RECRUITING

Intervention to Improve Communication and Medication Adherence in Lupus

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

CO-LEAD is an intervention to improve patient-provider communication and medication adherence among patients with systemic lupus erythematosus (SLE). The purpose of this study is to optimize the culturally appropriate delivery and test the effect of the CO-LEAD intervention, which includes the following: 1. clinicians will be provided with a program to teach them to use effective communication strategies with patients to review real-time pharmacy refill date, engage and formulate solutions to adherence barriers, and collaboratively overcome adherence barriers. 2. use of a reliable and valid patient-reported measure of the extent of and reasons for nonadherence that helps patients identify and communicate their adherence barriers with clinicians proactively, efficiently, and comprehensively.

Official Title

Intervention to Improve Patient-provider Communication and Medication Adherence Among Patients With Systemic Lupus Erythematosus (SLE)

Quick Facts

Study Start:2024-06-30
Study Completion:2028-12
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06458075

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 90 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Adult rheumatology attendings, advanced practice providers, and fellows at the two academic institutions
  2. 2. Clinicians who have ambulatory rheumatology care at least ½ day per week
  1. 1. Clinicians at Duke University who were involved in the investigators' pilot work
  2. 2. Clinicians with an anticipated departure from the institution in the 12 months following enrollment

Contacts and Locations

Study Contact

Kai Sun, MD
CONTACT
919- 681- 7417
kai.sun@duke.edu
Kathyrn Pollak, PhD
CONTACT
919-681-4757
Kathyrn.Pollak@duke.edu

Principal Investigator

Kai Sun, MD
PRINCIPAL_INVESTIGATOR
Duke University

Study Locations (Sites)

Duke University
Durham, North Carolina, 27710
United States

Collaborators and Investigators

Sponsor: Duke University

  • Kai Sun, MD, PRINCIPAL_INVESTIGATOR, Duke University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-06-30
Study Completion Date2028-12

Study Record Updates

Study Start Date2024-06-30
Study Completion Date2028-12

Terms related to this study

Additional Relevant MeSH Terms

  • Systemic Lupus Erythematosus