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Application information packPatient and Public Voice (PPV) Partner level 4 roles within the Clinical Policy Units Cardiac ProgrammeIntroduction Thank you for your interest in becoming a Patient and
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How to fill out patient and public involvement

01
Identify the purpose and goals of the patient and public involvement.
02
Recruit a diverse group of patients and members of the public to participate.
03
Provide training and support for participants to ensure they can contribute effectively.
04
Clearly communicate the expectations and roles of participants.
05
Create opportunities for input and feedback throughout the process.
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Acknowledge and incorporate the input and feedback received from patients and the public.
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Evaluate the impact of the patient and public involvement on the project or decision.

Who needs patient and public involvement?

01
Researchers conducting clinical trials or studies that involve human participants
02
Healthcare providers looking to improve patient care and services
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Policy makers developing health strategies and programs
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Health organizations seeking to better understand and meet the needs of their communities

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Patient and public involvement (PPI) refers to the active collaboration of patients and the public in the design, implementation, and evaluation of health and social care services. It aims to ensure that the perspectives and needs of patients are taken into account in decision-making processes.
Organizations or individuals conducting research or projects that involve patient and public participation are typically required to file patient and public involvement reports. This includes academic institutions, healthcare providers, and research teams.
To fill out a patient and public involvement report, researchers should outline the strategies used to engage patients and the public, detail their contributions, provide feedback received, and describe how this engagement shaped the research process.
The purpose of patient and public involvement is to enhance research quality, ensure that research addresses the needs of the community, improve the relevance of findings, and foster trust between researchers and the public.
Reports on patient and public involvement should include information about the nature and level of involvement, how participants were recruited, the methods used to gather their input, and the outcomes of their engagement.
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