- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03522857
Healthcare Professional Students' Knowledge and Attitudes Towards Chronic Pain Management.
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
Status
Detailed Description
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Middlesbrough, United Kingdom, TS1 3BX
- Teesside University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- pre-registration healthcare student, BSc or MSc.
Exclusion Criteria:
- post-registration students
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Teesside University
nursing, midwifery, physiotherapy, occupational therapy, diagnostic radiography, paramedics
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Glasgow Caledonian University
nursing, midwifery, physiotherapy, occupational therapy, diagnostic radiography, paramedics
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Northumbria University
nursing, midwifery, physiotherapy, occupational therapy
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University of Nottingham
Physiotherapy, nursing and midwifery
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Curtin University
Physiotherapy
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Notre Dame University
Physiotherapy
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University College Dublin
Physiotherapists
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Leeds Beckett University
Physiotherapists
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University College Cork
Physiotherapists
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Robert Gordon University
OT, Physio, Midwifery, Nursing, Diagnostic radiography
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University of Ulster
Physiotherapy
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University of Limerick
OT, Physio, Midwifery, Nursing, Diagnostic radiography, paramedic
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Revised Neurophysiology Quiz
Time Frame: 1 day
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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.
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1 day
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Health care providers Pain and Impairment Relationship Scale
Time Frame: 1 day
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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.
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1 day
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Biographic data
Time Frame: 1 day
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age in years
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1 day
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Biographic data (gender)
Time Frame: 1 day
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gender (male/female)
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1 day
|
Biographic data (discipline)
Time Frame: 1 day
|
discipline (nursing, midwifery, physiotherapy, occupational therapy, paramedics, diagnostic radiotherapy)
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1 day
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Biographic data (Degree qualification)
Time Frame: 1 day
|
level of study (BSc/MSc)
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1 day
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Biographic data (stage of study)
Time Frame: 1 day
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Year of study (first or final year)
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1 day
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Biographic data (Institute)
Time Frame: 1 day
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University of study
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1 day
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Jagjit Mankelow, MSc, Teesside University
Publications and helpful links
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
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
Studies a U.S. FDA-regulated device product
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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