New program aims to smooth healthcare transition for teens with rare hormone disorder
NCT ID NCT07611786
First seen Jun 27, 2026 · Last updated Aug 21, 2026 · Updated 5 times
Summary
This study tests a structured program to help 40 adolescents and young adults with congenital adrenal hyperplasia (CAH) move from pediatric to adult healthcare. Participants will learn about their condition, emergency preparedness, and self-management. The goal is to see if the program improves their readiness, knowledge, and quality of life during this important transition.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
-
About 40 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
-
Oct 2026
An estimate. Start dates often move.
- Expected to finish
-
Oct 2029
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
This population will be recruited from our pediatric endocrinology clinic as available.
- Ages
-
16 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: YA Participants * Diagnosis of congenital adrenal hyperplasia (any subtype or severity) * Age ≥16 years * Active follow-up within the pediatric endocrinology clinic * English-speaking * Cognitively able to complete questionnaires with or without assistance * Anticipated ability to participate in CAH-T visits during the study period Caregiver Participants * Parent, guardian, or primary support person of an enrolled AYA participant Provider Participants * Pediatric endocrinologists, nurse practitioners, or transition-related clinical staff involved in CAH care for at least 6 months Exclusion Criteria: * Significant cognitive impairment precluding participation * Inability to complete study procedures * Inability to provide informed consent/assent
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Congenital adrenal hyperplasia are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
1 site. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
-
University of Alabama at Birmingham
Birmingham, Alabama, 35233, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can a Timed-Release hydrocortisone pill match the Body's overnight hormone rhythm?
- Can a modified hydrocortisone mimic the Body's natural cortisol rhythm?
- Can a Twice-Daily hormone pill match standard care for CAH?
- Could a simple saliva test replace blood draws for hormone monitoring?
- New hope for CAH: drug may slash steroid use
- New hope for toddlers with rare hormone disorder?