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Dry Needling for Physical Therapy

Edmonton, Canada
N/A
Waitlist Available
Led By Eric Parent, PhD
Research Sponsored by University of Alberta
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Must not have
Needling volunteers who possess any contraindications to dry needling or are not within normal BMI measurements
Timeline
Screening 3 weeks
Treatment Varies
Follow Up this measurement will be taken initially when the subject enrolls in the study (baseline) and again within two weeks of having received the intervention (either control or experimental) (follow-up).

Summary

This trial aims to see if reviewing anatomy using cadaver materials can improve the accuracy and safety of physiotherapists who practice dry needling. Participants will needle three muscles, take a knowledge exam

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Who is the study for?
This trial is for physiotherapists who practice dry needling. Participants should be willing to undergo educational sessions and demonstrate their needling skills on three specific muscles using ultrasound imaging. There are no specific inclusion or exclusion criteria provided.Check my eligibility
What is being tested?
The study aims to determine if a cadaver anatomy review class can improve the accuracy and perceived safety of dry needling by physiotherapists, compared to a control group receiving unrelated online education.See study design
What are the potential side effects?
Since this trial focuses on educational interventions rather than medical treatments, traditional side effects are not applicable. However, participants may experience discomfort associated with learning new techniques.

Eligibility Criteria

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
Select...
I do not have conditions that prevent dry needling and my BMI is normal.
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Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~this measurement will be taken initially when the subject enrolls in the study (baseline) and again within two weeks of having received the intervention (either control or experimental) (follow-up).
This trial's timeline: 3 weeks for screening, Varies for treatment, and this measurement will be taken initially when the subject enrolls in the study (baseline) and again within two weeks of having received the intervention (either control or experimental) (follow-up). for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Dry needling accuracy
Secondary study objectives
Dry needling safety
Knowledge exam score (Dry Needling)
Knowledge exam score (anatomy)
+1 more

Trial Design

2Treatment groups
Experimental Treatment
Placebo Group
Group I: Education: Cadaver anatomy reviewExperimental Treatment1 Intervention
A two hour cadaver lab review course focused on high risk areas for dry needling.
Group II: Education: dry needling theoryPlacebo Group1 Intervention
A two hour on-line synchronous educational model focused on dry needling theory.

Find a Location

Closest Location:University of Alberta· Edmonton, Canada

Who is running the clinical trial?

University of AlbertaLead Sponsor
954 Previous Clinical Trials
436,081 Total Patients Enrolled
Eric Parent, PhDPrincipal InvestigatorUniversity of Alberta
~40 spots leftby Aug 2026