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Clinical Trials/NCT04688411
NCT04688411
Recruiting
N/A

An mHealth Strategy to Improve Medication Adherence in Adolescents With Sickle Cell Disease

Ann & Robert H Lurie Children's Hospital of Chicago1 site in 1 country40 target enrollmentSeptember 28, 2020

Overview

Phase
N/A
Intervention
Not specified
Conditions
Sickle Cell Disease
Sponsor
Ann & Robert H Lurie Children's Hospital of Chicago
Enrollment
40
Locations
1
Primary Endpoint
Percentage of patients achieving feasibility criteria of using the MED-Go app
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

The primary objective of this study is to evaluate a potential behavioral intervention (MED-Go app). To meet this objective, the researchers will conduct a pilot randomized controlled trial to test the feasibility and acceptability of MED-Go app in adolescents and young adults (AYA) with sickle cell disease (SCD). The long-term goal of this research is to promote medication adherence behavior and improve health outcomes in AYA with SCD.

Detailed Description

Sickle cell disease is the most common genetic disorder in the US, affecting about 100,000 Americans, and about 1 in 400 African American live births, incurring annual health care costs of $335 million. SCD can lead to serious complications including unpredictable, debilitating pain episodes, cardiopulmonary disease, stroke, and long-term end organ damage.These complications lead to significant declines in health-related quality of life (HRQOL) and other patient-reported outcomes (PROs), culminating in early mortality, particularly among AYA. Hydroxyurea (HU), at present, is the main FDA approved medication for SCD that reduces morbidity and mortality, improves HRQoL and lowers healthcare utilization.However, adherence to HU remains suboptimal with only 35-50% of patients achieving high adherence (≥90%), particularly among AYA with SCD. Low HU adherence has been associated with worse health outcomes, poor HRQOL and increased healthcare utilization. Low HU adherence is multifactorial, especially in AYA with other competing priorities and vulnerability in developmental and psychological factors contributing to adherence behavior. AYA have adopted text messaging and smartphone apps at a fast pace, including those who have SCD.Existing evidence indicates that mobile health (mHealth) behavioral interventions are feasible and acceptable with modest efficacy at improving medication adherence and self-management in AYA, including SCD. The specific aim for this study is to test the feasibility and acceptability of the MED-Go app as an mHealth behavioral intervention to improve HU adherence among AYA with SCD.

Registry
clinicaltrials.gov
Start Date
September 28, 2020
End Date
February 1, 2025
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Sherif Badawy, MD

Assistant Professor, Department of Pediatrics, Division of Hematology, Oncology and Stem Cell Transplant

Ann & Robert H Lurie Children's Hospital of Chicago

Eligibility Criteria

Inclusion Criteria

  • Age 12-21 years old
  • Any sickle cell disease genotype
  • On steady state of hydroxyurea for 2 months
  • Own of have access to a smartphone during the study period

Exclusion Criteria

  • Recent hospitalizations within the past 7 days

Outcomes

Primary Outcomes

Percentage of patients achieving feasibility criteria of using the MED-Go app

Time Frame: 12 weeks

Feasibility is defined as 70% of participants logging their daily HU 70% of the time over 12 weeks or 59 out of 84 study days. This will be reported as a dichotomous outcome, either yes or no.

Secondary Outcomes

  • Scores of System Usability Scale (SUS)(12 weeks)
  • Hydroxyurea adherence rates(12 weeks)

Study Sites (1)

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