IMPLEMENT - Model Project for Quality-assured Exercise Therapy for Cancer Patients

NCT06496711 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 600

Last updated 2024-08-23

No results posted yet for this study

Summary

IMPLEMENT aims to develop, test and establish a sustainable access structure for quality-assured oncological exercise therapy (qOET) in Germany as a model within the funding period of three years. This will be done in three phases:

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.

Conditions

Interventions

OTHER

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.

Sponsors & Collaborators

  • Leibniz Institute for Prevention Research and Epidemiology - BIPS GmbH

    collaborator OTHER
  • University of Regensburg

    collaborator OTHER
  • Ludwig-Maximilians - University of Munich

    collaborator OTHER
  • Technical University of Munich

    collaborator OTHER
  • Martin-Luther-Universität Halle-Wittenberg

    collaborator OTHER
  • University Hospital Schleswig-Holstein

    collaborator OTHER
  • Universitätsklinikum Hamburg-Eppendorf

    collaborator OTHER
  • University Hospital, Essen

    collaborator OTHER
  • University of Cologne

    lead OTHER

Principal Investigators

  • Hajo Zeeb, Prof. Dr. · Leibniz Institute for Prevention Research and Epidemiology - BIPS GmbH

  • Freerk Baumann, Prof. Dr. · University of Cologne

  • Michael Leitzmann, Prof.Dr.Dr. · University of Regensburg

Study Design

Allocation
NA
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
5 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-09-01
Primary Completion
2025-11-30
Completion
2026-02-28

Countries

  • Germany

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06496711 on ClinicalTrials.gov