- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04903379
Flippin Pain: A Public Health Campaign Evaluation
May 23, 2021 updated by: Nick Livadas, Teesside University
An Evaluation of an Online Webinar Aimed at Shifting the Beliefs of the UK Population Regarding Persistent Pain
An online webinar aiming to improve the public beliefs related to persistent pain will be offered to members of the public in the UK via social media and targeted via written invitation to individuals on a waiting list for pain and musculoskeletal services in Ayrshire and Arran, Scotland.
Study Overview
Detailed Description
Flippin Pain is a UK based public health campaign which aims to shift the populations perception related to persistent pain to one that is aligned with contemporary pain science understanding.
The webinar will be presented by a panel consisting of people with a history of persistent pain and healthcare professionals with experience of treating persistent pain.
The webinar will be advertised on social media.
When registrants receive their confirmation email confirming their place they will be notified of of the invitation to participate.
This link within the email will take them to an online participant information sheet.
Once this is read they may decide to proceed with an online survey which would take 10 minutes to complete.
This survey will include some non identifiable demographic data and the Pain Beliefs Questionnaire (PBQ).
The PBQ is a validated tool that does not require a license to use.
The survey will be administered immediately after the webinar, at 3, 6 and 12 months to assess for longitudinal changes in pain beliefs.
Another recruitment strategy will be the posted invitation to individuals on a National health Service waiting list.
Both groups will complete the same survey questions.
The last question of the survey will request the participants email so that future surveys can be sent and the follow ups linked by participant.
Individuals will also be asked within the survey if they consent to further contact about the opportunity to answer questions vie a telephone/online interview related to their experience of the webinar.
Purposive sampling will be used to recruit 15-20 individuals for a semi structured interview.
Study Type
Interventional
Enrollment (Anticipated)
1000
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Ayrshire And Arran
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Kilmarnock, Ayrshire And Arran, United Kingdom, KA2 0BE
- Ayrshire and Arran NHS Scotland
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Contact:
- Emma Mair, BSc
- Email: emma.mair@nhs.net
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Resident within the United Kingdom
- Over the age of 18 years
Exclusion Criteria:
- Unable to read the English version of the surveys
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Other: Pain science education and self management strategies
The intervention will be educational in the form of the provision of contemporary pain science education and supportive advice from people with a history of persistent pain.
The duration of the webinar will be 90 minutes.
|
An explanation of contemporary pain science and a description of effective treatment strategies used by people with a history of persistent pain.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Pain Beliefs Questionnaire
Time Frame: 10 minutes to complete
|
A validated self reported questionnaire
|
10 minutes to complete
|
Pain self efficacy questionnaire
Time Frame: 10 minutes to complete
|
A validated self reported questionnaire
|
10 minutes to complete
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Anticipated)
August 1, 2021
Primary Completion (Anticipated)
August 1, 2022
Study Completion (Anticipated)
December 1, 2022
Study Registration Dates
First Submitted
May 23, 2021
First Submitted That Met QC Criteria
May 23, 2021
First Posted (Actual)
May 26, 2021
Study Record Updates
Last Update Posted (Actual)
May 26, 2021
Last Update Submitted That Met QC Criteria
May 23, 2021
Last Verified
May 1, 2021
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 6167
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
IPD Plan Description
Non identifiable data may be shared.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
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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