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A Universal Medication Schedule to Promote Adherence to Complex Drug Regimens

NCT02820753 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 677

Last updated 2022-02-01

Study results available
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Summary

This study will leverage available technologies and test strategies to impart the Universal Medication Schedule (UMS) in primary care to help patients understand, consolidate, safely use, and adhere to their complex medication regimens.

Conditions

  • Adherence

Interventions

BEHAVIORAL

EHR + (Text or Portal)

Per protocol analysis: Patients who received the initial 6 weeks of SMS messaging continuously, or logged on to the patient portal and completed at least one survey.

Sponsors & Collaborators

  • University of North Carolina

    collaborator OTHER

  • Emory University

    collaborator OTHER

  • Vanderbilt University

    collaborator OTHER

  • Northwestern University

    lead OTHER

Principal Investigators

  • Michael S Wolf, PHD · Northwestern University

  • Stacy C Bailey, PHD · Northwestern University

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
FACTORIAL

Eligibility

Min Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-04-03
Primary Completion
2020-09-21
Completion
2020-09-21

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02820753 on ClinicalTrials.gov