Public Involvement in Privacy (PIP) panel – a year on – small challenges, big achievements and ongoing developments…
By Lorraine Wright, Lecturer in Psychology/PhD candidate/Research Assistant in Psychology, Edge Hill University It’s a year since we wrote a blog about the PIP panel. An integral part of the AP4L project, the PIP panel is based on a public involvement model adopted as routine practice within health and social care and associated research (UK Standards for Public Involvement, National Institute for Health and Care Research (NIHR), 2019). The PIP panel has been developed and adapted to meet the project's requirements while still keeping the public involvement model’s standards at the core of the panel. Comprised of members of the public who are ‘experts by experience, ’ the PIP panel has eight public partner members, two for each of the transitions involved in the study (serious illness, leaving the forces, relationship breakdown, and coming out as LGBT+). The group meets bi-monthly online for an hour. Over the last 22 months, the PIP panel has met 11 times, averaging seven