Evaluating CVD Medication Adherence Program in Low SES
Completed · Not applicable
Conditions studied: Cardiovascular Disease, Hypertension, Diabetes
In brief
The investigators propose to evaluate the implementation of an efficacious medication adherence program in a group at high risk for CVD. The program involves patients receiving/responding to e-reminders to take CVD medications via patient-selected technology \[mobile/web-based applications, short message service (SMS; text messaging), interactive voice response (IVR), or e-mail\] supported by a tailored, monthly, self-management program administered by either research staff or a case manager staff member from the Duke Outpatient Clinic via the telephone. This is a hybrid type II implementation science study.
Key facts
- Study ID
- NCT02375737
- Run by
- Duke University
- People needed
- 100
- Starts
- 2015-01-01
- Expected to finish
- 2016-08-01
- Last updated by the study team
- 2016-08-12
Who can join
Age: 21 and older, up to 85. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Medicaid recipient (preferred); however the investigators will include those patients with other types of insurance or those who are uninsured
- Enrolled in Duke Outpatient Clinic for at least one year
- Outpatient diagnostic code for hypertension and/or hypercholesterolemia and/or diabetes
- Poorly controlled BP levels (>140/90) and/or LDL-C (>130mg/dl) and/or HbA1c of >8 within last 6 months
You may not qualify if…
- No access to cell phone
- Not proficient in English
- Nursing home/long-term care facility resident or receiving home health care
- Impaired hearing/ speech/ vision
- Participating in another trial (pharmaceutical or behavioral)
- Planning to leave the area in the next 12 months
- Pregnancy (or planning)
- Diagnosis of life-threatening disease with death probable within 1 year
- Active Diagnosis of psychosis or dementia (has been hospitalized in the last 30 days)
- Diagnosis of ESRD
Where it is running
- Duke University Health System Clinic — Durham, North Carolina, United States
Full record on ClinicalTrials.gov
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