SPORT-MUResistance Training Program for Prostate Cancer Patients on Androgen Deprivation Therapy
Exercise Intervention Protocol
+ SPoRT-Control Intervention
Urogenital Diseases+7
+ Genital Diseases
+ Genital Diseases, Male
Treatment Study
Summary
Study start date: November 15, 2025
Actual date on which the first participant was enrolled.This study is exploring the impact of a structured exercise program on men with prostate cancer who are undergoing a common treatment called androgen deprivation therapy (ADT). Prostate cancer patients often experience side effects from ADT that affect their physical and mental well-being. This research aims to find out if a 24-week exercise program can help improve these patients' physical strength, daily functioning, and overall mood. By comparing two different types of exercise routines, the study hopes to discover which one is more beneficial, potentially leading to better care and quality of life for these patients. Participants in this study are randomly assigned to one of two groups. One group follows a supervised resistance training program, while the other does exercises at home with guidance given during the first session and regular phone check-ins. Evaluations occur at the start, halfway through, and at the end of the 24 weeks to see how the exercise affects physical, functional, and emotional health. This setup allows researchers to measure both the immediate and lasting effects of the exercise programs, offering insights into which approach might be more effective for men undergoing ADT.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.60 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Male
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
Active ComparatorGroup II
ExperimentalStudy Objectives
Primary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location