Prader-Willi Syndrome Body Composition

Status Recruiting

Clinical Trial Summary

Adults aged over 18 years, with the diagnosis of Prader-willi syndrome will be recruited through the hospital's outpatient clinic for either as intervention group receiving therapeutic elastic band training, or as control group receiving usual care for a total of 16 weeks. Body composition, physical capacity, and serum changes will be assessed before and after the intervention.

Clinical Trial Description

Participants that fulfill the inclusion criteria will be assigned into one of the two arms: elastic band intervention group (EB) or control group (CG). Both groups will received a baseline: dual X-ray absorptiometry body composition, physical capacity, and serum markers examinations. EB will then receive a 16-week progressive elastic band resistance exercise training, while the CG will receive usual care. After the 16 weeks from the baseline assessment, a followed-up: dual X-ray absorptiometry body composition, physical capacity, and serum examinations will be assessed. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04597645
Study type	Interventional
Source	Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation
Contact	Valeria Chiu, M.D
Phone	+886-266289779
Email	haydenbell28@gmail.com
Status	Recruiting
Phase	N/A
Start date	May 6, 2020
Completion date	July 31, 2021

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