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Oral Proprioceptive Sensitivity and Upper Limb Kinesthetic AcuityNCT07854314

Oral Proprioceptive Sensitivity and Upper Limb Kinesthetic Acuity: A Pilot Study

An observational study of Oral Proprioceptive Sensitivity and Upper Limb Kinesthetic Acuity, run by Sophie Román Richon at 1 site in Spain.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The goal of this observational study is to investigate whether differences in oral proprioceptive sensitivity are associated with differences in kinesthetic acuity of the upper limbs in children. Read more about this study

Who is it for?
Ages Up to 15 yearsHealthy volunteers can take part
What is being tested?
Upper-Limb Kinesthetic Acuity Assessment, Effect of Auditory Stimulation on Visual Perception and Oral Proprioceptive Sensitivity Assessment
Type of treatment
Pill or oral medicine
How many people
33 participants
Where
1 siteSpain
Study dates
14 Jan 2024to 14 Dec 2024
How long will I take part?
1 Day
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Up to 15 years
  • All sexes
  • Healthy volunteers accepted
  • Child

Study population: The study population consists of children younger than 15 years who have all eight permanent incisors and who meet the study eligibility criteria. Participants are recruited among patients of the Hospital Odontològic Universitat de Barcelona (HOUB) and children accompanying their parents or relatives attending the HOUB. The study includes children without neurological, sensory, motor, auditory, visual, or dental conditions that could interfere with the study procedures or the interpretation of the results.

Who may be able to join

  • Children younger than 15 years.
  • Presence of all eight permanent incisors.
  • Voluntary agreement to participate in the study.

Who cannot join

  • Neurological, sensory, or motor conditions that could interfere with the performance or interpretation of the study procedures.
  • Treatment with psychotropic medication.
  • Hearing loss in one or both ears.
  • Visual acuity below 20/20 in either eye.
  • Stereoacuity below 120 arc seconds.
  • Vertical phoria greater than 0.75 prism diopters.
Show all 10Show fewer
  • Strabismus, whether previously operated or not.
  • Ongoing optometric rehabilitation.
  • History of amblyopia.
  • Absence of one or more permanent incisors.

Trial locations and contacts

1 site in 1 country.

Spain1 site
  • Hospital Odontològic UB

    L'Hospitalet de Llobregat, Barcelona, 08907

Other trials in Spain

About this study

Official title: Possible Correlation Between Variability in Oral Proprioceptive Sensitivity and Variability in Upper Limb Kinesthetic Acuity

The goal of this observational study is to investigate whether differences in oral proprioceptive sensitivity are associated with differences in kinesthetic acuity of the upper limbs in children.

The study examines two aspects of proprioception: oral proprioceptive sensitivity, which refers to the sensory response to proprioceptive stimulation of structures in the mouth, and upper-limb kinesthetic acuity, which refers to the ability to perceive the position or movement of the arms without relying on vision.

Read more

The study will also explore whether oral and auditory sensory stimuli can produce small, transient visual losses, referred to as visual pseudoscotomas, during a perceptual test based on the Maddox rod. Participants will complete standardized experimental tasks designed to assess upper-limb kinesthetic acuity and oral proprioceptive sensitivity.

The study is intended to contribute to the understanding of possible relationships between oral proprioception and proprioception of the upper limbs in children, and of how oral and auditory sensory information may interact with visual perception.

Read the detailed description

This observational, descriptive, cross-sectional study investigates the possible relationship between oral proprioceptive sensitivity and kinesthetic acuity of the upper limbs in children younger than 15 years.

The study consists of two main assessments:

Upper-Limb Kinesthetic Acuity

Upper-limb kinesthetic acuity is assessed using a matching task based on the method described by Proske and Gandevia. With their eyes covered, participants reproduce the position of one forearm with the other. The angular position of both forearms is measured using digital inclinometers, and the difference between the reference and indicator arms is recorded across repeated trials. The procedure is performed five times for forearm flexion and five times for extension.

Oral Proprioceptive Sensitivity and Visual Perception

The effect of oral proprioceptive stimulation on visual perception is assessed using the Perceptive Maddox Test. Participants lie on a rigid examination table, with the head position maintained by the examiner. The test produces binocular dissociation, allowing the participant to perceive a horizontal red line and a point of light as separate visual images.

The assessment is performed in three phases. First, participants are exposed to auditory stimulation alone, consisting of five 10-second sequences of simultaneous 500-Hz whistles presented to both ears at approximately 50 dB. The occurrence and characteristics of transient visual losses (visual pseudoscotomas) are recorded.

Second, auditory stimulation is combined with different oral proprioceptive stimuli involving the incisors, including tongue contact and examiner-applied pressure. The effect of these stimuli on the visual perception of the red line is recorded.

Third, calibrated pressure or traction stimuli are applied to the incisors using a dynamometer, according to the oral stimulus that produced a visual effect in the previous phase. The temporal and spatial characteristics of the response, as well as the variability in the pressure or traction required, are recorded.

The study is exploratory and aims to characterize the possible relationship between oral proprioceptive responses and upper-limb kinesthetic acuity, as well as the interaction between oral and auditory sensory stimulation and visual perception.

Being tested
Upper-Limb Kinesthetic Acuity Assessment, Effect of Auditory Stimulation on Visual Perception, Oral Proprioceptive Sensitivity Assessment
Keywords
Oral proprioceptive sensitivity, Proprioception, Kinesthetic acuity, Transient visual loss, Multisensory integration
Medical subject headings
Blindness

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Upper-Limb Kinesthetic Acuity AssessmentOther

    Also called Phase 1, Kinesthetic Matching Task

    Participants performed a matching task with both forearms while their eyes were covered. One forearm was positioned by the examiner at a predetermined angle, and the participant moved the other forearm to match its perceived position. The angular position of both forearms was measured using digital inclinometers. The procedure was repeated five times for forearm flexion and five times for extension to assess the variability of upper-limb kinesthetic acuity.

  • Effect of Auditory Stimulation on Visual PerceptionOther

    Also called Phase 2, Perceptive Maddox Test and Auditory Stimulation

    Participants underwent the Perceptive Maddox Test while receiving bilateral auditory stimulation consisting of simultaneous 500-Hz whistles presented through wireless headphones at approximately 50 dB. Five 10-second sequences were presented. Participants reported whether the red line disappeared completely or partially and, when applicable, indicated the location and changes in location of the visual loss. The occurrence and temporal and spatial characteristics of transient visual losses (visual pseudoscotomas) were recorded.

  • Oral Proprioceptive Sensitivity AssessmentOther

    Also called Phase 3, Perceptive Maddox Test and Oral Proprioceptive Stimulation

    The effect of oral proprioceptive stimulation on visual perception was assessed using the Perceptive Maddox Test in combination with auditory stimulation. Oral stimuli consisted of examiner-applied pressure to the vestibular surfaces of the incisors. When an oral stimulus produced a visual effect, calibrated pressure or traction was applied to the incisors using a dynamometer. The temporal and spatial characteristics of the visual response and the variability in the pressure or traction required were recorded.

Study groups in NCT07854314
Study groupRoleWhat they receive
Children younger than 15 yearsChildren younger than 15 years who participate in the study and undergo assessments of upper-limb kinesthetic acuity and the effect of oral proprioceptive stimulation on visual perception.
Receives: Other: Upper-Limb Kinesthetic Acuity Assessment; Other: Effect of Auditory Stimulation on Visual Perception; Other: Oral Proprioceptive Sensitivity Assessment

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Correlation between upper-limb kinesthetic acuity and oral proprioceptive sensitivity

    Correlation between variability in upper-limb kinesthetic acuity, assessed by the matching task, and variability in the visual response to oral proprioceptive stimulation during the Perceptive Maddox Test.

    Measured: Day 1

Secondary outcomes (3)
  1. Occurrence of auditory-induced visual pseudoscotomas

    Proportion of participants who experience transient visual losses (visual pseudoscotomas) during bilateral auditory stimulation in the Perceptive Maddox Test.

    Measured: Day 1

  2. Effect of oral proprioceptive stimulation on auditory-induced visual pseudoscotomas

    Proportion of participants in whom oral proprioceptive stimulation suppresses auditory-induced visual pseudoscotomas, and characterization of the oral stimuli producing this effect.

    Measured: Day 1

  3. Lability of the visual response to oral proprioceptive stimulation

    Temporal and spatial lability of the visual response to oral proprioceptive stimulation and variability in the pressure or traction intensity required to suppress visual pseudoscotomas.

    Measured: Day 1

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted2 Oct 2026
  2. Study start14 Jan 2024
  3. Primary completion14 Dec 2024
  4. Study completion14 Dec 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Cross-sectional
Enrolment
33 participants (actual)
Target duration
1 Day
IDs, dates and publications
ClinicalTrials.gov ID
NCT07854314
Sponsor's protocol ID
CEIm HOUB 27/2023
Status last verified
Sep 2026
First submitted
22 Sep 2026
Last updated
2 Oct 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

An observational study of Oral Proprioceptive Sensitivity and Upper Limb Kinesthetic Acuity, run by Sophie Román Richon at 1 site in Spain.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 10 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 2 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Spain. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Correlation between upper-limb kinesthetic acuity and oral proprioceptive sensitivity (time frame: Day 1). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Oct 2026.

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