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NCT06449664Recruiting

Training for Men Undergoing Androgen Deprivation Therapy.

ADT-Train - A New Training Concept for Men With Prostate Cancer Receiving Androgen Deprivation Therapy.

Source: ClinicalTrials.gov · Last updated 10 Jun 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
60 (estimated)
First submitted
4 Apr 2024
Start date
1 May 2024
Primary completion date
Dec 2026
Lead sponsor
The Swedish School of Sport and Health Sciences
NCT number
NCT06449664

What you commit to

  • Study type: Interventional
  • Planned participants: 60
  • From 1 May 2024 to the primary completion date, Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • on-going or previously treated with ADT or other hormonal treatments

Other illness

  • very high risk localised prostate cancer planned for radiotherapy and ADT plus abiraterone and cortisone
  • localized prostate cancer planned for radiotherapy without ADT

Other

  • have any contraindications to physical testing/exercise as per the ACSM guidelines
  • unable to comply with study procedures

Who the study is looking for

  • 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.

Age in the registry: 50 years to 80 years · Sex: Male · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Swedish School of Sport and Health Sciences
Coordinator of this site? Confirm its status
StockholmSwedenRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.