A Socio-ecological Approach for Improving Self-management in Adolescents With SCD
Who can join
As published by the study on ClinicalTrials.gov. "Not stated" means the study hasn't said — ask the study team.
- Age
- 13 Years to 21 Years
- Sex
- All sexes
- Healthy volunteers
- Not accepted
- Compensation
- Not stated
Other requirements are listed under Eligibility below. Only the study team can confirm whether you can join.
What to expect
No one can promise a trial will help you personally — that is what the research is trying to find out.
What participation involves
- Procedures mentioned: Questionnaires
Only what the study's summary and detailed description on ClinicalTrials.gov say. Time periods may describe the whole study or a part of it — ask the study team what applies to you.
Show the study's own words
- "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)."
- Compensation
- Not stated
- Study-related exams and procedures are typically provided at no cost. This is how many trials work in general — confirm the details for this study with the study team.
- Participants are monitored closely by the research team throughout the study.
- Some participants may receive access to an investigational treatment, which is still being studied.
- Your participation helps researchers learn whether this approach could help future patients.
About this study
In plain language
This study tests SCThrive, an 8-week online group program with a mobile app, for people ages 13–21 with sickle cell disease. It looks at whether the program helps them take charge of their care, manage daily life, and have fewer emergency room visits. Researchers will compare it with usual care plus educational text messages and check whether benefits last 3 months.
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.
Compensation is read from the study's own description and may be missing — always confirm with the study team.
Eligibility
Who can join
- Receive care at a sickle cell clinic taking part in the study.
- Have a confirmed diagnosis of sickle cell disease.
- Be 13–21 years old.
Who can't join
- Have another long-term illness that would make it hard to measure how well you take charge of your care.
- Do not speak English.
- Have a thinking or mental health condition that your doctor or study therapists believe would make it hard to take part.
Simplified for readability. The official criteria below are what the study team uses.
Official eligibility criteria
Inclusion Criteria: * Patient of a participating SCD Clinic * Confirmed diagnosis of SCD * 13-21 years of age Exclusion Criteria: * Another chronic disease (which would complicate measurement of patient activation) * Non-English-speaking * Cognitive or psychiatric disorder that the physician or study therapists believe would impair study participation.
Study sites (4)
DE
- Nemours Children's Health · Wilmington, DE 19803Benjamin Bear, MSW · Study contact · 302-723-9331 · benjamin.bear@nemours.orgAimee Hildenbrand, PhD · Principal investigatorMore trials in Wilmington
GA
- Children's Healthcare of Atlanta · Atlanta, GA 30303Vontarius Howard · Study contact · 404-785-3245 · Vontarius.Howard@choa.orgSoumitri Sil, PhD · Principal investigatorMore trials in Atlanta
OH
- Cincinnati Children's Hospital Medical Center · Cincinnati, OH 45229Lori Crosby, PsyD · Study contact · 513-636-5380 · lori.crosby@cchmc.orgAma Wilson, MPH · Study contact · 513-803-0917 · ama.wilson@cchmc.orgLori Crosby, PsyD · Principal investigatorMore trials in Cincinnati
PA
- Children's Hospital of Philadelphia · Philadelphia, PA 19104Polina Poliakova · Study contact · 267-426-0355 · poliakovap@chop.eduLisa Schwartz, PhD · Principal investigatorMore trials in Philadelphia