Actively Recruiting
Prehabilitation for Patients Diagnosed With Blood Cancer and Treated With Allogeneic Hematopoietic Stem Cell Transplantation - a National Randomized Controlled Trial
Led by Rigshospitalet, Denmark · Updated on 2026-01-29
110
Participants Needed
1
Research Sites
247 weeks
Total Duration
On this page
Sponsors
R
Rigshospitalet, Denmark
Lead Sponsor
A
Aarhus University Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are studying adults diagnosed with blood cancer who are scheduled to receive allogeneic hematopoietic stem cell transplantation, an intensive treatment associated with long hospital stays and muscle weakness. The trial aims to evaluate whether an individualized prehabilitation program combined with usual care improves health-related quality of life compared to usual care alone. This trial is a national randomized controlled study assessing the effects of exercise and nutrition before transplantation, addressing common challenges like muscle dysfunction and fatigue in this population. Participants are randomly assigned to one of two groups. The usual care group receives standard treatment including physical and occupational therapy during hospitalization and possible rehabilitation referrals afterward. The experimental group receives usual care plus supervised, personalized resistance training three times per week and optimized nutritional support with tailored dietary counseling and supplements. The intervention starts at least four weeks before transplantation. During the study, participants undergo assessments from enrollment to 90 days after transplantation. Researchers measure health-related quality of life using a cancer-specific questionnaire, the duration of hospitalization, muscle mass and strength, including hand grip and lower limb function. The study includes muscle function tests and tracks outcomes to understand the intervention's impact on recovery and well-being after transplantation.
CONDITIONS
Brief Title
Prehabilitation for Patients Diagnosed With Blood Cancer and Treated With Al-logeneic Hematopoietic Stem Cell Transplantation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult patients over 18 years old
- Scheduled for allogeneic hematopoietic stem cell transplantation at least four weeks before transplantation date
You will not qualify if you...
- Pregnancy
- Physical or mental disabilities preventing muscle function testing
- Inability to read and understand Danish or English
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - From enrollment to 90 days post-transplantation
Participants receive either usual care or usual care plus a supervised, individually tailored resistance training and optimized nutritional support before their transplantation.
Weekly visits for up to 12 weeks
Trial Site Locations
Total: 1 location
1
Copenhagen University Hospital - Rigshospitalet
Copenhagen, Denmark, Denmark, 2100
Actively Recruiting
Research Team
J
Jan Christensen, PhD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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