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Effect Size and Evaluation of a Physical Group Training Intervention in the Integrative Care of Oncology Patients – A Pilot Study

Effect Size and Evaluation of a Physical Group Training Intervention in the Integrative Care of Oncology Patients – A Pilot Study - EFFEKTIV

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00037644
Enrollment
24
Registered
2026-02-17
Start date
2025-12-16
Completion date
Unknown
Last updated
2026-03-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Oncological and hemato-oncological patients

Interventions

Group 1: Oncological patients participating in weekly supervised group training sessions Group 2: Oncological patients who do not want to participate in a weekly group training.

Sponsors

LMU Klinikum, Medizinische Klinik und Poliklinik III
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Medical clearance for exercise and training eligibility (in cooperation with Med I, LMU Center for Sports Medicine) Ability to give informed consent at the time of study enrollment and signed informed consent form Legal adulthood at the time of study enrollment (minimum 18 years old)

Exclusion criteria

Exclusion criteria: - Lack of capacity to consent or being underage at the time of study enrollment - Medical or psychological condition which, in the opinion of the study team, prevents the patient from participating in the study or from providing a legally valid signed informed consent - Pregnancy - Existing contraindications to exercise therapy interventions, in particular: -Clinically manifest heart failure (NYHA class III-IV) - Therapy-resistant arterial hypertension grade III-IV - Respiratory insufficiency, severe COPD greater than grade III - Therapy-resistant thrombocytopenia <10,000/µl, or coagulation disorders with clinically significant increased bleeding risk - Unstable coronary syndrome or unstable cardiac arrhythmias -Uncontrolled cerebral epilepsy - Implanted pacemaker or defibrillator

Design outcomes

Primary

MeasureTime frame
The primary endpoint is the feasibility and training adherence of a structured exercise program.

Secondary

MeasureTime frame
Secondary endpoints: - Assessment of training commitment and possible positive and negative factors influencing adherence. - Change in physical performance. - Change in quality of life. - Change in nutritional status and body composition.

Countries

Germany

Contacts

Public ContactAnouk Erb

LMU Klinikum, Medizinische Klinik und Poliklinik III

anouk.erb@med.uni-muechen.de+498944000

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Mar 14, 2026