To assist your organisation to improve consumer and community participation policies and practice; to identify a broad range of opportunities for participation; to assess and develop your organisation’s commitment and capacity to involve and support consumers and communities in a range of planning, implementation, and evaluation activities.
To track the impact of public involvement in research in this sample from project inception through to completion where possible and, at a minimum, for complete stages of the research process (design, recruitment, data collection, analysis, dissemination). Identify the desired outputs and outcomes of public involvement in research in the sample from multiple stakeholder perspectives (e.g. members of the public, researchers, research managers).
To assess the organizational impact of patient involvement.
To assess the organizational impact of patient involvement.
To help research teams to evaluate dimensions of quality service user involvement in the contexts they are working within.
Following five factors influencing community participation (needs assessment, leadership, organisation, resource mobilisation and management), to assess participation in health care programs. The tools can be used to compare the same program at different points in time, to compare observations by different evaluators, and/or to compare perceptions of different participants in the same programs.
Consists of (1) an Organization questionnaire to assess the organization’s capacity for, and culture of public and patient engagement; (2) a Participant questionnaire to obtain participants’ assessments of key features of the engagement activity that they have participated in, and (3) a Project questionnaire to assess the planning, execution and impact of the engagement activity after it has been completed.
To help researchers assess the impacts of involving members of the public in health and social care research.
