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RECRUITINGINTERVENTIONAL

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

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

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 May Be Eligible (Plain English)

Who May Qualify: - 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 Who Should NOT Join This Trial: - 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 Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
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

Treatments Being Tested

BEHAVIORAL

Prehabilitation

Targeted exercise and psychooncological program

BEHAVIORAL

standard of care

Clinical routine as applied in Germany

Locations (1)

University hospital Münster
Münster, North Rhine-Westphalia, Germany