Gout Clinical Trial
Official title:
Using Cues and Rewards in Patients With Arthritis and Rheumatic Disease
Verified date | September 2023 |
Source | Brigham and Women's Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
Status | Completed |
Enrollment | 62 |
Est. completion date | November 10, 2022 |
Est. primary completion date | September 27, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 85 Years |
Eligibility | 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 |
Country | Name | City | State |
---|---|---|---|
United States | Brigham and Women's Hospital | Boston | Massachusetts |
Lead Sponsor | Collaborator |
---|---|
Brigham and Women's Hospital | National Institute on Aging (NIA) |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | 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. | 18 weeks | |
Secondary | Change in Uric Acid Level From Baseline | Change in uric acid level from baseline | 18 weeks |
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