Hospital hopes new program can break weight gain cycle in rare genetic disorder
NCT ID NCT05249998
Summary
This study tested a new 5-week hospital program designed to help adults with Prader-Willi syndrome, a rare genetic disorder that causes constant hunger and leads to severe obesity. The program combined tailored physical activity, nutrition guidance, and education workshops. Researchers compared this intensive program to standard hospital care for 128 patients to see if it helped them better control their weight and health behaviors for six months after going home.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes NO responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for OBESITY are added.
By submitting, you agree to our Terms of use
Contacts and locations
Show contact details
Enter your email to view the contact information for this study.
By submitting, you agree to our Terms of use
Locations
-
Service diététique Hôpital Marin d'Hendaye- AP-HP
Hendaye, 64701, France
Conditions
Explore the condition pages connected to this study.