Three week compared to seven week run-in period length and the assessment of pre-randomization adherence: A study within a trial

On behalf of the ACHIEVE investigators

Résultat de recherche: Articleexamen par les pairs

Résumé

Background/aims: To examine how measuring adherence at 3 weeks by self-report and pill counts compares to measurements at 7 weeks in a pre-randomization run-in period. Methods: Study within a trial of an international parallel group randomized controlled trial (RCT) that compares spironolactone to placebo. Adults receiving dialysis enter an 8-week active run-in period with spironolactone. Adherence was assessed by both self-report and pill counts in a subgroup of participants at both 3 weeks and 7 weeks. Results: 332 participants entered the run-in period of which 166 had complete data. By self-report, 146/166 (94.0%) and 153/166 (92.2%) had at least 80% adherence at 3 and 7 weeks respectively (kappa = 0.27 (95% C.I. 0.16 to 0.38). By pill counts, the mean (SD) adherence was 96.5% (16.1%) and 92.4% (18.2%) at 3 and 7 weeks respectively (r = 0.32) with a mean (SD) difference of 3.1% (17.8%) and a 95% limit of agreement from −31.7% to +37.9%. The proportion of adherent participants by self-report and pill counts at 3 weeks agreed in 87.4% of participants (McNemar's p-value 0.58, kappa 0.11, p = 0.02) and at 7 weeks agreed in 92.2% (McNemar's p-value 0.82, kappa 0.47, p < 0.001). Conclusions: Three and seven-week run-in periods and both self-reported and pill count assessments performed similarly. Trial registration: ClinicalTrials.gov Identifier: NCT03020303

Langue d'origineEnglish
Numéro d'article106466
JournalContemporary Clinical Trials
Volume107
DOI
Statut de publicationPublished - août 2021

Note bibliographique

Publisher Copyright:
© 2021

ASJC Scopus Subject Areas

  • Pharmacology (medical)

PubMed: MeSH publication types

  • Journal Article
  • Randomized Controlled Trial

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