NCT07440433Pas encore en recrutement
Home-Based Physiotherapy in Oncology
Résumé
The goal of this clinical trial is to assess the feasibility, acceptability, and safety of a supervised home-based physiotherapy programme for adult oncology patients. The programme combines aerobic cycling exercise, resistance training, and mental preparation strategies, delivered at home with regular professional supervision. The main questions this study aims to answer are: Is a 6-month supervised home-based physiotherapy programme feasible in terms of recruitment, adherence, and retention? Is the programme safe for oncology patients undergoing or having recently completed cancer treatment? Is the programme acceptable and satisfactory from the patient's perspective? How do physical function and health-related quality of life change over the course of the programme? This is a single-arm feasibility study with no comparison group. Participants will: Receive a stationary exercise bike delivered and installed at their home Follow a 6-month individualized physiotherapy programme including: Three weekly sessions combining moderate-intensity cycling and resistance exercises Wear a connected activity watch during exercise sessions to monitor heart rate and exercise duration Receive weekly supervision from oncology-trained physiotherapists through alternating in-person hospital visits and structured phone calls Complete physical function assessments and questionnaires on quality of life, fatigue, and programme satisfaction at baseline, mid-program, and study completion The results of this study will inform the design of a future larger controlled trial and contribute to the development of accessible home-based rehabilitation programmes for oncology patients.
Critères d'inclusion
• Age ≥ 18 years • Diagnosis of solid cancer, undergoing or recently completed treatment. • Overall survival greater than 12 months, as judged by the treating oncologist • Clinically stable and deemed fit for moderate exercise by the treating oncologist • Able to use an exercise bike • Home environment suitable for delivery and installation of the exercise bike • Able to understand the study language and follow study instructions • Able to give a written informed consent
Critères d'exclusion
• Medical contraindication to moderate exercise (e.g. uncontrolled cardiac or pulmonary disease, recent myocardial infarction, severe anemia or acute infection, unstable bone metastases or high fracture risk) • Cognitive impairment preventing active participation • Physical inability to perform the prescribed exercise programme, including cycling and resistance exercises. • Participation in another intensive rehabilitation program • Any other condition that, in the opinion of the treating oncologist or investigator, makes participation unsafe or not feasible • Pregnant or lactating women.
Contacts
Les coordonnées de l'équipe de l'essai s'affichent sur demande.
Voir la fiche officielle de l'essai- Statut
- Pas encore en recrutement
- Phase
- Sans phase (N/A)
- Type d'étude
- Interventionnelle
- Pays
- Suisse
- Promoteur
- University Hospital, Geneva(Autre)
- N° de protocole
- PRADA-HUG
- Pathologies
- Rehabilitation Exercise, Oncologic Diseases
- Interventions
- Comportemental
Traitements évalués
- Home-based cycling + resistance training with physiotherapist supervision
Lieux · 1
- Geneva, SuisseHUGRecrutement pas encore ouvert dans ce centre
Au total, dans le monde, le seul centre listé au registre est prévu ; le recrutement n'est pas encore ouvert.
Statut par centre selon le registre ClinicalTrials.gov (dernière mise à jour publiée : 27 février 2026).
Ce statut peut avoir changé et ne dit rien de votre éligibilité : avant toute démarche, vérifiez avec votre oncologue ou le centre.
Voir aussi
Autres versions
Ces résultats sont indicatifs et ne remplacent pas un avis médical — à discuter avec votre médecin.