An Evaluation of a Public Health Campaign Related to Persistent Pain in the United Kingdom

November 27, 2023 updated by: Nick Livadas, Teesside University

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

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

Observational

Enrollment (Actual)

800

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

      • Middlesbrough, United Kingdom, TS1 3BX
        • Teesside University

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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

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

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

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.
A validated survey to ascertain pain beliefs from the general population
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.
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

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 (Actual)

August 1, 2020

Primary Completion (Actual)

June 1, 2022

Study Completion (Actual)

June 1, 2022

Study Registration Dates

First Submitted

December 18, 2022

First Submitted That Met QC Criteria

November 27, 2023

First Posted (Actual)

November 30, 2023

Study Record Updates

Last Update Posted (Actual)

November 30, 2023

Last Update Submitted That Met QC Criteria

November 27, 2023

Last Verified

November 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • TeessideUniversitySOHLS

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

Anonymised data may be shared from the survey responses.

IPD Sharing Time Frame

When the evaluation is completed and submitted to a peer review journal. Estimated 2024.

IPD Sharing Access Criteria

Additional data beyond what is included in the results section of the manuscript can be made available within the supplementary files.

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • ICF
  • CSR

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

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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