Journal Article DZNE-2026-00550

http://join2-wiki.gsi.de/foswiki/pub/Main/Artwork/join2_logo100x88.png
Identifying future research priorities for diversity-sensitive psychosocial interventions to manage dementia-related symptoms (GenderDem): protocol for a priority setting partnership study.

 ;  ;  ;  ;  ;  ;

2026
BMJ Publishing Group London

BMJ open 16(5), e111387 () [10.1136/bmjopen-2025-111387]

This record in other databases:    

Please use a persistent id in citations: doi:

Abstract: Gender, sex and ethnicity-sensitive approaches to psychosocial interventions for behavioural and psychological symptoms of dementia have been under-represented in the literature. Although the initial findings have revealed relevant differences with regard to sex, gender and ethnicity-sensitive approaches to those interventions. The GenderDem study aims to identify the top-10 research priorities in this context for future dementia care research.The methodological approach in GenderDem is based on the James Lind Alliance Guidebook and the concept of priority setting partnerships. In this participatory research approach, people living with dementia, their caregivers (and/or their loved ones) and healthcare professionals will be actively involved in the study. As members of a steering group, they act as coresearchers in the GenderDem study. We aim to recruit a diverse group of people for the steering group by considering different factors, eg, gender identity, sex, ethnicity and age. Future research priorities will be identified through two rounds of online surveys to collect and rank research topics from additional participants (eg, people with dementia, caregivers and/or loved ones and healthcare professionals). Additionally, a literature review and a workshop will be carried out in parallel to consider the current state of the research and to finalise the top-10 research priorities.An ethics application for conducting the two surveys and the workshop for this study has been approved by the German Society of Nursing Science (No. 25-029). Study participants will be informed in detail about the voluntary nature of their participation. Together with the coresearchers from the steering group, we will develop a dissemination plan that considers the different media consumption forms of the various groups. Additionally, we will disseminate our project results on an ongoing basis.

Keyword(s): Humans (MeSH) ; Dementia: therapy (MeSH) ; Dementia: psychology (MeSH) ; Caregivers: psychology (MeSH) ; Psychosocial Intervention (MeSH) ; Male (MeSH) ; Female (MeSH) ; Research Design (MeSH) ; Sex Factors (MeSH) ; Community-Based Participatory Research ; Dementia ; Psychosocial Intervention

Classification:

Contributing Institute(s):
  1. Implementation Science & Person-Centered Dementia Care (AG Roes)
Research Program(s):
  1. 353 - Clinical and Health Care Research (POF4-353) (POF4-353)

Database coverage:
Medline ; DOAJ ; Article Processing Charges ; Clarivate Analytics Master Journal List ; DOAJ Seal ; Essential Science Indicators ; Fees ; IF < 5 ; JCR ; SCOPUS ; Science Citation Index Expanded ; Web of Science Core Collection
Click to display QR Code for this record

The record appears in these collections:
Document types > Articles > Journal Article
Institute Collections > WIT DZNE > WIT DZNE-AG Roes
Documents in Process
Public records
In process

 Record created 2026-05-22, last modified 2026-05-22


Fulltext:
Download fulltext PDF Download fulltext PDF (PDFA)
Rate this document:

Rate this document:
1
2
3
 
(Not yet reviewed)