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Reducing Disparities in Medication Adherence in SLE

Not Applicable
Completed
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
Inclusion Criteria

Not provided

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Exclusion Criteria

Not provided

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Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Intervention armBehavioral InterventionLupus 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
NameTimeMethod
Acceptability as Measured by Provider Survey12 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 Adherence12 weeks

Feasibility as measured by documentation of adherence assessment made by provider.

Secondary Outcome Measures
NameTimeMethod
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 Report12 weeks

Trial Locations

Locations (1)

Duke University

🇺🇸

Durham, North Carolina, United States

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