CClinicalTrials.gg
CompletedNCT06432946Updated Mar 30, 2025

Sensing-glove System in Manual Therapy

An interventional study of Video and Practice session in Spinal Manipulation, sponsored by Université du Québec à Trois-Rivières. Completed at 1 site in Canada. Per ClinicalTrials.gov, last updated 2025-03-30.

Sponsored by Université du Québec à Trois-Rivières · Not applicable, Interventional, and Other

From the registry’s dates

  • Registered 2 years 11 months after the study started (first participant enrolled Jun 2021, registered May 2024).
Phase
Not applicable
Study type
Interventional
Enrollment
16
Allocation
Randomized
Sex
All
01

Study 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.
Read the 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.

02

Conditions studied

  • Spinal Manipulation

Keywords

  • Chiropractic
  • Manual therapy
  • Acceptability
  • Usability
  • Force-time characteristics
03

In context

Lead sponsor

Université du Québec à Trois-Rivières is the lead sponsor of 40 studies on the registry; 8 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Being a licensed chiropractor or a last-year intern in a University outpatient chiropractic clinic

Exclusion criteria

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
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
16 participants (actual)

Study arms

  • 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.

    Other: Video · Other: Practice session

  • 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.

    Other: Video · Other: Practice session

Interventions

  • OtherVideo

    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.

  • OtherPractice session

    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.

06

What researchers measure

Primary outcomes

  1. Acceptability

    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.

    Time frame: Immediately following each intervention and at baseline

  2. Usability

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

    Time frame: Immediately following each intervention

07

Study locations

1 site
  • Université du Québec à Trois-Rivières
    Trois-Rivières, Quebec G8Z 4M3, Canada
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 30, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06432946
Lead sponsor
Université du Québec à Trois-Rivières
Responsible party
Isabelle Pagé (Professor, Université du Québec à Trois-Rivières) — Principal investigator
First posted
May 29, 2024
Start date
Jun 1, 2021
Primary completion
Aug 31, 2021
Completion
Aug 31, 2021
Last update
Mar 30, 2025

Study contacts

Isabelle Pagé, DC, PhD
principal investigator · Université du Québec à Trois-Rivières

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Mar 2025. You cannot join it, but the record below documents what was studied.

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