Actively Recruiting
Prehabilitation to Patients With Prostate Cancer
Led by Odense University Hospital · Updated on 2025-09-09
20
Participants Needed
3
Research Sites
64 weeks
Total Duration
On this page
Sponsors
O
Odense University Hospital
Lead Sponsor
R
REHPA, The Danish Knowledge Centre for Rehabilitation and Palliative Care
Collaborating Sponsor
AI-Summary
What this Trial Is About
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
CONDITIONS
Official Title
Prehabilitation to Patients With Prostate Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosed with prostate cancer
- At least 18 years old
- Scheduled to receive androgen deprivation therapy and radiation therapy
- Resident in Vejle Municipality or Esbjerg Municipality
- Able to attend residential prehabilitation in week 43 or 50, 2025
- Able to participate in physical exercise training in the municipality
- Willing to take part in the research study
- Suitable for group sessions
- Able to read and understand Danish
- Responsible for own personal hygiene and medications during the 4-day residential stay
You will not qualify if you...
- Persons who do not meet the inclusion criteria will be excluded
AI-Screening
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Trial Site Locations
Total: 3 locations
1
Esbjerg Hospital
Esbjerg, Region Syddanmark, Denmark, 6700
Actively Recruiting
2
REHPA, the Danish Knowledge Centre for Rehabilitation and Palliative Care
Nyborg, Region Syddanmark, Denmark, 5800
Actively Recruiting
3
Vejle Hospital
Vejle, Region Syddanmark, Denmark, 7100
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
1
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