- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06151678
An Evaluation of a Public Health Campaign Related to Persistent Pain in the United Kingdom
The goals of this study are
- To define what the public perceptions of persistent pain using a national survey
- Explore relationships between the reported pubic beliefs and demographic factors collected.
- To evaluate the impact of a public health campaign to increase awareness of persistent pain and develop understanding of pain that aligns with contemporary science.
Study Overview
Status
Intervention / Treatment
Detailed Description
This study included a cross sectional survey of the UK population to understand what the beliefs are regarding persistent pain. This survey will be distributed electronically using social media and to a Scottish council. Differences in beliefs will be explored using the demographic data collected.
The second aspect of the study is the evaluation of a public health campaign called 'Flippin Pain'. This study component included the evaluation of online webinars with pre, post, 3 month, 6 month and 12 month longitudinal data collection. One of the online seminars also included the qualitative evaluation using semi structured interviews.
The third part of the study was the evaluation of a community outreach tour in the county of Lincolnshire, United Kingdom. This included the collection of pain belief data before an in person seminar, immediately afterwards, then at 3 months. Semi structured interviews were also conducted with participants who attended the webinars. As part of the outreach tour an interactive pop up tent gave members of the public an understanding of pain using practical demonstrations. The was evaluated using short semi structured interviews along with written summaries offered by the participants before and immediately after experiencing the practical demonstrations.
After the community outreach tour, two focus groups were conducted with the campaign volunteers with an aim to understand the experience of those involved. The focus groups asked the participants to reflect on the successes and challenges of delivering a community based public health outreach tour.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Middlesbrough, United Kingdom, TS1 3BX
- Teesside University
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Cross sectional survey - Adults over the age of 18 that respond to an electronic survey link posted on FaceBook groups and employees of a Scottish council.
Webinars and Seminars - Individuals who attended an education webinar or seminar related to persistent pain.
Brain Bus - Individuals who engaged in the interactive experience to learn about persistent pain.
Focus Groups - A total of 20 volunteers who supported the community outreach tour in the English county of Lincolnshire.
Description
Inclusion Criteria:
- UK cross sectional survey - All adults over the age of 18 who are the capable of offering informed consent)
- Online webinar study - Adults over the age of 18 who attend an online webinar related to persistent pain
- Community outreach tour seminar - Adults over the age of 18 who attend an in person seminar
- Brain Bus - Adults over the age of 18 who experience the interactive demonstrations relating to persistent pain
- Focus Groups - Volunteers who participated in the Flippin Pain community outreach tour within the county of Lincolnshire
Exclusion Criteria:
- Individuals younger than 18 years of age.
- For the cross sectional UK survey, adults who lived outside of the UK were excluded.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
UK population survey
The UK population who accessed the electronic survey link disseminated via social media and via a gatekeeper at a Scottish council
|
|
Participants attending online webinars
Individuals who signed up for an online webinar related to persistent pain.
This group offered quantitative feedback via online surveys and qualitative data via interview.
|
Pain education was offered to health professionals and the general public using with a focus on pain neuroscience.
This was offered with a lecture from pain scientists, personal reflections from individuals with lived experience and health care professionals.
|
Participants who attended in person seminars during a community outreach tour
Individuals who attended six different venues across the English county of Lincolnshire.
This group offered quantitative feedback via paper and online surveys and qualitative data via interview.
|
Pain education was offered to health professionals and the general public using with a focus on pain neuroscience.
This was offered with a lecture from pain scientists, personal reflections from individuals with lived experience and health care professionals.
|
Brain bus cohort
Participants who attended a pop up interactive tent with practical demonstrations to improve pain related knowledge.
This group offered quantitative feedback via paper postcards and qualitative data via interview.
|
Pain education was offered to health professionals and the general public using with a focus on pain neuroscience.
This was offered with a lecture from pain scientists, personal reflections from individuals with lived experience and health care professionals.
|
Community outreach tour volunteers
Focus groups were arranged for those who volunteered to lead and deliver the community outreach tour
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Pain Beliefs Questionnaire
Time Frame: Used within the cross sectional survey and pre and post webinars and seminars. This has been administered immediately before the webinar or seminar, immediately after the webinar or seminar, then at 3 month, 6 month and 1 year.
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A validated survey to ascertain pain beliefs from the general population
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Used within the cross sectional survey and pre and post webinars and seminars. This has been administered immediately before the webinar or seminar, immediately after the webinar or seminar, then at 3 month, 6 month and 1 year.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
HC-PAIRS
Time Frame: This is administered online immediately prior to adttendance of an online webinar. Immediately after the webinar. Then further administration at 3 month, 6 month and 1 year.
|
A validated survey to ascertain the pain beliefs of healthcare professionals.
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This is administered online immediately prior to adttendance of an online webinar. Immediately after the webinar. Then further administration at 3 month, 6 month and 1 year.
|
Osteoarthritis Conceptual Scale
Time Frame: This is administered online immediately prior to attendance of an online webinar. Immediately after the webinar. Then further administration at 3 month, 6 month and 1 year.
|
A 33 item survey to ascertain beliefs regarding knee osteoarthritis
|
This is administered online immediately prior to attendance of an online webinar. Immediately after the webinar. Then further administration at 3 month, 6 month and 1 year.
|
Collaborators and Investigators
Sponsor
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- TeessideUniversitySOHLS
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
- CSR
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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