Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT07464457

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

Led by Priv.-Doz. Dr. med. Philipp Lenz · Updated on 2026-03-11

125

Participants Needed

1

Research Sites

187 weeks

Total Duration

On this page

AI-Summary

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

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with solid tumors, focusing on breast cancer
  • Planned curative-intent surgery or radiotherapy
  • Aged between 18 and 65 years
  • ECOG performance status 0 to 2
  • Sufficient language skills to understand questionnaires and training instructions
Not Eligible

You will not qualify if you...

  • Severe cardiac or lung diseases preventing participation
  • Medical reasons that contraindicate physical activity
  • Unable to provide informed consent
  • Pregnancy or breastfeeding
  • Acute infections or fever
  • Participation in another clinical intervention study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University hospital Münster

Münster, North Rhine-Westphalia, Germany, 48149

Actively Recruiting

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Research Team

M

Mira Meyer-Ács

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

SEQUENTIAL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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