An observational study in Facial Pain, sponsored by Walton Centre NHS Foundation Trust. Completed at 1 site in United Kingdom. Per ClinicalTrials.gov, last updated 2026-09-24.
Sponsored by Walton Centre NHS Foundation Trust · Observational
A study consisting of up to 3 focus groups, consisting of 6-8 people to facilitate an open discussion regarding the experience of attending a specialist facial pain management programme, both in terms of attendance of the programme itself, as well as any impact on pain management in day to day life.
Chronic pain (CP) is a common condition causing significant distress and disability. Pain has been defined by the International Association for the Study of Pain (IASP), as 'an unpleasant sensory and emotional experience associated with actual or potential tissue damage, or described in terms of such damage. Pain remains essential for survival and facilitating medical diagnoses.
However, when acute pain outlasts the normal time of healing, it can become chronic. Chronic or persistent pain has been defined as 'continuous, long term pain of more than 12 weeks or after the time that healing would have been thought to have occurred in pain after trauma or surgery'. The definition of CP underlines the fact that emotional aspects are not additional to the experience of pain but are part of the sensation itself.
Psychological factors influence how people react to and report pain and result in coping strategies which may be helpful or destructive in maintaining function. The complex combination of emotions, thoughts and pain sensation manifests itself as pain behaviour. Pain, as a sensory experience, varies in its severity and life impact according to the individual's subjective meaning associated with a pain situation, his or her emotional responses, the attention given to the pain, and other personal appraisals. There is a strong evidence base for the effectiveness of pain management programmes (PMP's) underpinned by cognitive behavioural approaches in terms of improving patients well-being despite the presence of pain.
However, there is a relative lack of research specifically into cognitive behaviourally informed pain management treatment exclusively aimed at patients diagnosed with chronic facial pain. Some specialist PMP's focus exclusively on specific chronic pain diagnoses such as facial pain, whereas other PMP's offer treatment to patients with a broad range of chronic pain diagnoses. There is also little research into the relative advantages or disadvantages of these more specialist approaches. Systematic reviews have also suggested that further research is required to gain insight into the influence of specific components of PMP treatment on clinical outcomes.
Through gaining insight into service users experience of attending a specialist facial PMP, we hope to build on research in this area. This insight may have implications both for questions regarding the utility of more specialist PMP's and specific aspects of facial PMP's that patients find beneficial. In turn this may help guide our own service provision in future.
182 studies on the registry are indexed under Facial Pain; 61 are open to participants now.
This study's enrollment of 11 is below the median of 101 across 42 observational studies indexed under Facial Pain.
Browse Facial Pain studies →Walton Centre NHS Foundation Trust is the lead sponsor of 17 studies on the registry; 2 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Service users who have attended a specialist facial pain management programme.
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Patient perceptions of the effectiveness of pain management programmes and associated sessions (Physiotherapy, occupational therapy, psychology)
Audio recorded focus group sessions transcribed and broken down into qualitative research data. Themes from this data will then be identified. Questions asked in these focus group sessions include; * What aspects of the pain management group were most helpful? * What were the least helpful? * How did you find the structure of the pain management group? * What were your experiences of the physiotherapy / occupational therapy / psychology sessions? * What would you change about the programme to improve it further?
Time frame: From date of completion of facial pain management programme at WCFT to attendance at focus group. This time frame can be 1-10 years based on active participant.
Ran from Jul 2017 to primary completion in Aug 2018, 13 months.
How these figures are worked out, and which studies are left out of them.
This study is completed, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.
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Walton Centre NHS Foundation Trust