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Can a participant-referred ‘study buddy’ increase retention of rural people who use drugs in research? A multi-site, randomized trial

  • April M. Young
  • , Kathryn E. Lancaster
  • , Miriam R. Elman
  • , Sarann Bielavitz
  • , Ryan R. Cook
  • , Angela T. Estadt
  • , Madison N. Enderle
  • , Edward Freeman
  • , Jodi Lapidus
  • , Philip T. Korthuis

Producción científica: Articlerevisión exhaustiva

1 Cita (Scopus)

Resumen

Aims: To test the efficacy of a participant-referred “study buddy” intervention compared with standard retention strategies in retaining rural people who use drugs (PWUD) in longitudinal research. Design: Multi-site, two-arm, randomized controlled trial. Setting: Rural counties in Ohio, Oregon, and Kentucky, USA. Participants: People enrolled in the Peer-based Retention Of people who Use Drugs in Rural Research (PROUD-R2) study who were 18 years or older, resided in the study area, and used opioids or injected any drug to get high in the past 30 days between August 2020 and August 2022. Participants (n = 739) were 42% female, mostly White (89%) and non-Hispanic (96%), unstably housed (57%), and reported lifetime injection drug use (93%). The most common drugs of choice were methamphetamine (42%) and heroin (38%). Intervention and Comparator: Participants were allocated (1:1, stratified by site), to: [1] standard retention approach involving appointment reminders and contact information updates by study staff (n = 365), or [2] the intervention arm, receiving the standard retention approach and asked to recruit a “study buddy” (n = 374). Study buddies were invited to view a training video and instructed to encourage their intervention participant to attend follow-up appointments. Measurements: Intervention, control, and study buddy participants completed interviewer-administered surveys at baseline and at 6 and 12 months. Outcomes included retention at 12 months (primary) and 6 months (secondary). Findings: Retention was 50.3% at 6 months and 46.1% at 12 months. Only 23.5% of intervention participants recruited a study buddy. In intent-to-treat analyses, the intervention did not increase retention at 12 (adjusted odds ratio [AOR] 1.08, 95% confidence interval [CI] 0.79–1.47) or 6 (AOR 0.96, 95% CI 0.69–1.34) months. Conclusions: Recruitment of self-identified “study buddies” did not appear to statistically significantly improve retention of rural people who use drugs in this longitudinal study at 6- and 12-month follow-up relative to standard retention approaches.

Idioma originalEnglish
Páginas (desde-hasta)894-907
Número de páginas14
PublicaciónAddiction
Volumen121
N.º4
DOI
EstadoPublished - abr 2026

Nota bibliográfica

Publisher Copyright:
© 2025 Society for the Study of Addiction.

Financiación

PROUD‐R is funded by the National Institutes of Health (NIH) through National Center for Advancing Translational Sciences U01TR002631 (MPIs: P.T.K. and A.M.Y.). The Rural Opioid Initiative studies that are integrated with PROUD‐R are funded by the National Institute on Drug Abuse through grants UG3/UH3 DA044798 (PIs: A.M.Y. and Cooper), UH3DA044831 (PI: P.T.K), UH3DA044822 (PIs: Miller and Go). K.E.L. was supported by K01DA048174 (PI: K.E.L.). R.R.C. was supported by K01DA55130 (PI: R.R.C.). A.T.E. was supported by F31DA054752 (PI: A.T.E.). The project is also supported by UL1TR002369 (Oregon Clinical & Translational Research Institute), UL1TR001998 (University of Kentucky Center for Clinical and Translational Science) and UL1TR001070 (The Ohio State University Center for Clinical and Translational Science) from the NIH, and K12 HS026370 from Patient‐Centered Outcomes Research Institute. The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH. The study sponsor had no role in the study design, the collection, management and interpretation of data, the writing of this article or the decision to submit this article for publication. This study protocol was approved by the University of Utah Institutional Review Board, the multi‐site study single Institutional Review Board. Funding information

FinanciadoresNúmero del financiador
National Institutes of Health (NIH)
University of Kentucky, Center for Clinical and Translational ScienceUL1TR001070
Oregon Clinical and Translational Research InstituteUL1TR001998
National Institute on Drug AbuseK01DA048174, UL1TR002369, F31DA054752, UG3/UH3 DA044798, UH3DA044822, K01DA55130, UH3DA044831
Ohio Water Resources Center, Ohio State UniversityK12 HS026370
National Center for Advancing Translational Sciences (NCATS)U01TR002631

    ODS de las Naciones Unidas

    Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible

    1. Good health and well being
      Good health and well being

    ASJC Scopus subject areas

    • Medicine (miscellaneous)
    • Psychiatry and Mental health

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