Actively Recruiting
Multi-professional Care Pathway and Network for the Promotion of Needs-oriented, Resident-oriented Exercise Therapy for Oncological Patients
Led by University Hospital Heidelberg · Updated on 2025-02-03
2500
Participants Needed
7
Research Sites
200 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
MOVE-ONKO is developing and implementing a guideline-based, multi-professional care pathway for the promotion and therapy of exercise for cancer patients. This pathway intended to serve as an interface between oncological care and existing or developing exercise therapy services in the local area of the participating hospitals. Needs- and side-effect-oriented care pathways are intended to give as many patients as possible access to quality-assured exercise therapy services close to home and thus to the supportive potential of exercise. The new care pathway will be develop in year 1 (phase 1) and will be established at 7 Comprehensive Cancer Centers (CCCs) in 3 model regions Heidelberg-Frankfurt-Mainz, Dresden-Berlin and Freiburg-Tübingen (phase 2) in Germany, as well as adapted accordingly in organ cancer centers and with established oncological care providers (phase 3 - Outreach). The aim is to ensure that exercise promotion and therapy can be integrated into standard care as comprehensively and sustainably as possible. The implementation project will be evaluated according to the achievement of implementation and intervention goals. The implementation goals are utilization (reach) and actual implementation. Factors for successful implementation will be identified and incorporated into the procedure in phase 3 (outreach). Intervention goals are mapped at provider and patient level in both phases. They include improving physical functioning, increasing physical activity behavior, improving exercise-related health literacy, increasing motivation to exercise and increasing patient participation. For this purpose, patients with a cancer disease undergoing acute therapy aged 18 and over who are cared for in participating centers are surveyed four times over a period of 24 weeks using standardized questionnaires (baseline (t0) before the intervention, follow-up after 4 (t1), 12 (t2) and 24 (t3) weeks). In addition, the participating managers and service providers of the centers in phase 2 (implementation phase) and phase 3 (outreach phase) will be surveyed using standardized questionnaires and in-depth interviews. The longitudinal evaluation design enables an analysis of the changes in care structures and processes, the success of implementation and the experiences and outcomes of patients
CONDITIONS
Official Title
Multi-professional Care Pathway and Network for the Promotion of Needs-oriented, Resident-oriented Exercise Therapy for Oncological Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Cancer patients currently undergoing chemotherapy, immunotherapy, or radiotherapy
- Patients experiencing symptoms or side effects that exercise can help treat, such as fatigue, or who are interested in exercise oncology counseling
- Care providers involved in the implementation process
You will not qualify if you...
- Insufficient German language skills
- Care providers employed for less than 6 months
AI-Screening
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Trial Site Locations
Total: 7 locations
1
Universitätsklinikum Freiburg
Freiburg im Breisgau, Baden-Wurttemberg, Germany, 79106
Actively Recruiting
2
Nationales Centrum für Tumorerkrankungen
Heidelberg, Baden-Wurttemberg, Germany, 69120
Actively Recruiting
3
Medizinische Klinik der Universitätsklinikum Tübingen
Tübingen, Baden-Wurttemberg, Germany, 72076
Actively Recruiting
4
Universitäres Centrum für Tumorekrankungen Frankfurt
Frankfurt am Main, Hesse, Germany, 60488
Actively Recruiting
5
Universitäres Centrum für Tumorerkrankungen Mainz
Mainz, Rhineland-Palatinate, Germany, 55131
Actively Recruiting
6
Nationales Centrum für Tumorerkrankungen Dresden (NCT/UCC)
Dresden, Saxony, Germany, 01307
Actively Recruiting
7
Charité - Universitätsmedizin Berlin
Berlin, State of Berlin, Germany, 10117
Actively Recruiting
Research Team
J
Joachim Wiskemann, Prof
CONTACT
J
Julia Albrecht, Dr
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
1
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