Effects of Neoadjuvant Prehabilitation on Post-Interventional Physical and Psychological Outcomes in Oncology Patients With Solid Tumors
Recruiting · NCT07464457 · Interventional (participants receive a specific treatment)
View the official record on ClinicalTrials.gov →Interventions studied
Prehabilitationstandard of care
What this trial is about
The goal of NEOPRO-SIT is to establish and evaluate a neoadjuvant prehabilitation program comprised of targeted exercise therapy and structured psycho-oncological support in patients with solid tumors. The main question is: Will targeted exercise therapy and structured psycho-oncological support increase both physical and psychological capacity as well of quality of life compared to standard of care in a prehabilitation setting? Researchers will: compare a prehabilitation program to standard of care Participants will: receive either standard or care or a comprehensive prehabilitation program
Who can take part
Age range
18 Years to 65 Years
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
Inclusion criteria
- Patients with solid tumors (focus on breastcancer)
- Curative-intent multimodal treatment concept with local surgical or radiotherapeutic ablation
- Working age and \> 18 years
- ECOG 0-2
- Sufficient language skills to understand questionnaires/training instructions
Exclusion criteria
- Severe cardiac or pulmonary comorbidities that do not allow participation in the program
- Medical contraindications for physical activity
- Lack of patient capacity to consent
- Pregnancy/breastfeeding
- Acute infections/fever
- Participation in another clinical intervention study
Where it is running
1 location listed.
- University hospital Münster - Münster, North Rhine-Westphalia, Germany