Prehabilitation: Targeted exercise and psychooncological program
standard of care: Clinical routine as applied in Germany
Study summary
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
Eligibility
Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
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
Primary outcome measure(s)
Physical performance using the 6-Minute Walk Test — From enrollment to 14 - 28 days after ablative intervention Physical performance at post-intervention (14-28 days after the ablative intervention), assessed using the 6-Minute Walk Test.
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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