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

Status

Not yet recruiting

Conditions

Intervention / Treatment

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
      • Kilmarnock, Ayrshire And Arran, United Kingdom, KA2 0BE

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.

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.

Clinical Trials on Pain, Chronic

Clinical Trials on Education

3
Subscribe