Comparing resistance training methods for breast cancer survivors
Effects of Different Methods of Prescription and Monitoring of Resistance Training Intensity on Muscle Strength, Body Composition, and Psychological Well-being in Survivors of Breast Cancer
This study tests different ways of doing resistance training to see which helps breast cancer survivors get stronger, feel better, and improve their overall health.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 18 Years and up |
| Sex | Female |
| Sponsor | Universidad de Almeria Academic / other |
| Drugs / interventions | chemotherapy |
| Locations | 1 site (Almería, Almeria) |
| Trial ID | NCT06940310 on ClinicalTrials.gov |
What this trial studies
This clinical trial aims to evaluate the effects of three different resistance training intensity prescription and monitoring methods on muscle strength, body composition, and overall well-being in breast cancer survivors. Participants will engage in resistance training with varying approaches: daily load-velocity adjustments, initial one-repetition maximum (1RM) estimations, and traditional 1RM-based prescriptions. The study seeks to address common issues faced by breast cancer survivors, such as muscle weakness, fatigue, and psychological distress, by optimizing resistance training protocols. The findings will help develop evidence-based exercise guidelines tailored for this population.
Who should consider this trial
Good fit: Ideal candidates are breast cancer survivors over 18 years old who have completed their cancer treatments within the last 10 years.
Not a fit: Patients with metastatic breast cancer or those planning reconstructive surgery within three months may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance the quality of life and physical health of breast cancer survivors through optimized exercise interventions.
How similar studies have performed: Other studies have shown positive outcomes with resistance training in cancer survivors, but this specific approach to intensity prescription is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * To be \>18 years old. * To have a breast cancer diagnosis. * To have finished chemotherapy, radiotherapy and/or surgery up to 10 years prior to the beginning of the study. Exclusion Criteria: * To present metastatic breast cancer. * To have a planned surgery for breast reconstruction within three months after the start of the study. * To present any absolute contraindication for exercising.
Where this trial is running
Almería, Almeria
- University of Almeria — Almería, Almeria, Spain (Recruiting)
Study contacts
- Principal investigator: Alberto Soriano-Maldonado — Universidad de Almeria
- Study coordinator: Alberto Soriano-Maldonado
- Email: asoriano@ual.es
- Phone: 950015550
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.