- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04587596
An Exploration of the Impact of Pain Education on GP Practice Staff
An Exploration of the Impact of Pain Education on GP Practice Staff: a Mixed Methods Study
The aim of the research project is to quantify GP practice staffs' knowledge of chronic pain, their attitudes towards people with chronic pain and their management of a hypothetical patient with chronic pain, following a pain education session.
The study also seeks to explore GP practice staffs' experience of receiving the pain education, their understanding of pain following the education and if they perceive the education session has impacted upon their daily practice.
Study Overview
Detailed Description
Inappropriate, biomedical based views of chronic pain are commonly held by health care professionals (HCPs) and these in turn can result in patients receiving sub-optimal care out of step with current guidelines. It has been found that healthcare professionals management techniques did not reflect recognised treatment guidelines and this was associated with their biomedical view of chronic pain.
Pain education/training sessions for health care staff may be an important step towards improving patient care for chronic pain. It has been found that there was improvement in nurses' knowledge after 2 different pain education sessions delivered to nurses however there was no long term follow up. Furthermore, no studies have targeted all members of staff at a GP surgery who will interact with the patient, and thus impact upon the care they receive.
Pain Neuroscience education (PNE) is an approach to pain education which uses pain science information to shift the belief system of the receiver away from a biomedical understanding of pain to a more biopsychosocial understanding of pain.
A number of studies have shown that this education can decrease biomedical attitudes in health care students. Thus, it may be that this education could produce similar positive effects in GP practice staff that could have positive implications for the care of patients with chronic pain.
Thus this study aims to assess the impact on attitudes and beliefs of pain education upon staff at a GP surgery in Middlesbrough. Attitudes and beliefs will be assessed before and after the delivery of education. In addition participants will be invited to attend one of two focus groups to further discuss their findings or thoughts about the lecture.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Middlesbrough, United Kingdom, TS5 6HA
- Linthorpe Surgery
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria
- Clinical non-NHS staff at a Middlesbrough GP Surgery.
Exclusion Criteria
- Non-clinical staff at a Middlesbrough GP surgery and staff who are not directly employed by the Surgery.
Study Plan
How is the study designed?
Design Details
- Observational Models: Case-Only
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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Clinical staff
All clinical staff employed at one surgery in Middlesbrough, UK who wish to participate
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70 minute lecture about chronic pain and one focus group afterwards
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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HC-PAIRS
Time Frame: 70 minutes
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Health Care Providers Pain and Impairment Relationship Scale - assessing attitudes and beliefs towards pain using a 13 item validated questionnaire.
High score is a worse outcome.
Scores range from 13-91.
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70 minutes
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Revised pain neurophysiology quiz
Time Frame: 70 minutes
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Measures knowledge of pain physiology using a 12 point validated questionnaire.
Low score is poor sign.
Scores range from 0-12.
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70 minutes
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case vignette
Time Frame: 70 minutes
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Measures clinical practise behaviours in pain management.
A validated proxy measure of clinical behaviour, MCQ weighted as appropriate or inappropriate according to current national clinical guidelines.
A low score is good, and scores range from 4 to 20.
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70 minutes
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Interviews - qualitative assessment
Time Frame: 1 hour
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Interviews to assess perception and intended application of lecture material
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1 hour
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: J Mankelow, MSc, Teesside University
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 205/18
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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