Sammenlign metoder

	Social Role Participation Questionnaire	Indvirkning på Deltagelse og Autonomi
Fagområde	Rehabiliteringsvidenskab	Rehabiliteringsvidenskab
Familie	Process / pipeline	Process / pipeline
Oprindelsesår	2004	2001
Ophavsperson	Lyons, Sayer, et al.	Cardol, de Haan, de Groot, de Jong
Type	Self-report or Interview	Self-report or Proxy
Oprindelig kilde	Lyons, K. S., & Sayer, A. G. (2005). How does loss matter? The experience of spouse loss among family caregivers of persons with Alzheimer's disease. American Journal of Alzheimer's Disease and Other Dementias, 20(5), 273–290.	Cardol, M., de Haan, R. J., de Jong, B. A., van den Bos, G. A., & de Groot, I. J. (2001). Psychometric properties of the Impact on Participation and Autonomy questionnaire. Archives of Physical Medicine and Rehabilitation, 82(2), 210–216.
Aliasser	SRPQ, Social Role Questionnaire	IPA, IPA-Scale
Relaterede	5	5
Resumé	The Social Role Participation Questionnaire (SRPQ) is a brief, self-report instrument designed to measure the extent to which individuals participate in and derive meaning from key social roles (family member, friend, worker, volunteer, community member, leisure participant). Developed by Lyons, Sayer, and colleagues, SRPQ is used in traumatic brain injury, stroke, and other disability research to assess how completely a person has resumed their valued life roles post-injury or illness.	The Impact on Participation and Autonomy (IPA) scale is a validated, patient-centered measure designed to quantify how chronic conditions or disabilities affect an individual's autonomy and participation in five key life domains: autonomy, mobility, occupation, social relations, and recreation. Developed in the Netherlands by Cardol and colleagues, it operationalizes the WHO handicap concept (now called 'participation restriction') and is widely used in rehabilitation, chronic disease management, and policy evaluation across Europe.