NCT06457451Recruiting
Impact of a Coordinated Dietetic-adapted Physical Activity Program on the Percentage of Lean Body Mass in Adults With Cystic Fibrosis Treated With Elexacaftor-Tezacaftor-Ivacaftor: Multicentre Randomised Controlled Trial
Impact d'un Programme coordonné diététique-activité Physique adaptée Sur le Pourcentage de Masse Maigre d'Adultes Atteints de Mucoviscidose traités Par Elexacaftor-Tezacaftor-Ivacaftor : Essai contrôlé randomisé Multicentrique
Source: ClinicalTrials.gov · Last updated 1 Dec 2025
Brief summary (registry, in English)
Cystic fibrosis is an autosomal recessive inherited disease linked to various mutations in the gene coding for the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) protein, with respiratory and digestive disorders conditioning the prognosis. Digestive damage may be responsible for malnutrition of multifactorial origin (insufficient energy intake, increased energy losses, increased basal metabolic rate), and studies show a correlation between reduced lean body mass and respiratory function. In 2019, the French National Authority for Health (HAS) redefined undernutrition by including "quantified reduction in muscle mass and/or function" as a phenotypic diagnostic criterion. Elexacaftor-Tezacaftor-Ivacaftor, an innovative therapy (authorization in 2021) for this population, aims to restore the function of CFTR protein. Significant improvements in lung function and weight gain were observed from the first weeks of treatment. These improvements have also led to the emergence of lesser-known nutritional problems in these patients, such as overweight and the development of metabolic complications. Nonetheless, new management options in terms of dietary adjustments and adapted physical activity for these patients are possible, given the development of their abilities. Adapted Physical Activity (APA) helps to improve general muscular function by strengthening respiratory and skeletal muscles, improving aerobic capacity, and aiding bronchial drainage through muscle strengthening and endurance work. Maintaining or even increasing muscle mass depends not only on appropriate food intake and optimal dietary management, but also on regular physical activity, as recommended by the HAS. Our hypothesis is therefore that a structured dietetic/adapted physical activity program (DIAPASOM program) can increase the percentage of lean body mass at 12 months in adult cystic fibrosis patients treated with Elexacaftor-Tezacaftor-Ivacaftor.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 100 (estimated)
- First submitted
- 7 Jun 2024
- Start date
- 25 Nov 2024
- Primary completion date
- 30 Nov 2027
- Lead sponsor
- University Hospital, Tours
- Diseases
- Cystic fibrosis
- NCT number
- NCT06457451
What you commit to
- Study type: Interventional
- Planned participants: 100
- From 25 Nov 2024 to the primary completion date, 30 Nov 2027
- 4 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other
- Pregnant and breast-feeding women
- Subject under legal protection, guardianship or curatorship
- Subject whose physical activity is not medically authorised or whose physical and motor capacities do not allow them to take part in physical activity.
- Subject who is unable to comply with the requirements of the DIAPASOM program
- Difficulty in understanding the self-questionnaires
- Wearing a pacemaker or metal prosthesis
- Fluid retention
Who the study is looking for
- Subject aged 18 or over
- Suffering from cystic fibrosis
- Treated with Elexacaftor-Tezacaftor-Ivacaftor for at least 6 months
- Affiliated to a social security scheme
- with a signed Informed Consent form.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (4)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Cystic Fibrosis Resource and Competence Centre, University Hospital, Angers Coordinator of this site? Confirm its status | Angers | France | Recruiting |
| Cystic Fibrosis Resource and Competence Centre, Fondation Ildys, Roscoff Coordinator of this site? Confirm its status | Roscoff | France | Recruiting |
| Cystic Fibrosis Resource and Competence Centre, University Hospital, Tours Coordinator of this site? Confirm its status | Tours | France | Recruiting |
| Cystic Fibrosis Resource and Competence Centre, Hospital, Tours Coordinator of this site? Confirm its status | Vannes | France | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.