We are always keen to involve people in our research at OH CRF.
You can find out more about how to take part in research, get involved with our engagement activities or hear what we have done in response to your feedback below.
Please click on the headings below to find out more.
Taking part in research
We run several types of studies in mental and cognitive health.
Some studies involve people with a specific diagnosis and others are open to people without a diagnosis.
There are many ways you can get involved in research at OH CRF.
If you are interested in taking part in research, please email us: [email protected]
When your participation in research ends, we offer an Information Leaflet (pdf download), co-produced with the ENGAGE PPI group, for further links and advice.
Patient and Public Involvement (PPI)
What is PPI?
We believe your voice matters. We are fully committed to working with patient and public contributors. Contributors include patients, potential patients, carers, research participants and advocacy groups.
PPI aims to ensure that research is carried out ‘with’ or ‘by’ members of the public rather than ‘to’, ‘about’ or ‘for’ them.
PPI improves the quality of our research by making sure that research is delivered and communicated in accessible, person-centred ways. This practice helps develop research that better serves the needs and interests of our community.
The Engage group
The Engage group aims to improve the experience of research participants, supporting our researchers to develop a friendly and comfortable environment. We usually meet every two months. Our meetings are hybrid, with some people attending in person and others joining via Teams. We are always keen to hear from people who are interested in joining our group.
Below, members of the Engage group share their experiences of their involement.
Amy Wizard Ponter

Research is a powerful thing. It is about progress. It is about discovery. It is about improvements. It is about working together across spaces, people and platforms.
Oxford Health Clinical Research Facility (OH CRF) is a dedicated centre for improving mental and cognitive health treatments through clinical research and is the only National Institute for Health and Care Research (NIHR) supported CRF dedicated to mental health.
At the core of OH CRF’s research is patient and public involvement. Without people, mental health research cannot take place, whether they are participants in a study/trial or whether they are helping to shape research itself.
Patient involvement is about clinicians, researchers, patients and the public working together with respect and equity at heart.
I am fortunate that I am a part of this work. I help to advise and guide various aspects of the research process, bringing lived experience and insight. Whether through the Engage group or with researchers directly, research can be both improved and enhanced by patient involvement.
It’s not just about being asked for comment after something has already happened. It is about discussions, staff bringing ideas and questions to the group and asking for real thoughts, real experiences. Suggestions are invited, but more than that, researchers are eager for them. They want their work to be shaped in tangible and beneficial ways through consultation.
Engage group meetings have busy agendas with many topics to discuss. Researchers want to present their proposals or provide updates on where they have progressed. OH CRF staff often ask for opinions about the facilities and how they can be enhanced to improve participant experience.
We are regularly invited to review information or documentation, and our advice is considered.
I’ve been lucky to have been part of a study walk through, providing input on a study concept. I had also created a video to be used at a conference to share information on the work of the group, which was a chance to showcase how OH CRF actively apply public engagement in their work. A recent focus group centred on the disproportionate impact of certain mental health diagnoses on an increased likelihood of developing diabetes.
Helping with research is valuable. I’d advocate for anyone to explore opportunities to get involved. If you wish to make a difference and impact research and its outcomes in positive and grounded ways, then consider becoming part of Engage.
Kate Brunwin

I first heard about the Engage group through a forum I attend called ‘Our Voice’. The forum is for Experts by Experience with Oxford Health. I thought it sounded interesting and a new way to use my experience to inform research. So, I came to a meeting and enjoyed it so much I stayed for almost 2 years now! I support by lending my voice to different projects and to supporting the CRF in their work. I give ideas to various projects based on my experiences and bring a live experience viewpoint to the meetings.
I am always keen to use my lived experience to further services and research. I love to use what could often be negative experiences for something positive and good. I particularly like to support research further so that we can all find better ways of helping people with their mental health. I enjoy hearing the different work of the CRF as it is very engaging and interesting.
I would encourage anyone wanting to join the Engage group to go for it! It is very interesting, your voice is needed and important, there is always something new to learn. It has been a great experience, and I would highly recommend it.
I recently supported a research project at the CRF. They wanted some help with a study they are doing, looking at using different anti-psychotic medications. They specifically wanted someone to help to check it would run well and made sense for the participants and was tailored to their needs. I met with the researchers, and we went through all the research questionnaires together and how the research will work for participants. I was able to give some advice about the running of the project for those taking part and to draw on my own experiences of mental health to ensure the project worked well.
There are also ad-hoc PPI opportunities, for example reviewing information sheets, supporting on staff interview panels, and attending mock research visits to share your perspective before research participants attend these visits.
Patient and Public Involvement, Engagement and Participation strategy
You can download our Patient and Public Involvement, Engagement and Participation strategy here.
What people say about us
111 participants completed our Q1 2025 participant feedback survey
| This is what they said | % of respondents choosing agree/strongly agree |
|---|---|
| The CRF was easy to find | 97% |
| The CRF was comfortable | 100% |
| The CRF was accessible | 88% |
| The CRF was welcoming | 97% |
| I understood the aims of the visit today | 100% |
| Information was communicated effectively before my visit | 97% |
| Information was communicated effectively during my visit | 97% |
| My participation was worthwhile | 91% |
| I would recommend participating in research at the CRF to family and friends | 97% |
Quotes from participants and contributors
What have we done as a result of your feedback?
















