- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06430281
Manual Therapy Force Perception Scale
Development and Pre-testing of a Manual Therapy Force Perception Scale
The objective of this observational study is to pilot a scale designed to assist clinicians in evaluating the force they perceive during manual therapy.
The main question it aims to answer is:
- Are clinicians able to evaluate the force they use when delivering manual therapies to their patients using a scale?
For the pilot test, licensed chiropractors administer manual therapies on a manikin.
Study Overview
Detailed Description
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Quebec
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Trois-Rivières, Quebec, Canada, G8Z 4M3
- Université du Québec à Trois-Rivières
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Licensed chiropractors with a private practice within the province of Quebec, Canada.
Exclusion Criteria:
- Having a condition that prevents the execution of approximately 50 manual therapies over a 1-hour period.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Participants
Chiropractors will administer manual therapies on a manikin utilizing three distinct levels of force (typical force, low force, high force), determined by the trial label on the scale.
A sensor will gauge the magnitude of force applied.
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A manual force will be applied to a manikin positioned on a chiropractic treatment table.
The force exerted during the manual therapy must align with the trial label indicated on the Manual Therapy Force Perception [MTFP] scale.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Peak force measured by a force sensor during the manual therapy
Time Frame: During the manual therapy
|
The therapy will be delivered on a force sensor (Loadpad(R)) which will measured the force applied.
The peak force reached during the therapy will be extracted.
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During the manual therapy
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Collaborators and Investigators
Investigators
- Principal Investigator: Isabelle Pagé, DC, PhD, Université du Québec à Trois-Rivières
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
Other Study ID Numbers
- UQTR_IP_EchelleTM_2024
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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