Reinforcement Learning in Diabetes Mellitus Trial (REINFORCE)
Primary Purpose
Diabetes Mellitus, Type 2, Medication Adherence
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Reinforcement Learning
Sponsored by

About this trial
This is an interventional health services research trial for Diabetes Mellitus, Type 2
Eligibility Criteria
Inclusion criteria:
- Age between 18-84 years
- Diagnosed with type 2 diabetes mellitus (T2DM) and are prescribed between 1-3 daily oral medications for this disease
- Currently have a smartphone with a data plan or WiFi at home
- HbA1c level ≥7.5%
- Basic working knowledge of English
- Willing and able to set up the platform and adhere to study procedures
- Either not currently using a pillbox or willing to use electronic pill bottles (EDMs) for diabetes medications for the duration of the study
Exclusion criteria:
- Patients with active enrollment in another diabetes trial within Mass General Brigham
- Patients who receive daily assistance with taking their medications at home
- Patients who are unable to receive text messages for more than 3 days in a row during the study period
Sites / Locations
- Brigham and Women's Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Reinforcement Learning Intervention Arm
Control Arm
Arm Description
Up to daily, tailored text messages.
Up to daily, untailored text messages.
Outcomes
Primary Outcome Measures
Medication Adherence
Medication adherence to type 2 diabetes oral medications (averaged) as measured by the number of dates and times of pillbottle openings in the electronic pill bottles
Secondary Outcome Measures
Glycemic Control
Change in glycated hemoglobin A1c from baseline to end of the 6-month follow-up
Full Information
NCT ID
NCT04473326
First Posted
July 13, 2020
Last Updated
February 6, 2023
Sponsor
Brigham and Women's Hospital
Collaborators
National Institute on Aging (NIA)
1. Study Identification
Unique Protocol Identification Number
NCT04473326
Brief Title
Reinforcement Learning in Diabetes Mellitus Trial
Acronym
REINFORCE
Official Title
Optimizing Message Framing for Healthy Habits for Patients With Type 2 Diabetes - Phase II (Pragmatic Trial)
Study Type
Interventional
2. Study Status
Record Verification Date
February 2023
Overall Recruitment Status
Completed
Study Start Date
February 4, 2021 (Actual)
Primary Completion Date
January 4, 2022 (Actual)
Study Completion Date
January 28, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Brigham and Women's Hospital
Collaborators
National Institute on Aging (NIA)
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
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 this pilot study is to develop and test a novel reinforcement learning-enhanced text messaging program to support medication adherence in patients with type 2 diabetes. Type 2 diabetes is an optimal condition in which to test 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 pilot study will be a parallel randomized pragmatic trial comparing medication adherence and clinical outcomes for adults 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. Our outcomes of interest will be medication adherence, as measured by electronic pill bottles, and HbA1c levels.
Detailed Description
The goal of this pilot study is to develop and test a novel reinforcement learning-enhanced text messaging program to support medication adherence in patients with type 2 diabetes. This pilot study will be a parallel randomized pragmatic trial comparing medication adherence and clinical outcomes for adults 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, untailored text messages. Our outcomes of interest will be medication adherence, as measured by electronic pill bottles, and HbA1c levels.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Type 2, Medication Adherence
7. Study Design
Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
60 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Reinforcement Learning Intervention Arm
Arm Type
Experimental
Arm Description
Up to daily, tailored text messages.
Arm Title
Control Arm
Arm Type
No Intervention
Arm Description
Up to daily, untailored text messages.
Intervention Type
Behavioral
Intervention Name(s)
Reinforcement Learning
Intervention Description
Participants in the intervention arm will receive up to daily, tailored text messages based on their electronic pill bottle-measured adherence. Given the participants' baseline characteristics and time-varying responses to the messages, a reinforcement learning algorithm will deliver different text messages and adapt over time to determine which type of messaging works best for each individual participant.
Primary Outcome Measure Information:
Title
Medication Adherence
Description
Medication adherence to type 2 diabetes oral medications (averaged) as measured by the number of dates and times of pillbottle openings in the electronic pill bottles
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Glycemic Control
Description
Change in glycated hemoglobin A1c from baseline to end of the 6-month follow-up
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
84 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria:
Age between 18-84 years
Diagnosed with type 2 diabetes mellitus (T2DM) and are prescribed between 1-3 daily oral medications for this disease
Currently have a smartphone with a data plan or WiFi at home
HbA1c level ≥7.5%
Basic working knowledge of English
Willing and able to set up the platform and adhere to study procedures
Either not currently using a pillbox or willing to use electronic pill bottles (EDMs) for diabetes medications for the duration of the study
Exclusion criteria:
Patients with active enrollment in another diabetes trial within Mass General Brigham
Patients who receive daily assistance with taking their medications at home
Patients who are unable to receive text messages for more than 3 days in a row during the study period
Facility Information:
Facility Name
Brigham and Women's Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02120
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
34862289
Citation
Lauffenburger JC, Yom-Tov E, Keller PA, McDonnell ME, Bessette LG, Fontanet CP, Sears ES, Kim E, Hanken K, Buckley JJ, Barlev RA, Haff N, Choudhry NK. REinforcement learning to improve non-adherence for diabetes treatments by Optimising Response and Customising Engagement (REINFORCE): study protocol of a pragmatic randomised trial. BMJ Open. 2021 Dec 3;11(12):e052091. doi: 10.1136/bmjopen-2021-052091.
Results Reference
derived
Learn more about this trial
Reinforcement Learning in Diabetes Mellitus Trial
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