- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06432946
Sensing-glove System in Manual Therapy
Effect of Two Facilitating Interventions on the Acceptability and Usability Towards a Sensing-glove System to Measure Force-time Characteristics of Spinal Manipulative Therapy: a Mixed-methods Cross-over Study
The objective of this clinical trial is to assess manual therapists' attitudes towards using a sensing-glove system for measuring spinal manipulation force and to compare the effectiveness of two interventions in enhancing their attitudes. The primary questions it aims to address are:
- Are manual therapists receptive to employing a sensing-glove system to measure the force applied during spinal manipulations on patients?
- Can we enhance manual therapists' attitudes towards this system through either a brief informational video demonstration or a supervised practice session with the system?
Researchers will compare the impact of a 7-minute informational video to that of a 20-minute supervised practice session to determine if manual therapists' attitudes towards the use of a sensing-glove while treating their patients can be positively influenced.
Participants will:
- Engage in a single experimental session.
- Complete a questionnaire at the beginning of the experimental session.
- Undergo one of the two interventions and promptly complete two questionnaires following this intervention.
- Undergo the other intervention and promptly complete the same two questionnaires following this intervention.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Quebec
-
Trois-Rivières, Quebec, Canada, G8Z 4M3
- Université du Québec à Trois-Rivières
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Being a licensed chiropractor or a last-year intern in a University outpatient chiropractic clinic
Exclusion Criteria:
- Reported any upper limb injury preventing them from executing manual therapies during the time of the study
- Previous experience with the sensing-glove system
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Video followed by practice
Participants will initially view a 7-minute informational video followed by a 20-minute supervised practice session with the sensing-glove system.
Acceptability and usability perception will be assessed after each intervention.
|
A 7-minute video demonstrating the sensing-glove system, how it can be used to assess manual therapy biomechanics, and its relevance in research and clinical contexts.
The video was created by the research team via a voiceover PowerPoint presentation.
A 20-minute practice session during which participants received verbal information about the sensing-glove system.
While wearing the sensing glove, participants performed palpation and manual therapy techniques (palpation, spinal mobilization/manipulation to the cervical and thoracic spine) on a human-sized manikin, guided by the researcher.
|
|
Experimental: Practice followed by video
Participants will initially participate in a 20-minute supervised practice session with the sensing-glove system followed by viewing a 7-minute informational video.
Acceptability and usability perception will be assessed after each intervention.
|
A 7-minute video demonstrating the sensing-glove system, how it can be used to assess manual therapy biomechanics, and its relevance in research and clinical contexts.
The video was created by the research team via a voiceover PowerPoint presentation.
A 20-minute practice session during which participants received verbal information about the sensing-glove system.
While wearing the sensing glove, participants performed palpation and manual therapy techniques (palpation, spinal mobilization/manipulation to the cervical and thoracic spine) on a human-sized manikin, guided by the researcher.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Acceptability
Time Frame: Immediately following each intervention and at baseline
|
French version of the questionnaire based on the extended version of the Unified Theory of Acceptance and Use of Technology (UTAUT2).
A higher score indicates a higher level of acceptability.
|
Immediately following each intervention and at baseline
|
|
Usability
Time Frame: Immediately following each intervention
|
French version of the System usability scale (F-SUS).
A higher score indicates a higher level of usability.
|
Immediately following each intervention
|
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_Acceptabilite_2021
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
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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