Home-based exercise program for lymphoma survivors
Remotely Monitored Rehabilitation in Hemato-oncological Survivors After Treatment: The Tele@Home Study
NA · Brno University Hospital · NCT05779605
This study is testing a 12-week home exercise program with online support for lymphoma survivors to see if it helps them get fitter and feel better compared to traditional gym workouts.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 80 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Brno University Hospital (other) |
| Drugs / interventions | chemotherapy |
| Locations | 1 site (Brno) |
| Trial ID | NCT05779605 on ClinicalTrials.gov |
What this trial studies
This study investigates the effectiveness of a 12-week home-based exercise training program with remote guidance and telemonitoring compared to traditional center-based training for lymphoma survivors. It aims to evaluate improvements in cardiorespiratory fitness, physical activity levels, and overall quality of life among participants post-treatment. The study will enroll 80 patients and assess various outcomes, including peak oxygen consumption and adherence to exercise prescriptions, at baseline, after 12 weeks, and one year later. The goal is to enhance long-term motivation and effectiveness of independent training in cancer survivors.
Who should consider this trial
Good fit: Ideal candidates are lymphoma survivors who have recently completed chemotherapy and are clinically stable.
Not a fit: Patients with acute heart disease, severe psychological or cognitive disorders, or those currently engaged in supervised exercise programs may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly improve the physical fitness and quality of life for lymphoma survivors.
How similar studies have performed: Other studies have shown positive outcomes with home-based exercise interventions for cancer survivors, suggesting this approach may be effective.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: Participants * with hemato-oncological malignancy / lymphoma (in last two months) * after cancer systemic chemotherapy-based treatment * with clinically stable state * with the ability to perform a cardiopulmonary exercise test * with the ability to understand and write in the Czech language * with an internet connection at home * literacy with information and communication technology Exclusion Criteria: Participants * with acute heart disease or decompensation in the previous six weeks, * with psychological severe, cognitive disorders, * serious training limitations (musculoskeletal disorders) * currently carried out the recommendations for physical activity (150min per week) * who take part in a training program under supervision elsewhere
Where this trial is running
Brno
- University Hospital Brno — Brno, Czechia (RECRUITING)
Study contacts
- Principal investigator: Ladislav Batalik — Department of Rehabilitation, University Hospital Brno, Czech Republic
- Study coordinator: Katerina Filakova
- Email: filakova.katerina@fnbrno.cz
- Phone: 00420532233123
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.
Conditions: Hematologic Malignancy, Lymphoma