Training for Men Undergoing Androgen Deprivation Therapy.

Recruiting now · Not applicable

Conditions studied: Prostate Cancer

In brief

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.

Key facts

Study ID

NCT06449664

Run by

The Swedish School of Sport and Health Sciences

People needed

60

Starts

2024-05-01

Expected to finish

2028-12-20

Last updated by the study team

2024-06-10

Who can join

Age: 50 and older, up to 80. Sex: male. Healthy volunteers: not accepted.

You may qualify if…

• signed informed consent
• histologically confirmed localised or locally advanced prostate cancer
• planned radiotherapy in combination with ADT for at least six months (unfavorable intermediate risk and high-risk prostate cancer) with curative intent and with no known metastasis.

You may not qualify if…

• very high risk localised prostate cancer planned for radiotherapy and ADT plus abiraterone and cortisone
• localized prostate cancer planned for radiotherapy without ADT
• on-going or previously treated with ADT or other hormonal treatments
• have any contraindications to physical testing/exercise as per the ACSM guidelines
• unable to comply with study procedures

Where it is running

• Swedish School of Sport and Health Sciences — Stockholm, Sweden (enrolling)

Full record on ClinicalTrials.gov

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