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Clinical Trials in Spain / NCT07572760
Recruiting Not applicable

Low to Moderate Load Power Training for Men With Metastatic Prostate Cancer.

NCT07572760 · tracked via the Priya Life Science Spain tracker
Phase
Not applicable
Started
2024-04-10
Last updated
2026-05-07

Condition(s) studied

Prostatic Neoplasms

Investigational drug(s) / intervention(s)

Power training group

Power training group: The intervention consists of a supervised power-oriented resistance training program for older men with prostate cancer undergoing androgen deprivation therapy (ADT). Participants will complete 2 sessions per week over 24 weeks. Training focuses on improving muscle power through exercises performed at moderate intensity (40-50% 1RM), emphasizing a fast concentric phase and controlled eccentric phase. Multi-joint functional exercises targeting major muscle groups are included to enhance strength, balance, and daily functional performance. Training volume is low-to-moderate, and participants do not train to muscular failure, allowing maintenance of movement velocity and reducing fatigue. Adequate rest periods are provided between sets. The program is adapted to the clinical characteristics of the population, minimizing mechanical stress while promoting neuromuscular improvements. It is designed to be safe, feasible, and well-tolerated, with the aim of improving functional capacity.

Study summary

The goal of this clinical trial is to learn if a low to moderate load power training program is feasible and effective for improving fitness and quality of life of people with prostate cancer under androgen suppression therapy and bone or lymph node metastasis. The main questions it aims to answer are:

* Does a low to moderate load power training program improve quality of life in people with metastatic prostate cancer under androgen deprivation therapy?
* Does a low to moderate load power training program improve power, strength, endurance, and balance in people with metastatic prostate cancer under androgen deprivation therapy?

Researchers will compare the exercise program with routine care to see if power training works to improve common physical side effects of androgen suppression therapy in patients with metastatic prostate cancer.

Participants will:

* Participate in a supervised exercise program twice a week for 6 months or maintain routine care.
* Perform fitness tests and questionnaires about quality of life and mental health.
* Those who take part in the exercise program will also perform semi-structured in-depth interviews after the end of the program.

Eligibility

Sex
MALE
Min age
50 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Histopathologically confirmed diagnosis of prostate adenocarcinoma. • Metastatic hormone-sensitive prostate cancer (mHSPC), defined as: * Presence of metastases at initial diagnosis (synchronous mHSPC), or * Development of metastatic disease following prior treatment with curative intent (surgery and/or radiotherapy) (metachronous mHSPC). * Evidence of progression to castration-resistant prostate cancer (CRPC). * Ongoing treatment with a doublet regimen consisting of standard androgen deprivation therapy (ADT) in combination with an androgen receptor signaling inhibitor (ARSI), initiated prior to study enrollment. * Receipt of bone-protective therapy, including calcium and vitamin D supplementation in combination with bisphosphonates. * Presence of metastatic involvement limited to bone and/or lymph nodes. * Functionally independent in activities of daily living. Exclusion Criteria: * Evidence of visceral metastatic disease. * Current or prior treatment with a triplet regimen that includes chemotherapy. * History of pathological fracture.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
University of Alicante San Vicent del Raspeig Alicante Recruiting

More University of Alicante trials in Spain

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07572760 on ClinicalTrials.gov ↗ ← All trials in Spain