion: Both methods can be used as cost-effective and real-world surrogates within a tolerable variability for the gold-standard.

Trial Registration: NCT02691260; NCT01357551.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10399518PMC
http://dx.doi.org/10.1002/osp4.656DOI Listing

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