RecruitingNot ApplicableNCT07464457

Effects of Neoadjuvant Prehabilitation on Post-Interventional Physical and Psychological Outcomes in Oncology Patients With Solid Tumors

Effects of Neoadjuvant Prehabilitation on Post-Interventional Physical and Psychological Outcomes in Oncology Patients With Solid Tumors: A Prospective, Two-arm, Controlled, Monocentric Interventional Study


Sponsor

Priv.-Doz. Dr. med. Philipp Lenz

Enrollment

125 participants

Start Date

Mar 1, 2026

Study Type

INTERVENTIONAL

Conditions

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

Min Age: 18 YearsMax Age: 65 Years

Plain Language Summary

Simplified for easier understanding

This study is testing whether a structured exercise and preparation program before cancer treatment (called prehabilitation) helps patients with solid tumors recover better physically and mentally after surgery or radiation. The focus is especially on breast cancer patients. **You may be eligible if...** - You have been diagnosed with a solid tumor (especially breast cancer) - You are receiving treatment with curative intent (surgery or radiation to eliminate the cancer) - You are working-age and over 18 years old - You are able to understand questionnaires and exercise instructions - You have an ECOG performance status of 0–2 (able to carry out daily activities) **You may NOT be eligible if...** - You have serious heart or lung conditions that prevent exercise - You have a medical contraindication to physical activity - You are pregnant or breastfeeding - You are currently participating in another clinical intervention study Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

BEHAVIORALPrehabilitation

Targeted exercise and psychooncological program

BEHAVIORALstandard of care

Clinical routine as applied in Germany


Locations(1)

University hospital Münster

Münster, North Rhine-Westphalia, Germany

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NCT07464457


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