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Social Prescriptions and Micro-Learning to Improve Care for Cancer Patients and Their Support Persons

Sponsor: University of Regensburg • ClinicalTrials.gov ID: NCT07788729

Registry updated: 2026-08-26

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Description

Optimal patient-centered care is often not being delivered to cancer patients, especially to vulnerable populations like those living in underserved rural areas. This body of work will develop and pilot test a multicomponent intervention approach designed to improve the care and outcomes of cancer patients and their support persons (SPs) during and following their therapeutic journey. The intervention will involve the provision of social prescriptions and web-based micro-learning modules, as well as stepwise care based on ongoing monitoring of symptom burden and health. This project uses the strengths of innovative, individually tailored communication strategies and a comprehensive low-cost approach that are likely to support fair and equal patient access to optimal care beyond the funding period. By using a patient-driven approach in an interdisciplinary setting, it is anticipated that the intervention will improve the health outcomes of various patient populations, especially those living in rural areas. To achieve this, a methodologically robust mixed-methods approach and an effectiveness-implementation hybrid design will be employed to move effective strategies towards implementation into clinical practice. A number of standardized patient-reported outcome and experience measures will be used, including quality of life and knowledge of health and care. As a result of this research, an implementation toolbox will be developed that could be used by clinicians working in different healthcare settings and services, both nationally and internationally, to help provide highest quality cancer care.

Interventions

PRISMA-interventions (Other)
A multicomponent intervention including social prescriptions, web-based micro-learning modules, and stepwise care based on symptom monitoring.

Eligibility criteria

Inclusion Criteria for patients: * aged at least 18 years * primary diagnosis of early-stage or advanced-stage lung cancer, colorectal cancer, hematological neoplasm or malignant melanoma within the past 12 months * expected survival of at least 18 months * sufficient German language proficiency to complete questionnaires and interviews * attendance at the medical oncology units of participating hospitals * provision of written informed consent * ECOG Performance Status 0-2 * ability to name an eligible SP. Inclusion criteria for Support Persons: * being nominated by the patient as someone who provides support, encouragement or assistance in coping with their cancer * aged at least 18 years * proficiency in German * provision of written informed consent. Exclusion Criteria: Inability to * provide informed consent * independently complete interviews and/or questionnaires due to impaired speech, vigilance, or comprehension.

Conditions

Cancer Lung Cancer Colorectal Cancer Hematological Cancer Malignant Melanoma

Locations

University Hospital Augsburg — Augsburg, Bavaria, Germany
University Hospital Erlangen — Erlangen, Bavaria, Germany
University Hospital Regensburg — Regensburg, Bavaria, Germany
University Regensburg — Regensburg, Bavaria, Germany
University Hospital Würzburg — Würzburg, Bavaria, Germany
Faculty of Law, Business & Economics, Inst. for Healthcare Management & Health Sciences — Bayreuth, Germany
Charité - University Medicine Berlin — Berlin, Germany
University Hospital Köln — Cologne, Germany

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Official Source

Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

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