Students' Understanding and Beliefs About Pain Before and After a One-day Pain Science Education Conference: an Evaluation

Sponsor
Teesside University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05722587
Collaborator
(none)
160
2
3

Study Details

Study Description

Brief Summary

The beliefs held by students lead to behaviours in response to their pain which can be both helpful or a hindrance to how they manage their pain. The one-day education event aims to educate the cohort on the contemporary scientific understanding of persistent pain using a mixture of methods. It is hoped this event will result in an improvement in the alignment of beliefs and behaviours to contemporary understanding of persistent pain.

The principal aim is to evaluate the pre-post knowledge and beliefs about pain following a one-day pain education event in year 12 students, aged 16 or above.

Condition or Disease Intervention/Treatment Phase
  • Other: Pain science education
N/A

Detailed Description

The students will be asked to complete questionnaires three times relating to their understanding and beliefs relating and intended behaviour in the presence of pain. Once at the start of the conference and once at the end, then finally after 3 months. The questionnaire will gather demographic information (age, gender, ethnicity and any history of persistent pain). There will also be a series of multiple-choice questions relating to knowledge and beliefs about persistent pain. The three time points of questionnaire completion will see the students complete the same questionnaire except they will not have to repeat demographic questions. The questionnaire should take 5-10 minutes to complete each time. The questionnaires will be provided online and links will be provided to participants.

This is a non-randomised controlled trial and a second school selected as it is part of the same group of schools and equally matched according to the English Indices of Deprivation 2019. This school will complete the survey at the same time points.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
160 participants
Allocation:
Non-Randomized
Intervention Model:
Single Group Assignment
Intervention Model Description:
multi site, non-randomised controlled, mixed methods studymulti site, non-randomised controlled, mixed methods study
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
Students' Understanding and Beliefs About Pain Before and After a One-day Pain Science Education Conference: an Evaluation
Anticipated Study Start Date :
Mar 2, 2023
Anticipated Primary Completion Date :
Mar 2, 2023
Anticipated Study Completion Date :
Jun 2, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Pain education day

Pain education day, lecture and experiential

Other: Pain science education
High school students receiving a day of pain science education in multiple formats, lectures, experiential, completing a task which consolidates the information.
Other Names:
  • Pain neuroscience education
  • No Intervention: Control

    No intervention

    Outcome Measures

    Primary Outcome Measures

    1. Pain Beliefs Questionnaire (PBQ) [3 months]

      Helps to identify if participant beliefs are biomedical or biopsychosocial focussed, 12-item (Edwards et al, 1992, Walsh and Radcliffe, 2002). There are 2 scales within the PBQ: the organic beliefs scale has 8 items, with score ranges from 8-48, lower scores indicate less biomedical views and higher scores indicate more biomedical views. The psychological scale within the PBQ has 4 items with a score range of 4-24, a higher score indicates more biopsychosocial beliefs about pain and a lower score indicates less biopsychosocial beliefs.

    Secondary Outcome Measures

    1. Concept of Pain Inventory-Adult (COPI-Adult) [3 months]

      The Concept of Pain Inventory-Adult was designed for assessing knowledge and beliefs about pain science (Pate et al, 2022). It is a 13-item questionnaire. Higher COPI-Adult scores reflect greater alignment with contemporary pain science (Total scores can range from 0-52).

    Other Outcome Measures

    1. Vignette [3 months]

      Participants will be asked what actions they would take if they had pain with regards to medication, scans, daily activity, exercise and work either based on yes/no answers or four to five multiple choice answers. The percentage of recommendations in keeping with guidelines were measured from 0-100% with lower scores indicating intended behaviours that were not in keeping with guidelines.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    16 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes

    Inclusion Criteria: students at two specified schools in North Yorkshire who had been offered the pain study day or are in the control school in year 12

    Aged above 16. Providing consent to participate.

    -

    Exclusion Criteria:

    Students not providing consent.

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Teesside University

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Mrs Jagjit Mankelow, Lecturer in Rehabilitation Science, Teesside University
    ClinicalTrials.gov Identifier:
    NCT05722587
    Other Study ID Numbers:
    • 2022 Oct 11360 Mankelow
    First Posted:
    Feb 10, 2023
    Last Update Posted:
    Feb 10, 2023
    Last Verified:
    Feb 1, 2023
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Mrs Jagjit Mankelow, Lecturer in Rehabilitation Science, Teesside University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 10, 2023