পদ্ধতির তুলনা করুন

	অংশগ্রহণ ও স্বায়ত্তশাসনের উপর প্রভাব	Participation Scale
ক্ষেত্র	পুনর্বাসন বিজ্ঞান	পুনর্বাসন বিজ্ঞান
পরিবার	Process / pipeline	Process / pipeline
উদ্ভবের বছর	2001	2006
প্রবর্তক	Cardol, de Haan, de Groot, de Jong	van Brakel, Officer, Nicol
ধরন	Self-report or Proxy	Self-report or Interview
মৌলিক উৎস	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.	van Brakel, W. H., Officer, A., & Nicol, M. (2020). Handbook of Disability and Health Equity: Toward Achieving the Sustainable Development Goals. Frontiers Media. Chapter: Participation.
অপর নাম	IPA, IPA-Scale	P-Scale, Participation Scale (van Brakel)
সম্পর্কিত	5	5
সারসংক্ষেপ	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.	The Participation Scale (P-Scale) is a brief, 8-item measure designed to assess restrictions in participation across social and occupational roles in people with chronic conditions or disabilities. Developed by van Brakel and colleagues, the P-Scale is widely used in low- and middle-income country (LMIC) settings and in global health research where conciseness and cross-cultural applicability are essential. It offers a quick, validated snapshot of how much a condition limits a person's engagement in work, self-care, communication, and social participation.