Ignite Creation Date:
2024-06-16 @ 11:49 AM
Last Modification Date:
2024-10-26 @ 3:30 PM
Study NCT ID:
NCT06430281
Status:
RECRUITING
Last Update Posted:
2024-05-29
First Post:
2024-05-21
Brief Title:
Manual Therapy Force Perception Scale
Sponsor:
Université du Québec à Trois-Rivières
Organization:
Université du Québec à Trois-Rivières
Study Overview
Official Title:
Development and Pre-testing of a Manual Therapy Force Perception Scale
Status:
RECRUITING
Status Verified Date:
2024-05
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
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
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
Detailed Description:
The aim of this observational study is to pilot test an ordinal scale the Manual Therapy Force Perception MTFP scale intended to enable clinicians to assign ordinal rankings to their patients based on their perception of the force they applied during manual therapy This involved evaluating the agreement between the force applied by clinicians during spinal manipulations and mobilizations delivered on a manikin and their subjective perception of force as determined using the MTFP scale Additionally the pilot study aimed to seek feedback on the MTFP scale from clinicians who are its potential users
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None