IMPLEMENT - Model Project for Quality-assured Exercise Therapy for Cancer Patients
NCT ID: NCT06496711
Last Updated: 2024-08-23
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
600 participants
INTERVENTIONAL
2023-09-01
2026-02-28
Brief Summary
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Phase 1: In the first step, a characterization of the existing implementation structures and the existing barriers and needs as well as the establishment of the cooperation with the most important actors in the care system will take place.
Phase 2: In the subsequent implementation process, concrete measures are practically implemented in subprojects for specific target groups (children/adolescents, adults) and specific regions (rural, urban) as well as the digital solutions and interface management. With the help of a mixed-methods design, the barriers and facilitating factors of the implementation of area-wide qSBT will be investigated during the project and fed into a "learning system" for adaptation and improvement.
Phase 3: The success of the measures to increase patient participation in qOET and the development of the structures as well as the barrier and facilitating factors for an effective implementation will be addressed in a before-after comparison through evaluation steps and an economic accompanying evaluation will be carried out.
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Detailed Description
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Risks to achieving the objectives include the willingness of patients to participate in qOET and the willingness of doctors, therapists and other people working in oncological care to implement the interventions and to expand and adapt their professional activities accordingly. To address these challenges, a mixed-methods approach is used to identify barriers and facilitators. A mixed-methods approach enables a theoretical understanding of the implementation process and provides a more comprehensive picture of the factors relevant to successful implementation than qualitative or exclusively quantitative methods alone.
Conditions
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Study Design
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NA
SINGLE_GROUP
SUPPORTIVE_CARE
NONE
Study Groups
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Cancer Patients and Parents of Cancer Patients
Children: Age 5-12 years Parents of children with cancer Teenager: Age 13-17 years Parents of teenager with cancer AYAs: Adolescence and young adults: Age 18-39 years Adults: \> 40 years
Cancer Patients; Institutions and their employees in the treatment and/or counseling of cancer patients
The study population will be surveyed at 3 yearly measurement time points by means of questionnaires and interviews on attitudes, barrier and support factors for participation in exercise therapy.
Interventions
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Cancer Patients; Institutions and their employees in the treatment and/or counseling of cancer patients
The study population will be surveyed at 3 yearly measurement time points by means of questionnaires and interviews on attitudes, barrier and support factors for participation in exercise therapy.
Eligibility Criteria
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Inclusion Criteria
* Healthcare providers (e.g. Medical Doctors, physiotherapists, nurses, psychologists) involved in the treatment and/or counseling of cancer patients, including aftercare.
Exclusion Criteria
5 Years
ALL
No
Sponsors
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Leibniz Institute for Prevention Research and Epidemiology - BIPS GmbH
OTHER
University of Regensburg
OTHER
Ludwig-Maximilians - University of Munich
OTHER
Technical University of Munich
OTHER
Martin-Luther-Universität Halle-Wittenberg
OTHER
University Hospital Schleswig-Holstein
OTHER
Universitätsklinikum Hamburg-Eppendorf
OTHER
University Hospital, Essen
OTHER
University of Cologne
OTHER
Responsible Party
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Freerk Baumann; Prof. Dr.
Prof. Dr. Freerk Baumann
Principal Investigators
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Freerk Baumann, Prof. Dr.
Role: PRINCIPAL_INVESTIGATOR
University of Cologne
Michael Leitzmann, Prof.Dr.Dr.
Role: PRINCIPAL_INVESTIGATOR
University of Regensburg
Hajo Zeeb, Prof. Dr.
Role: PRINCIPAL_INVESTIGATOR
Leibniz Institute for Prevention Research and Epidemiology - BIPS GmbH
Locations
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University Hospital Cologne
Cologne, , Germany
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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UCologne 70114696
Identifier Type: -
Identifier Source: org_study_id
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