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CompletedNCT06821022Updated May 15, 2026

The Impact of Pain Neuroscience Education on Physical Therapy Students' Knowledge, Attitudes, Beliefs, and Behaviors Towards Pain: A Randomized Controlled Trial

An interventional study of Pain Neuroscience Education and Red Flags Education in Healthy Subjects, sponsored by The Hashemite University. Completed at 1 site in Jordan. Per ClinicalTrials.gov, last updated 2026-05-15.

Sponsored by The Hashemite University · Not applicable, Interventional, and Health services research

From the registry’s dates

  • Registered 11 months after the study started (first participant enrolled Feb 2024, registered Feb 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
120
Allocation
Randomized
Sex
All
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Study summary

This study investigates the effect of pain neuroscience education (PNE) on pain knowledge, attitudes, beliefs and behaviors among undergraduate physiotherapy students in Jordan

Read the detailed description

Physiotherapy students at the Hashemite University will be randomly assigned into either pain neuroscience education or control lectures groups. Both groups will receive a 70-min didactic group-lecture. The control group will receive education about red-flags which are special screening questions for serious pathology. The red-flags education will discuss tissue pathology and triage for back pain classification. Neurophysiology and the biopsychosocial mode will not be discussed. The intervention group will receive a PNE lecture. All primary and secondary outcome measures consist of validated questionnaires (e.g., RNPQ, HC-PAIRS), except for the study-specific red-flags knowledge test; the study-specific case vignette assessing guideline-concordant low back pain recommendations underwent validation testing before participant recruitment.

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Conditions studied

  • Healthy Subjects

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Keywords

  • Pain
  • Physiotherapy students
  • Attitudes
  • Education
  • Pain Neuroscience Education (PNE)
  • The Revised Neurophysiology of Pain Questionnaire (RNPQ)
  • The 13-item Modified Health Care Providers Pain and Impairment Relationship Scale (HC-PAIRS)
  • Guideline-Concordant Low Back Pain Vignette (GCLBP-V)
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In context

Pain

10,054 studies on the registry are indexed under Pain; 1,649 are open to participants now.

This study's enrollment of 120 is above the median of 66 across 8,493 interventional studies indexed under Pain.

Browse Pain studies →

Lead sponsor

The Hashemite University is the lead sponsor of 9 studies on the registry; 2 are open to participants now.

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

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
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

  • Physiotherapy undergraduate students at the Hashemite University

Exclusion criteria

Exclusion Criteria:

  • Previous formal pain education
  • Enrolled in a clinical practice module
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Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
120 participants (actual)

Study arms

  • Experimental
    Pain Neuroscience Education

    Other: Pain Neuroscience Education

  • Active comparator
    Red Flags Education

Interventions

  • OtherPain Neuroscience Education

    The intervention group will receive a lecture of 70min duration on pain neuroscience. The objective of this educational session is to educate students that pain can be overprotective, and that nociceptive transmission can be heavily influenced by central sensitisation (sensitivity of the central nervous system) as well as the thoughts and beliefs of the individual. The session used drawings, stories and metaphors to depict the underlying neuroscience of pain, and current pain theory.

  • OtherRed Flags Education

    The control group received an education session of red flags. Red flags form part of routine subjective practice for therapists as a process of screening serious or potentially sinister pathologies. Sign and symptoms for such pathologies include history of cancer, systemic symptoms such as fever or unexplained weight loss, and saddle analgesia. The red flag session will not include the neuroscience of pain.

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What researchers measure

Primary outcomes

  1. Revised Pain Neurophysiology Questionnaire (RNPQ)

    The 12-item RNPQ will be used to assess knowledge of pain neurophysiology. Responses are marked yes, no or undecided. One point is awarded for correct answers. Scores range from 0 to 12, with high scores indicating good knowledge.

    Time frame: Before and immediately after and 6 months after the education session

  2. The modified HC-PAIRS

    The modified HC-PAIRS (Health Care Providers' Pain and Impairment Relationship Scale will be used to measure attitudes and beliefs towards patients with chronic pain and their ability to function. This 13-item questionnaire uses a 7-point Likert scale (strongly disagree to strongly agree). Scores range from 13 to 91 with lower scores suggesting more positive attitudes.

    Time frame: Prior to and immediately and 6 months after the education session

Secondary outcomes

  1. Guideline-concordant low back pain recommendations assessed using a case vignette

    A case vignette will be used to assess participants' vignette-based clinical recommendations for a patient with non-specific low back pain. Participants will answer four multiple-choice questions addressing recommendations regarding usual daily activities, work, exercise, and bed rest. Each domain will be scored as guideline-concordant or non-guideline-concordant according to contemporary low back pain guideline recommendations. The total number of guideline-concordant recommendations will be calculated, with possible scores ranging from 0 to 4; higher scores indicate more guideline-concordant recommendations. The percentage of guideline-concordant recommendations may also be reported. The vignette was developed for this study and psychometrically evaluated before participant recruitment and before its use as a trial outcome, including expert review for content validity, cognitive pretesting, construct validity assessment, test-retest reliability, and measurement error analysis.

    Time frame: Baseline, immediately after the education session, and 6 months after the education session.

Other outcomes

  1. LBP Red-Flags Knowledge Quiz (10-item)

    It is a 10-item quiz, with yes/no answers that assesses knowledge of red-flags. Scores range from 0 to 10. This questionnaire was developed within our team. This is to provide attention-matched control content and to support participant blinding to the vignette outcome. This tool is developed de novo to provide attention-matched control content and to evaluate knowledge of red-flag indicators of serious spinal pathology. This is a de novo instrument developed and face validated for this trial. The face validation process, conducted prior to participant recruitment.

    Time frame: Baseline, Post, and 6 months after lecture control session

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Study locations

1 site
  • The Hashemite University
    Zarqa, Zarqa Governorate 13133, Jordan
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References and documents

Publications

  • Colleary G, O'Sullivan K, Griffin D, Ryan CG, Martin DJ. Effect of pain neurophysiology education on physiotherapy students' understanding of chronic pain, clinical recommendations and attitudes towards people with chronic pain: a randomised controlled trial. Physiotherapy. 2017 Dec;103(4):423-429. doi: 10.1016/j.physio.2017.01.006. Epub 2017 Mar 22. PubMed 28797666 ↗

Individual participant data

Plan to share: Yes — After completion of the data collection, it will be analysed and then interpreted. I will provide you with the study results and recommendations upon completion.

Supporting information: Statistical analysis plan

Time frame: After being published, the dataset and/or the statistical analyses will be made available for interested researchers upon reasonable request.

Access criteria: After being published, the dataset and/or the statistical analyses will be made available for interested researchers upon reasonable request.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 15, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06821022
Lead sponsor
The Hashemite University
Responsible party
Ahmad Muhsen (Assistant Professor, The Hashemite University) — Principal investigator
First posted
Feb 11, 2025
Start date
Feb 15, 2024
Primary completion
May 13, 2026
Completion
May 13, 2026
Last update
May 15, 2026

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 May 2026. You cannot join it, but the record below documents what was studied.

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