Respiratory Training in Friedreich's Ataxia
Completed · Not applicable
Conditions studied: Friedreich Ataxia
In brief
This is a prospective interventional study of patients with Friedreich's Ataxia that receive respiratory strength training for a period of 12 weeks with two research visits at the beginning and at the end of the study period. Visits include swallowing evaluation with fiberoptic endoscopic evaluation of swallowing, pulmonary function testing, surface electromyography and patient surveys.
Key facts
- Study ID
- NCT06539598
- Run by
- University of Florida
- People needed
- 1
- Starts
- 2024-08-29
- Expected to finish
- 2025-08-07
- Last updated by the study team
- 2025-11-03
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- confirmed genetic testing of Friedreich's Ataxia
- have an overall DIGEST score of 1 or higher based on FEES screening
- are able to perform pulmonary function testing
You may not qualify if…
- have been on antibiotics within 15 days prior to baseline screening.
- have been prescribed systemic corticosteroids or neuromuscular blocking agents within 15 days of the baseline screening
- have an allergy or contraindication to topical lidocaine or oxymetazoline
- have any other concurrent medical condition which, in the opinion of the investigators, would make the subject inappropriate to participate in testing or respiratory exercise
Where it is running
- Clinical Research Center — Gainesville, Florida, United States
Full record on ClinicalTrials.gov
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