ClinicalTrials.gg
CompletedNCT05722587Updated Jul 20, 2023

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

An interventional study of Pain science education in Pain, Chronic, sponsored by Teesside University. Completed at 1 site in United Kingdom. Open to participants aged 16 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-07-20.

Sponsored by Teesside University · Not applicable, Interventional, and Basic science

Phase
Not applicable
Study type
Interventional
Enrollment
167
Allocation
Non-randomized
Ages
16 Years and older
Sex
All
01

Study 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.

Read the 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.

02

Conditions studied

  • Pain, Chronic

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Keywords

  • pain knowledge
  • pain beliefs
  • pain behaviour
  • experience of intervention
03

In context

Chronic Pain

2,999 studies on the registry are indexed under Chronic Pain; 706 are open to participants now.

This study's enrollment of 167 is above the median of 60 across 2,209 interventional studies indexed under Chronic Pain.

Browse Chronic Pain studies →

Lead sponsor

Teesside University is the lead sponsor of 55 studies on the registry; 10 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
16 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Students at two specified schools in North Yorkshire who had been offered the pain study day in year 12 or are in the intervention or control school in year 12 or 13
  • Aged above 16.
  • Providing consent to participate.

Exclusion criteria

Exclusion Criteria:

  • Students not providing consent.
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
167 participants (actual)

Study arms

  • Experimental
    Pain education day

    Pain education day, lecture and experiential

    Other: Pain science education

  • No intervention
    Control

    No intervention

Interventions

  • OtherPain science education

    High school students receiving a day of pain science education in multiple formats, lectures, experiential, completing a task which consolidates the information.

    Also known as: Pain neuroscience education

06

What researchers measure

Primary outcomes

  1. Pain Beliefs Questionnaire (PBQ)

    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.

    Time frame: 3 months

Secondary outcomes

  1. Concept of Pain Inventory-Adult (COPI-Adult)

    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).

    Time frame: 3 months

Other outcomes

  1. Vignette

    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.

    Time frame: 3 months

07

Study locations

1 site
  • Teesside University
    Middlesbrough, TS1 3BX, United Kingdom
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Mar 2023 to primary completion in Mar 2023, 0 months.

Of 1,209 non-industry interventional studies with no phase under Chronic Pain, half reached primary completion within 21 months of starting (the median), counting those still running; a quarter within 9 and three quarters within 39. This study's 0 months is below that.

Counting every sponsor, half of 1,296 studies reached it within 21 months; a quarter within 9 and three quarters within 39.

How these figures are worked out, and which studies are left out of them.

Registered
Feb 1, 2023
First posted
Feb 10, 2023
StartActual
Mar 2, 2023
Primary completionActual
Mar 2, 2023
CompletionActual
Jun 2, 2023
Last update
Jul 20, 2023
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jul 20, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05722587
Lead sponsor
Teesside University
Responsible party
Mrs Jagjit Mankelow (Lecturer in Rehabilitation Science, Teesside University) — Principal investigator
First posted
Feb 10, 2023
Start date
Mar 2, 2023
Primary completion
Mar 2, 2023
Completion
Jun 2, 2023
Last update
Jul 20, 2023

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jul 2023. You cannot join it, but the record below documents what was studied.

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