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Sensing-glove System in Manual Therapy

Not Applicable
Completed
Conditions
Spinal Manipulation
Interventions
Other: Video
Other: Practice session
Registration Number
NCT06432946
Lead Sponsor
Université du Québec à Trois-Rivières
Brief Summary

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.

Detailed Description

This study aimed to evaluate manual therapists' acceptability of a sensing-glove system for measuring spinal manipulation's force-time characteristics and compare the effectiveness of two interventions in enhancing their acceptability and usability perception. Participants will undergo two acceptability-enhancing interventions in randomized order: a 7-minute informational video and a 20-minute supervised practice session. At the start of the session and after each intervention, the acceptability and perception of usability towards the system will be assessed.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
16
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 & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Video followed by practicePractice sessionParticipants 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.
Video followed by practiceVideoParticipants 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.
Practice followed by videoVideoParticipants 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.
Practice followed by videoPractice sessionParticipants 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.
Primary Outcome Measures
NameTimeMethod
AcceptabilityImmediately 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.

UsabilityImmediately following each intervention

French version of the System usability scale (F-SUS). A higher score indicates a higher level of usability.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Université du Québec à Trois-Rivières

🇨🇦

Trois-Rivières, Quebec, Canada

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