Video telehealth exercise training for cystic fibrosis patients
Video Telehealth Exercise Training in Cystic Fibrosis
This study is testing a video-based exercise program for people with cystic fibrosis to see if it helps them feel better during flare-ups.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 25 (estimated) |
| Ages | 19 Years and up |
| Sex | All |
| Sponsor | University of Alabama at Birmingham Academic / other |
| Locations | 1 site (Birmingham, Alabama) |
| Trial ID | NCT04680403 on ClinicalTrials.gov |
What this trial studies
This study aims to implement an exercise program for patients with cystic fibrosis experiencing an exacerbation. It will enroll 25 patients who will participate in a tailored exercise regimen delivered through a data-enabled smartphone with video capabilities. The intervention includes supervised exercise sessions and behavior change coaching over a 12-week period, with follow-ups at 3 and 6 months to ensure adherence and sustainability. The approach utilizes interactive video conferencing to facilitate real-time support and engagement.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older with a diagnosis of cystic fibrosis who are clinically stable and have not experienced an exacerbation in the past six weeks.
Not a fit: Patients with comorbidities that prevent them from exercising will not benefit from this study.
Why it matters
Potential benefit: If successful, this program could improve exercise adherence and overall health outcomes for patients with cystic fibrosis.
How similar studies have performed: Other studies have shown success with telehealth interventions in chronic conditions, suggesting potential for this approach in cystic fibrosis.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: Diagnosed with Cystic Fibrosis 18 years old and older clinically stable with no exacerbation within 6 weeks Exclusion Criteria: any comorbidity that precludes exercise -
Where this trial is running
Birmingham, Alabama
- University of Alabama at Birmingham — Birmingham, Alabama, United States (Recruiting)
Study contacts
- Principal investigator: Stefanie Krick — University of Alabama at Birmingham
- Study coordinator: Heather Hathorne
- Email: hhathorne@peds.uab.edu
- Phone: 205-638-9568
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.