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Medication Adherence Patterns in Rheumatic Diseases: A Behavioral Trial

Primary Purpose

Rheumatic Diseases, Gout, Adherence, Medication

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Cue-Reward Intervention
Cue-Reward Intervention with possible intensification
Sponsored by
Brigham and Women's Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Rheumatic Diseases

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • English-speaking patients
  • receiving their care at a Brigham and Women's Hospital-affiliated rheumatology practice
  • >=18 years of age
  • with rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), or gout
  • prescribed >=1 oral medication for this disease for >=4 months.
  • for patients with gout, had a uric acid level checked in the prior 18 months and the most recent level is >6.
  • for patients with SLE, their most recent c-reactive protein level collected in the past 18 months must be >10.
  • currently have a smartphone with a data plan or WiFi at home
  • 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:

  • Pregnant women
  • Incarcerated individuals

Sites / Locations

  • Brigham and Women's Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

No Intervention

Experimental

Experimental

Arm Label

Control

Cue-Reward Intervention

Cue-Reward Intervention with possible intensification.

Arm Description

Patients in the control arm will not receive any intervention (but will receive electronic pill bottles to monitor their adherence).

Patients in this intervention arm will choose an event-based cue and receive reminder text messages reminding them of their cue. Additionally, a donation will be made to a local charity every time they take their medication.

Patients in this intervention arm will choose an event-based cue. Additionally, a donation will be made to a local charity every time they take their medication. Those who show no improvement in adherence after 6 weeks will start receiving reminder text messages reminding them of their cue.

Outcomes

Primary Outcome Measures

Rate of Medication Adherence
Medication adherence will be measured as the percentage of times a patient opened the electronic pill bottle out of the number of doses prescribed for each bottle in each day, averaged across the study medications and over follow-up.

Secondary Outcome Measures

Change in Uric Acid Level From Baseline
Change in uric acid level from baseline

Full Information

First Posted
February 23, 2021
Last Updated
September 11, 2023
Sponsor
Brigham and Women's Hospital
Collaborators
National Institute on Aging (NIA)
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1. Study Identification

Unique Protocol Identification Number
NCT04776161
Brief Title
Medication Adherence Patterns in Rheumatic Diseases: A Behavioral Trial
Official Title
Using Cues and Rewards in Patients With Arthritis and Rheumatic Disease
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Completed
Study Start Date
August 2, 2021 (Actual)
Primary Completion Date
September 27, 2022 (Actual)
Study Completion Date
November 10, 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
Non-adherence to evidence-based prescription medications results in preventable morbidity and mortality for middle-aged and older adults. Taking medications intended for daily use, like those to prevent or treat chronic conditions, is a repetitive action that has great similarity with other behaviors that must be performed consistently, such as regular exercise, healthy eating, and hand washing. In these cases, people who act consistently do so out of habit. The "repetition-cue-reward" model proposes that habit formation has three central components: behavioral repetition, associated context cues, and rewards. This model has obvious applicability to the daily repetitive activity of medication-taking but has not been tested for this behavior nor adapted as an intervention for patients in real-world care settings. The goal of this pilot study is to evaluate the feasibility and effectiveness of using the repetition-cue-reward model of healthy habit formation to improve medication adherence in patients with arthritis and other rheumatic diseases.
Detailed Description
Non-adherence to evidence-based prescription medications results in preventable morbidity and mortality for middle-aged and older adults. Taking medications intended for daily use, like those to prevent or treat chronic conditions, is a repetitive action that has great similarity with other behaviors that must be performed consistently, such as regular exercise, healthy eating, and hand washing. In these cases, people who act consistently do so out of habit. The "repetition-cue-reward" model proposes that habit formation has three central components: behavioral repetition, associated context cues, and rewards. This model has obvious applicability to the daily repetitive activity of medication-taking but has not been tested for this behavior nor adapted as an intervention for patients in real-world care settings. The goal of this pilot study is to evaluate the feasibility and effectiveness of using the repetition-cue-reward model of healthy habit formation to improve medication adherence in patients with arthritis and other rheumatic diseases. This pilot study will be a 3-arm parallel randomized pragmatic trial comparing medication adherence for adults over 18 years old with arthritis, lupus, or gout who are prescribed 1-3 daily oral medications for this disease. Participants will be randomized to one of three arms for the duration of the study period. Patients in the first intervention arm will choose an event-based cue and receive daily reminder text messages reminding them of their cue. Patients in the second intervention arm will start by establishing their cue and having the donation made, but only those who show no improvement in adherence after 6 weeks will start receiving the text messages. In both interventions arms, a donation will be made to a local charity every time they take their medication. Patients in the control arm will not receive any intervention (but will receive pill bottles to monitor their adherence). Our outcomes of interest will be medication adherence, as measured by electronic pill bottles.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rheumatic Diseases, Gout, Adherence, Medication, Lupus Erythematosus, Systemic

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
62 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
No Intervention
Arm Description
Patients in the control arm will not receive any intervention (but will receive electronic pill bottles to monitor their adherence).
Arm Title
Cue-Reward Intervention
Arm Type
Experimental
Arm Description
Patients in this intervention arm will choose an event-based cue and receive reminder text messages reminding them of their cue. Additionally, a donation will be made to a local charity every time they take their medication.
Arm Title
Cue-Reward Intervention with possible intensification.
Arm Type
Experimental
Arm Description
Patients in this intervention arm will choose an event-based cue. Additionally, a donation will be made to a local charity every time they take their medication. Those who show no improvement in adherence after 6 weeks will start receiving reminder text messages reminding them of their cue.
Intervention Type
Behavioral
Intervention Name(s)
Cue-Reward Intervention
Intervention Description
Patients in the first intervention arm will participate in a goal-setting exercise during which they will identify which habit they want to link their medication-taking to. Patients will also receive text messages reminding them of the habit they decided to link to their medication-taking. Finally, patients will also select a charity to which a donation will be made every time the bottle is opened. The research team will donate $0.50 every day that the patient takes their medication as prescribed. A research assistant will place a sticker with the charity logo under the pill bottle cap so that the patient is reminded of the donation every time they take the medication. Additionally, the patient will receive texts every 4 days summarizing how much money was donated on their behalf.
Intervention Type
Behavioral
Intervention Name(s)
Cue-Reward Intervention with possible intensification
Intervention Description
Patients in the second intervention arm will participate in a goal-setting exercise during which they will identify which habit they want to link their medication-taking to. Finally, patients will also select a charity to which a donation will be made every time the bottle is opened. The research team will donate $0.50 every day that the patient takes their medication as prescribed. A research assistant will place a sticker with the charity logo under the pill bottle cap so that the patient is reminded of the donation every time they take the medication. Additionally, the patient will receive texts every 4 days summarizing how much money was donated on their behalf. After 6 weeks, patients who demonstrate an adherence under 80% to study medications (as measured by the electronic pill bottle) will begin receiving text messages reminding them of their selected cue.
Primary Outcome Measure Information:
Title
Rate of Medication Adherence
Description
Medication adherence will be measured as the percentage of times a patient opened the electronic pill bottle out of the number of doses prescribed for each bottle in each day, averaged across the study medications and over follow-up.
Time Frame
18 weeks
Secondary Outcome Measure Information:
Title
Change in Uric Acid Level From Baseline
Description
Change in uric acid level from baseline
Time Frame
18 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: English-speaking patients receiving their care at a Brigham and Women's Hospital-affiliated rheumatology practice >=18 years of age with rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), or gout prescribed >=1 oral medication for this disease for >=4 months. for patients with gout, had a uric acid level checked in the prior 18 months and the most recent level is >6. for patients with SLE, their most recent c-reactive protein level collected in the past 18 months must be >10. currently have a smartphone with a data plan or WiFi at home 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: Pregnant women Incarcerated individuals
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Candace H Feldman, MD, ScD
Organizational Affiliation
Brigham and Women's Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Brigham and Women's Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
34819291
Citation
Fontanet CP, Choudhry NK, Wood W, Robertson T, Haff N, Oran R, Sears ES, Kim E, Hanken K, Barlev RA, Lauffenburger JC, Feldman CH. Randomised controlled trial targeting habit formation to improve medication adherence to daily oral medications in patients with gout. BMJ Open. 2021 Nov 24;11(11):e055930. doi: 10.1136/bmjopen-2021-055930.
Results Reference
derived

Learn more about this trial

Medication Adherence Patterns in Rheumatic Diseases: A Behavioral Trial

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