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Incentives and Reminders to Improve Long-term Medication Adherence (INMIND): Protocol for a Pilot Randomized Controlled Trial.
Stecher, Chad; Ghai, Ishita; Lunkuse, Lillian; Wabukala, Peter; Odiit, Mary; Nakanwagi, Agnes; Linnemayr, Sebastian.
Afiliação
  • Stecher C; College of Health Solutions, Arizona State University, Phoenix, AZ, United States.
  • Ghai I; Pardee RAND Graduate School, Santa Monica, CA, United States.
  • Lunkuse L; Mildmay Uganda, Kampala, Uganda.
  • Wabukala P; Mildmay Uganda, Kampala, Uganda.
  • Odiit M; Mildmay Uganda, Kampala, Uganda.
  • Nakanwagi A; Mildmay Uganda, Kampala, Uganda.
  • Linnemayr S; RAND Corporation, Santa Monica, CA, United States.
JMIR Res Protoc ; 11(10): e42216, 2022 Oct 31.
Article em En | MEDLINE | ID: mdl-36315224
ABSTRACT

BACKGROUND:

Nonadherence to antiretroviral therapy (ART) among people living with HIV is a crucial barrier to attaining viral suppression globally. Existing behavioral interventions have successfully increased ART adherence, but typically show only short-term impact that dissipates after the interventions are withdrawn.

OBJECTIVE:

This study aims to test the feasibility, acceptability, and preliminary efficacy of a novel intervention that uses SMS text messages and conditional incentives to support ART initiators in establishing pill-taking habits.

METHODS:

A sample of 150 participants aged ≥18 years who have initiated ART in the preceding 3 months will be recruited from Mildmay Uganda in Kampala, Uganda. All (150/150, 100%) participants will be educated on the anchoring strategy and will choose an existing routine to pair with their daily ART adherence from a set of 3 suggested routines getting dressed in the morning, eating breakfast, or eating dinner. Then, participants will be randomized to receive either usual care (control group 50/150, 33.3%) or 1 of the 2 interventions delivered over 3 months daily SMS text message reminders to follow their chosen anchoring plan (messages group; treatment group 1 50/150, 33.3%) or daily SMS text messages and incentives conditional on taking their ART medication around the time of their chosen anchor (incentives group; treatment group 2 50/150, 33.3%). Long-term ART adherence will be evaluated for 6 months after the intervention, and survey assessments will be conducted at baseline, 3 months, and 9 months. Outcomes include feasibility and acceptability measures and intervention efficacy outcomes defined by electronically measured mean medication adherence during the intervention and during the 6 months after the intervention, along with a measure of routine ART adherence based on taking medications around the time of participants' anchor during the intervention and during the 6 months after intervention.

RESULTS:

As of February 18, 2022, recruitment was completed. A total of 150 participants were recruited, and data collection is expected to end in December of 2022. Final results are expected to be submitted for publication by April 2023.

CONCLUSIONS:

This study is the first to use behavioral economics-based interventions in combination with the anchoring strategy to improve long-term ART adherence among treatment initiators. We hypothesize that the combination of SMS text message reminders and incentives will increase participants' use of their anchoring strategy, and thus medication adherence will be better maintained after the intervention ends in our intervention groups relative to the control group that uses only the anchoring strategy. Results of this pilot study will help to refine this combined intervention approach for testing at scale and broaden our understanding of the habit formation process. TRIAL REGISTRATION ClinicalTrials.gov NCT05131165; https//clinicaltrials.gov/ct2/show/NCT05131165. INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID) DERR1-10.2196/42216.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials Idioma: En Ano de publicação: 2022 Tipo de documento: Article