Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
ID06845969

Reducing Dangerous Placement of Needles by Physiotherapists Using Dry Needling Through Cadaver Anatomy Review: A Randomized Controlled Trial Assessing Needle Placement Accuracy and Confidence

Led by University of Alberta · Updated on 2026-05-06

60

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating whether adding cadaver anatomy review improves the accuracy and perceived safety of physiotherapists practicing dry needling. This study compares an anatomy review using cadaver materials to an educational session unrelated to anatomy. The aim is to see if the anatomy review enhances needle placement accuracy and safety compared to the control education. The study involves physiotherapists licensed in dry needling and needling participants experienced with receiving such treatments. The trial includes two groups: one receives a two-hour interactive cadaver anatomy review focused on high-risk areas, and the other attends a two-hour online education session about dry needling theory without anatomy content. Participants first complete baseline exams and needle three selected muscles using ultrasound to measure accuracy and safety. After the interventions, they retake knowledge exams and repeat the needling assessments within two weeks. During the study, therapists' needle placement is evaluated using ultrasound imaging on male and female needling volunteers to ensure safety and accuracy. Self-confidence in needling is also measured using a visual scale. The study measures changes in dry needling accuracy, safety, confidence, and anatomy knowledge before and after the interventions. Safety precautions and blinded assessments are in place to ensure reliable and unbiased results.

CONDITIONS

Brief Title

Physiotherapy Dry Needling Accuracy

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Licensed physiotherapists in good standing with their regulatory College who are authorized to practice dry needling.
  • Physiotherapists who have not taken a cadaver anatomy review class after their entry-to-practice physiotherapy program.
  • Needling volunteers who can provide informed consent.
Not Eligible

You will not qualify if you...

  • Physiotherapists not in good standing with their regulatory College or not authorized to practice dry needling.
  • Physiotherapists who have taken a cadaver anatomy review class after their physiotherapy program.
  • Needling volunteers with contraindications to dry needling or outside normal BMI measurements.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Baseline Assessments

Duration - Up to 1 week before intervention

Participants complete a baseline survey and an initial online anatomy knowledge exam. Dry needling accuracy and self-confidence are assessed using ultrasound imaging and a visual analogue scale on two separate needling volunteers.

1 baseline visit (in-person) and online assessments

Intervention

Duration - 1 day

Participants receive either a two-hour interactive cadaver anatomy review class focused on high-risk areas or a two-hour online dry needling theory education session.

1 education session (in-person for cadaver group, online for theory group)

Post-Intervention Assessments

Duration - Within 2 weeks after intervention

Within 24 hours after the intervention, participants complete a second online anatomy knowledge exam and self-confidence assessment. Within two weeks, dry needling accuracy is reassessed using ultrasound imaging on different needling volunteers.

1 online exam and confidence assessment; 1 follow-up visit (in-person) for ultrasound assessment

Trial Site Locations

Total: 1 location

1

University of Alberta

Edmonton, Alberta, Canada, T6G2B7

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Research Team

N

Nadine R Crocker, MScPT

E

Eric Parent, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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