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Refinement and Adaption of Reinforcement Learning to Personalize Behavioral Messaging for Healthy Habits (REINFORCE2)

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Mass General Brigham

Status

Active, not recruiting

Conditions

Medication Adherence
Diabetes Mellitus, Type 2

Treatments

Behavioral: Reinforcement Learning

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT05742685
P30AG064199-04 (U.S. NIH Grant/Contract)
2023P000293

Details and patient eligibility

About

Reinforcement learning is an advanced analytic method that discovers each individual's pattern of responsiveness by observing their actions and then implements a personalized strategy to optimize individuals' behaviors using trial and error. The goal of the proposed research is to refine, adapt and perform efficacy testing of a novel reinforcement learning-based text messaging intervention to support medication adherence for patients with type 2 diabetes within a community health center setting. This study will be a parallel randomized pragmatic trial comparing medication adherence and clinical outcomes for adults in a community setting aged 18-84 with type 2 diabetes who are prescribed 1-3 daily oral medications for this disease. Participants will be randomized to one of two arms for the duration of the study period: (1) a reinforcement learning intervention arm with up to daily, tailored text messages based on time-varying treatment-response patterns; or (2) a control arm with up to daily, un-tailored text messages. Outcomes of interest will be medication adherence, as measured by electronic pill bottles, and HbA1c levels over 6 months.

Full description

The goal of the proposed research is to refine, adapt and perform efficacy testing of a novel reinforcement learning-based text messaging intervention to support medication adherence for patients with type 2 diabetes within a community setting. Type 2 diabetes is an optimal condition in which to refine this program, as it is one of the most prevalent chronic conditions in the US adult population and requires most patients to be on daily or twice daily doses of medications. This study will be a parallel randomized pragmatic trial comparing medication adherence and clinical outcomes for adults in a community setting aged 18-84 with type 2 diabetes who are prescribed 1-3 daily oral medications for this disease. Participants will be randomized to one of two arms for the duration of the study period: (1) a reinforcement learning intervention arm with up to daily, tailored text messages based on time-varying treatment-response patterns; or (2) a control arm with up to daily, un-tailored text messages. Outcomes of interest will be medication adherence, as measured by electronic pill bottles, and HbA1c levels over 6 months.

Enrollment

28 patients

Sex

All

Ages

18 to 84 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosis of Type 2 Diabetes Mellitus (T2DM)
  • Prescribed between 1-3 daily oral medications for diabetes
  • Most recent HbA1c level of 7% or greater
  • Suboptimal adherence, defined by proportion of days covered (PDC) < 0.90 based on chart review
  • Must have a smartphone for which they are the sole user
  • Must have a basic working knowledge of English or Spanish

Exclusion criteria

  • Currently using a pillbox and/or not willing to use electronic pill bottles for 6 months
  • Receive help at home on a daily basis with taking medications

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

28 participants in 2 patient groups

Reinforcement Learning Intervention Arm
Experimental group
Description:
Up to daily, tailored text messages.
Treatment:
Behavioral: Reinforcement Learning
Control Arm
No Intervention group
Description:
Up to daily, untailored text messages.

Trial contacts and locations

1

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Central trial contact

Julie Lauffenburger, PharmD, PhD

Data sourced from clinicaltrials.gov

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