The patient/caregiver partner surveys are designed to understand the actual experience of researchers when they partner with patients and caregivers on a project where the patients and/or caregivers are members of the research team. The questions are practical and look to identify behaviours that support productive partnerships. The researcher surveys are designed to understand the actual experience of researchers when they partner with patients and caregivers on a project where the patients and/or caregivers are members of the research team.
To assess current strategies, attitudes, facilitators, and barriers toward engaging patients in practice improvement efforts.
Multiple instruments meant at planning evaluation projects and to track progress; develop interviews, focus groups, questionnaires, surveys etc.; promote good practice and assure staff-led Patient Focus and Public Involvement work; ensure that learning points and actions are identified and implemented or take forward appropriately; plan, check and/or audit actions for evaluation findings; and improve practices of involvement.
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 assess the organizational Impact of patient involvement.
Following five factors influencing community participation (needs assessment, leadership, organisation, resource mobilisation and management), to assess participation in health care programmes. The tools can be used to compare the same programme at a different point in time, to compare observations by different evaluators, and/or to compare perceptions of different participants in the same programmes.