Reducing Disparities in Medication Adherence in SLE
- Conditions
- Systemic Lupus Erythematosus
- Interventions
- Behavioral: Behavioral Intervention
- Registration Number
- NCT03738826
- Lead Sponsor
- Duke University
- Brief Summary
This is a pilot study to assess the feasibility of using Surescripts refill data during the clinical encounter to improve medication adherence in patients with systemic lupus erythematosus
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 135
Not provided
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Intervention arm Behavioral Intervention Lupus clinic providers will use Surescripts refill information to assess adherence level and address adherence barriers. We will assess the feasibility and acceptability of the intervention.
- Primary Outcome Measures
Name Time Method Acceptability as Measured by Provider Survey 12 weeks Acceptability as measured by provider survey, score range 1-5, with a higher score indicating that the intervention was more acceptable.
Feasibility as Measured by Number of Participants With EMR (Electronic Medical Record) Documentation of Adherence 12 weeks Feasibility as measured by documentation of adherence assessment made by provider.
- Secondary Outcome Measures
Name Time Method Percentage of Adherent Participants as Determined by Medication Possession Ratio (MPR) Baseline, 12 weeks Medication Possession Ratio (MPR) = days with medication/total days. This will be determined by pharmacy refill data and calculated for 3 months (90 days). An MPR \> or = 80% indicates adherence.
Medication Adherence as Determined by Self Report 12 weeks
Trial Locations
- Locations (1)
Duke University
🇺🇸Durham, North Carolina, United States