Tele-Rehabilitation in Adults With Cystic Fibrosis

Sponsor
King Saud University
Study ID
NCT07500493
Status
Not Yet Recruiting

Notify me when recruiting opens

Save your spot on the interest list for this study. We'll keep your details with this study so our team can follow up when recruiting opens.

Not yet recruiting

Add your contact details and location so we can keep your interest tied to this study.

Conditions

  • Cystic Fibrosis
  • Frailty
  • Sarcopenia

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Tele-Rehabilitation Exercise Program — BEHAVIORAL
    An 8-week tele-rehabilitation program consisting of supervised aerobic and resistance exercise sessions delivered remotely three times per week using video communication. The program includes individualized exercise prescription and progressive adjustment based on participant tolerance and clinical status. Sessions are conducted by trained rehabilitation personnel following established pulmonary rehabilitation guidelines.

Study Details

This study is a randomized controlled trial designed to evaluate the effectiveness of an 8-week tele-rehabilitation program in adults with cystic fibrosis. Cystic fibrosis is a chronic condition that affects the lungs and can lead to reduced muscle mass, physical weakness, frailty, and decreased quality of life. Participants will be randomly assigned to either a tele-rehabilitation group or a usual care group. The tele-rehabilitation program includes supervised exercise sessions conducted remotely three times per week using video communication. The program combines aerobic and resistance training based on established rehabilitation guidelines. The primary aim of the study is to assess the effect of the program

Key Dates

First listed
Mar 30, 2026
Start date
Apr 17, 2026
Status verified
Mar 2026
Primary completion
Jun 17, 2026
Completion
Jul 17, 2026

Study Design

Enrollment
76 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Tele-Rehabilitation Group
    Participants will receive an 8-week tele-rehabilitation program consisting of supervised aerobic and resistance exercise sessions delivered remotely three times per week. The program will be individualized and progressively adjusted based on participant tolerance and clinical status.
  • No Intervention: Usual Care Group
    Participants will continue receiving standard clinical care without participation in the tele-rehabilitation program during the study period.

Primary Outcome Measure

Fat-Free Mass Index (FFMI) [ Time Frame: Baseline to Week 8 (end of intervention) ]

Central Contacts

Related Studies