Online exercise and education program for cancer patients
Effect of a Telerehabilitation-exercise Intervention in Oncology Patients in the Covid-19 Pandemic
This study tests whether an online exercise and education program can help cancer patients and survivors improve their physical health and quality of life while managing symptoms like fatigue.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 30 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | University of Malaga Academic / other |
| Locations | 1 site (Málaga) |
| Trial ID | NCT04547634 on ClinicalTrials.gov |
What this trial studies
This study aims to evaluate the feasibility and effectiveness of an online Therapeutic Exercise and Education Program (TEEP) for cancer patients and survivors. It focuses on improving physical function, quality of life, and managing symptoms like cancer-related fatigue, especially in the context of challenges posed by the COVID-19 pandemic. The program is designed to be accessible remotely, allowing patients to participate safely from home while receiving guidance on exercise and nutrition. The study will assess attendance, exercise prescription adherence, and changes in weight and physical function among participants.
Who should consider this trial
Good fit: Ideal candidates include metastatic breast cancer patients, gynecological cancer patients, or breast cancer survivors currently undergoing adjuvant treatment.
Not a fit: Patients who are technophobic or have significant anxiety about being at home may not benefit from this program.
Why it matters
Potential benefit: If successful, this program could enhance the recovery and quality of life for cancer patients and survivors by providing accessible exercise and education.
How similar studies have performed: Other studies have shown positive outcomes with similar online exercise interventions for cancer patients, indicating potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Metastatic breast patient, gynecological cancer patient, or breast cancer survivor under adjuvant treatment after surgical intervention. * Having given informed consent to participate voluntarily in the program and to be in contact via telematics (email or messaging platform). * Have a good internet connection * Be accompanied by an adult on the day of assessment. * Availability to access the computer on during the intervention. Exclusion Criteria: * Technophobia * Domatophobia or self-report of adversity to be at home. * Lack of logistical requirements (Internet and lack of skill in its use).
Where this trial is running
Málaga
- Antonio Cuesta Vargas — Málaga, Spain (Recruiting)
Study contacts
- Study coordinator: Antonio I Vargas, PhD, PT
- Email: acuesta@uma.es
- Phone: 0034951952852
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.