Actively Recruiting

Phase Not Applicable
Age: 50Years +
MALE
NCT07572760

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

Led by University of Alicante · Updated on 2026-05-07

66

Participants Needed

1

Research Sites

139 weeks

Total Duration

On this page

Sponsors

U

University of Alicante

Lead Sponsor

H

Hospital General Universitario Dr. Balmis de Alicante

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 50Years +
MALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Histopathologically confirmed diagnosis of prostate adenocarcinoma.
  • Metastatic hormone-sensitive prostate cancer (mHSPC), either present at initial diagnosis or developed after prior treatment with surgery and/or radiotherapy.
  • Evidence of progression to castration-resistant prostate cancer (CRPC).
  • Currently receiving a doublet treatment of standard androgen deprivation therapy combined with an androgen receptor signaling inhibitor, started before study enrollment.
  • Receiving bone-protective therapy including calcium, vitamin D, and bisphosphonates.
  • Metastatic disease limited to bone and/or lymph nodes.
  • Functionally independent in daily activities.
Not Eligible

You will not qualify if you...

  • Presence of visceral metastatic disease.
  • Current or past treatment with a triplet regimen that includes chemotherapy.
  • History of pathological fracture.

AI-Screening

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Trial Site Locations

Total: 1 location

1

University of Alicante

San Vicent del Raspeig, Alicante, Spain, 03690

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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