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NCT07162987Recruiting

Prehabilitation to Patients With Prostate Cancer

Prehabilitation to Patients With Prostate Cancer, Who Are About to Receive Androgen Deprivation Therapy and Radiation Therapy

Source: ClinicalTrials.gov · Last updated 9 Sept 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The goal of this feasibility study is to test a newly developed, multicomponent prehabilitation intervention to patients with prostate cancer, to improve their resilience to treatment side-effects. The main questions it aims to answer are: * Are patients and their close relatives willing to take part in prehabilitation? * What is the acceptability and feasibility of the prehabilitation intervention, seen from the perspectives of patients, their close relatives, and healthcare professionals? * Are the planned data collection methods feasible, and are there indications of a clinical effect? Participants will: * Take part in 12 weeks of physical exercise training * Attend a 4-day residential prehabilitation intervention, where they receive education and do exercises. After 12 weeks, it is possible to take part in a voluntary follow-up session. * Patients will respond to questionnaires about their health, symptoms, and quality of life. Patients and their close relatives will attend a group interview. Patients will also complete an exercise diary and brief physical tests

Status (registry)
Recruiting
Study type
Interventional
Enrollment
20 (estimated)
First submitted
30 Jul 2025
Start date
4 Aug 2025
Primary completion date
Nov 2026
Lead sponsor
Odense University Hospital
NCT number
NCT07162987

What you commit to

  • Study type: Interventional
  • Planned participants: 20
  • From 4 Aug 2025 to the primary completion date, Nov 2026
  • 3 sites 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.

Other

  • Persons who do not fulfil the inclusion criteria will be excluded

Who the study is looking for

  • Diagnosed with prostate cancer
  • min 18 years old
  • Treatment: Androgen deprivation therapy and raditation therapy
  • Resident in Vejle Municipality or Esbjerg Municipality
  • Can take part in residential prehabiliation in week 43 or 50, 2025, as well as physical exsercise training in the municipality
  • Willing to take part in a research study
  • Suited to take part in group sessions
  • Be able to read and be understood in Danish
  • Be responsible for own personal hygiene and medications at the 4-day residential stay

Age in the registry: 18 years to - · Sex: Male · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (3)

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

SiteCityCountrySite status
Esbjerg Hospital
Coordinator of this site? Confirm its status
EsbjergDenmarkRecruiting
REHPA, the Danish Knowledge Centre for Rehabilitation and Palliative Care
Coordinator of this site? Confirm its status
NyborgDenmarkRecruiting
Vejle Hospital
Coordinator of this site? Confirm its status
VejleDenmarkRecruiting

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