Actively Recruiting

Phase Not Applicable
Age: 13Years - 21Years
All Genders
NCT06290401

A Socio-ecological Approach for Improving Self-management in Adolescents With SCD

Led by Children's Hospital Medical Center, Cincinnati · Updated on 2026-05-11

310

Participants Needed

4

Research Sites

177 weeks

Total Duration

On this page

Sponsors

C

Children's Hospital Medical Center, Cincinnati

Lead Sponsor

N

Nemours Children's Health System

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this clinical trial is to evaluate the impact of SCThrive (a behavioral self-management intervention) on patient activation, self-management behaviors, daily functioning, and emergency room visits in 260 adolescents and young adults with sickle cell disease (SCD) ages 13-21 receiving care at 1 of 4 pediatric SCD clinics. The main question\[s\]it aims to answer are: * Does SCThrive improve patient activation? * Does SCThrive improve self-management behaviors, daily functioning, and decrease emergency room visits? * Are any improvements maintained 3 months after treatment? Participants will complete self-management related surveys before, after, and 3 months following their participation in an 8- week, virtual group intervention with an accompanying mobile app (SCThrive). Researchers will compare outcomes for participants who receive SCThrive and participants who receive uniform standard care (SCHealthED which = standard of care plus SCD educational text messages) to see if there are differences in patient activation, self-management behaviors, daily functioning, and emergency room visits.

CONDITIONS

Official Title

A Socio-ecological Approach for Improving Self-management in Adolescents With SCD

Who Can Participate

Age: 13Years - 21Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient of a participating SCD Clinic
  • Confirmed diagnosis of SCD
  • 13-21 years of age
Not Eligible

You will not qualify if you...

  • Presence of another chronic disease that would complicate measurement of patient activation
  • Non-English-speaking
  • Cognitive or psychiatric disorder that the physician or study therapists believe would impair study participation

AI-Screening

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Trial Site Locations

Total: 4 locations

1

Nemours Children's Health

Wilmington, Delaware, United States, 19803

Not Yet Recruiting

2

Children's Healthcare of Atlanta

Atlanta, Georgia, United States, 30303

Not Yet Recruiting

3

Cincinnati Children's Hospital Medical Center

Cincinnati, Ohio, United States, 45229

Actively Recruiting

4

Children's Hospital of Philadelphia

Philadelphia, Pennsylvania, United States, 19104

Not Yet Recruiting

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Research Team

A

Ama Wilson, MPH

CONTACT

T

Taylor Richardson, BA

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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