Healthcare Professional Students' Knowledge and Attitudes Towards Chronic Pain Management.

October 11, 2019 updated by: Mrs Jagjit Mankelow, Teesside University

Measuring Healthcare Professional Students Knowledge and Attitudes Towards Chronic Pain Management.

Chronic pain affects from one third to one half of the population in the UK (Fayaz et al, 2016). The cost and burden of chronic pain is significant to health services worldwide. The affects of chronic pain are widespread upon the lives of those affected. Health professionals need to be better equipped than at present to manage pain and current chronic pain management knowledge in healthcare is poor. Briggs et al 2011 described the hours of pain education delivered at undergraduate level as 'woefully inadequate'. The International Association for Study of Pain (IASP) defined curricula for pain education at undergraduate level 6 years ago but current levels of knowledge at undergraduate health professional level are not widely known. This study aims to establish this at the outset of a pre-registration health professional courses and at the end of these courses.

This study aims to identify the baseline knowledge and attitudes of pre-registration healthcare students in Universities throughout UK and Ireland toward chronic pain management. The disciplines targeted are nursing, midwifery, physiotherapy, occupational therapy, diagnostic radiography and paramedics.

It is a cross sectional study that compares attitudes and knowledge of first year and final year pre-registration healthcare students in the UK and Ireland. These parameters are measured using the HC-PAIRS measure and Revised Neurophysiology Questionnaire respectively. In addition anonymous data is collected pertaining to participant characteristics which are institute of study, age, gender, level and discipline of study to enable a comparison between these parameters.

Study Overview

Detailed Description

Chronic pain is characterised by a protective mechanism of the neuro-immune-endocrine systems potentially exacerbated by loading exposures, conditioning, psychological, socio-economic, lifestyle, comorbid mental health and non-modifiables such as genetics, (O'Sullivan et al 2016). Pain education can be a useful basis for helping patients to manage their symptoms and return to good daily function. However a biomedical approach to chronic pain persists in medical communities, whilst persistent pain populations increase and incidences of opioid addiction are growing secondary to poor pain management. Biomedical models of pain are likely to induce fear avoidant behaviour and exacerbate chronicity (Wertli et al 2014). In order to change the prevailing biomedical approach to chronic pain the International Association for the Study of Pain (IASP) have provided detailed pain curricula content for different medical and allied health professional courses. Briggs et al (2015) found that out of 15 'representative European countries' less than a handful of universities from 3 countries had implemented distinctly identifiable pain education teaching. However they may be other forms of pain education that are taking place in pre-registration healthcare professional education. This study aims to establish the levels of chronic pain management knowledge and attitudes prevail in the UK and Ireland amongst pre-registration healthcare professionals.

Study Type

Observational

Enrollment (Actual)

1150

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

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

N/A

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

University students in UK and Ireland.

Description

Inclusion Criteria:

- pre-registration healthcare student, BSc or MSc.

Exclusion Criteria:

- post-registration students

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
Teesside University
nursing, midwifery, physiotherapy, occupational therapy, diagnostic radiography, paramedics
Glasgow Caledonian University
nursing, midwifery, physiotherapy, occupational therapy, diagnostic radiography, paramedics
Northumbria University
nursing, midwifery, physiotherapy, occupational therapy
University of Nottingham
Physiotherapy, nursing and midwifery
Curtin University
Physiotherapy
Notre Dame University
Physiotherapy
University College Dublin
Physiotherapists
Leeds Beckett University
Physiotherapists
University College Cork
Physiotherapists
Robert Gordon University
OT, Physio, Midwifery, Nursing, Diagnostic radiography
University of Ulster
Physiotherapy
University of Limerick
OT, Physio, Midwifery, Nursing, Diagnostic radiography, paramedic

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Revised Neurophysiology Quiz
Time Frame: 1 day
12 point pain knowledge quiz devised originally by Moseley 2003 to assess knowledge of biological mechanisms of pain. Revised and reduced in 2013 by Catley et al. The lowest score is 0 and the highest would be 12 on a scale of 0-12. There are no subscales.
1 day
Health care providers Pain and Impairment Relationship Scale
Time Frame: 1 day
A 13 question, 7 point Likert scale and a validated questionnaire to assess health care providers' attitudes and beliefs about the relationship between pain and impairment. The scale ranges in outcome from 0-90, higher scores representing a stronger belief in the relationship between chronic pain and disability (a 'worse outcome') and lower scores representing a reduced belief on this relationship thus a 'better outcome'. There are no subscales.
1 day

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Biographic data
Time Frame: 1 day
age in years
1 day
Biographic data (gender)
Time Frame: 1 day
gender (male/female)
1 day
Biographic data (discipline)
Time Frame: 1 day
discipline (nursing, midwifery, physiotherapy, occupational therapy, paramedics, diagnostic radiotherapy)
1 day
Biographic data (Degree qualification)
Time Frame: 1 day
level of study (BSc/MSc)
1 day
Biographic data (stage of study)
Time Frame: 1 day
Year of study (first or final year)
1 day
Biographic data (Institute)
Time Frame: 1 day
University of study
1 day

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Jagjit Mankelow, MSc, Teesside University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the 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)

November 15, 2017

Primary Completion (ACTUAL)

September 30, 2019

Study Completion (ACTUAL)

September 30, 2019

Study Registration Dates

First Submitted

April 18, 2018

First Submitted That Met QC Criteria

April 30, 2018

First Posted (ACTUAL)

May 11, 2018

Study Record Updates

Last Update Posted (ACTUAL)

October 15, 2019

Last Update Submitted That Met QC Criteria

October 11, 2019

Last Verified

October 1, 2019

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • SA 144/17

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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