Using a smartphone app to help patients with knee osteoarthritis stick to their exercise routines
Effectiveness of the ARTH-e Application on Adherence to Physical Exercises in Patients Suffering From Knee Osteoarthritis: Randomized Controlled Trial (ARTHe 3)
This study is testing whether a smartphone app can help people with knee osteoarthritis stick to their exercise routines better than regular care.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 120 (estimated) |
| Ages | 40 Years to 85 Years |
| Sex | All |
| Sponsor | University Hospital, Clermont-Ferrand Academic / other |
| Locations | 4 sites (Clermont-Ferrand and 3 other locations) |
| Trial ID | NCT06359171 on ClinicalTrials.gov |
What this trial studies
This study investigates the effectiveness of the ARTH-e smartphone application in improving adherence to physical exercises among patients with knee osteoarthritis compared to standard care. Participants will be assessed using various questionnaires, including the EARS questionnaire, to evaluate changes in adherence and other health-related metrics. The study aims to leverage e-health technology to enhance patient engagement and support in managing their condition. By utilizing a mobile application, the study seeks to provide a tailored approach to therapeutic education and exercise adherence.
Who should consider this trial
Good fit: Ideal candidates are adults aged 40 to 85 with symptomatic knee osteoarthritis who own a smartphone or tablet.
Not a fit: Patients who have undergone knee surgery, have inflammatory rheumatism, or face medical contraindications to physical activity may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly improve exercise adherence and overall management of knee osteoarthritis for patients.
How similar studies have performed: Previous studies have shown promise in using smartphone applications for chronic conditions, indicating potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients aged between 40 and 85 years with uni or bilateral knee osteoarthritis according to EULAR (European League Against Rheumatism) criteria, symptomatic and diagnosed prior to inclusion by a specialist or not. * Having an involvement of at least one knee. * Own a smartphone or tablet running at least Android 5 or iOS 11. * Able to give written consent to participate in the study. * Beneficiary of a social security plan. Exclusion Criteria: * pregnant or breast-feeding women Patients under legal protection measures (guardianship, curatorship or protection of the court) * Patients who have undergone knee surgery (total or partial prosthesis, tibial transposition surgery, arthrodesis) * Patients with inflammatory rheumatism * Patients with neurological sequelae * Contraindications to physical activity for medical reasons * Patients with difficulties in understanding the French language * Refusal to participate * Patients who have already participated in the ARTH-e 2 study or who are already included in a research protocol that could influence the current protocol
Where this trial is running
Clermont-Ferrand and 3 other locations
- CHU Clermont-Ferrand — Clermont-Ferrand, France (Recruiting)
- CH Emile Roux — Le Puy-en-Velay, France (Not_yet_recruiting)
- CHU Montpellier — Montpellier, France (Not_yet_recruiting)
- CHU Nantes — Nantes, France (Not_yet_recruiting)
Study contacts
- Study coordinator: Lise Laclautre
- Email: promo_interne_drci@chu-clermontferrand.fr
- Phone: 04 73 75 11 95
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.