Optimizing Patient Information Material for a New Psycho-Oncological Care Program Using a Participatory Health Research Approach in Germany.

cancer optimization process participation participatory health research patient engagement patient information material psycho-oncological support quality assessment

Journal

International journal of environmental research and public health
ISSN: 1660-4601
Titre abrégé: Int J Environ Res Public Health
Pays: Switzerland
ID NLM: 101238455

Informations de publication

Date de publication:
28 01 2022
Historique:
received: 17 12 2021
revised: 24 01 2022
accepted: 25 01 2022
entrez: 15 2 2022
pubmed: 16 2 2022
medline: 1 3 2022
Statut: epublish

Résumé

High-quality patient information material (PIM) is essential for patients´ informed decision-making, and its quality may influence a care program's acceptance. In the new psycho-oncological care program, isPO, the initial PIM was developed top-down and required optimization. In this paper, we report on the process and experiences of optimizing PIM's quality bottom-up by applying a Participatory Health Research (PHR) approach. Cancer-patient representatives of the national peer-support group contributed as co-researchers as part of the optimization team. A mixed-methods design was chosen. First, the quality of the initially utilized PIM was assessed with the newly designed user-friendly instrument UPIM-Check. Next, three Participatory Action Research loops were conducted, including cancers survivors and isPO service providers. The initial isPO PIM's were assed to be of low quality, limited usability and incomplete. Bottom-up generated optimization suggestions led to the improvement of two initially used PIMs (leaflet, patient information folder) and the design of two new PIMs (poster, study information overview). The optimized PIM facilitates isPO service providers' care provision and helps newly diagnosed cancer patients in understanding and accepting the new program. PIM optimization benefited from applying PHR. The patient representatives' contribution and active patient engagement were central for quality assessment and designing needs-driven, mature and complete PIM.

Identifiants

pubmed: 35162540
pii: ijerph19031518
doi: 10.3390/ijerph19031518
pmc: PMC8835450
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Theresia Krieger (T)

Institute of Medical Sociology, Health Services Research and Rehabilitation Science (IMVR), University of Cologne, 50933 Cologne, Germany.

Sandra Salm (S)

Institute of Medical Sociology, Health Services Research and Rehabilitation Science (IMVR), University of Cologne, 50933 Cologne, Germany.

Antje Dresen (A)

Institute of Medical Sociology, Health Services Research and Rehabilitation Science (IMVR), University of Cologne, 50933 Cologne, Germany.

Anna Arning (A)

German Cancer Society North-Rhine Westphalia (KG-NRW), 40221 Düsseldorf, Germany.

Kathrin Schwickerath (K)

German Cancer Society North-Rhine Westphalia (KG-NRW), 40221 Düsseldorf, Germany.

Andrea Göttel (A)

German Cancer Society North-Rhine Westphalia (KG-NRW), 40221 Düsseldorf, Germany.

Stefanie Houwaart (S)

House of the Cancer Patient Support Associations of Germany (HKSH-BV), 53111 Bonn, Germany.

Holger Pfaff (H)

Institute of Medical Sociology, Health Services Research and Rehabilitation Science (IMVR), University of Cologne, 50933 Cologne, Germany.

Natalia Cecon (N)

Institute of Medical Sociology, Health Services Research and Rehabilitation Science (IMVR), University of Cologne, 50933 Cologne, Germany.

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