Actively Recruiting
Training for Men Undergoing Androgen Deprivation Therapy.
Led by The Swedish School of Sport and Health Sciences · Updated on 2024-06-10
60
Participants Needed
1
Research Sites
242 weeks
Total Duration
On this page
Sponsors
T
The Swedish School of Sport and Health Sciences
Lead Sponsor
N
Norwegian School of Sport Sciences
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this clinical trial is to evaluate the effects of a newly developed training concept on men with prostate cancer undergoing androgen deprivation therapy (ADT). The main questions it aims to answer are: * How feasible and safe is the new training concept? * How efficient is the training concept to counteract side effects caused by ADT? Researchers will compare the new training concept with usual care to evaluate how efficient the training concept is to counteract the ADT-related side effects. Participants in the intervention group will perform the new training concept twice weekly for 12 weeks. Participants in the control group will only receive usual care. All participants will visit the laboratory at baseline and after 6 and 12 weeks to measure the primary and secondary outcomes.
CONDITIONS
Official Title
Training for Men Undergoing Androgen Deprivation Therapy.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Signed informed consent
- Histologically confirmed localized or locally advanced prostate cancer
- Planned radiotherapy combined with androgen deprivation therapy for at least six months with curative intent
- No known metastasis
- Men aged 50 to 80 years
You will not qualify if you...
- Very high risk localized prostate cancer planned for radiotherapy and ADT plus abiraterone and cortisone
- Localized prostate cancer planned for radiotherapy without ADT
- Ongoing or previous treatment with androgen deprivation therapy or other hormonal treatments
- Any contraindications to physical testing or exercise according to ACSM guidelines
- Unable to comply with study procedures
AI-Screening
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Trial Site Locations
Total: 1 location
1
Swedish School of Sport and Health Sciences
Stockholm, Sweden, 11486
Actively Recruiting
Research Team
N
Niklas Psilander, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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