The patient/caregiver and researcher 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. Surveys of researchers have the same goal: to understand their experience when associating with patients/caregivers.
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 taken forward appropriately; plan, check and/or audit actions for evaluation findings; and improve practices of involvement.
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 explore attitudes about patient and family involvement as advisors and/or members of improvement and redesign teams.
To assess performance and compliance. The scorecard is divided into five consecutive goals necessary to realize a culture of engagement: (1) value public input, (2) clarity of purpose, (3) well-defined roles, (4) accountability and (5) responsiveness and good communication.
Two instruments meant to (1) routinely evaluate team collaboration skills and assess your growth, and (2) assess how your team is doing at encouraging participation and collaboration at your meetings.
