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Completed

NCT Number: NCT07051460

Study of the Effect of Proprioceptive Stimuli in the Stomatognathic Area on Visual Perception, With and Without Sound

The goal of this observational study is to investigate how oral proprioceptive stimuli affect visual perception and auditory-visual integration in healthy young adults. The main questions it aims to answer are:

* Can Oral Proprioceptive Stimuli (OPS) induce Visual pseudo-Scotomas (VS) in the absence of other stimuli? * Can Oral Proprioceptive Stimuli (OPS) modulate or eliminate Visual pseudo-Scotomas (VS) induced by auditory stimuli?

Researchers evaluated 38 healthy adults (aged 20-29) using the Vertical Maddox Test to detect functional visual alterations under different conditions. The study included four phases:

* Baseline assessment with no stimuli. * Assessment with auditory stimuli alone. * Assessment with simultaneous auditory and Oral Proprioceptive Stimuli (OPS), including tongue/lip positions (Combined Oral Stimuli) and dental pressure/traction stimuli (Dental Stimuli). * Assessment with Oral Proprioceptive Stimuli (OPS) alone.

Visual pseudo-scotomas were recorded based on participant responses. The study was approved by the local ethics committee and all participants gave informed consent.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Hospital Odontológico Universitat de Barcelona

Barcelona, Spain

About this study

Proprioception plays a well-established role in postural control and motor coordination, but increasing evidence supports its involvement in higher-level sensory processing, including spatial localization and multisensory integration. Given the anatomical overlap of trigeminal afferents innervating both oculomotor and orofacial structures, this study focused on the potential interplay between the stomatognathic and visual systems.

This study is an observational investigation with an experimental within-subject design with repeated measures in healthy volunteers.

The aim is to investigate the influence of oral proprioceptive stimuli on visual perception and audiovisual integration in healthy young adults, and explore whether non-invasive oral stimuli could modulate the occurrence of transient visual distortions-specifically Visual pseudo-Scotomas (VS)-when binocular vision is altered, and whether these stimuli could counteract the effects induced by auditory input.

Participants have been screened to ensure normal hearing, vision, and dental status, and underwent testing using the Vertical Maddox Test, which induces a dissociation in binocular vision that relies heavily on proprioceptive cues.

The experimental protocol was composed of four phases:

  • Baseline evaluation with no stimuli.
  • Application of auditory stimuli (500 Hz tones delivered through headphones) to assess their influence on visual perception.
  • Application of simultaneous auditory and Oral Proprioceptive Stimuli (OPS), including both Combined Oral Stimuli (COS, such as specific tongue and lip positions) and Dental Stimuli (DS, consisting of gentle pressure/traction on central incisors using a calibrated probe).
  • Application of Oral Proprioceptive Stimuli (OPS) alone, without sound.

Participants were asked to report the occurrence and location of any Visual pseudo-Scotomas (VS) observed during each phase. These were defined as functional visual field losses detected via the Vertical Maddox Test, with no underlying ocular pathology.

This protocol was developed based on prior work investigating ocular and oral proprioception and its role in multisensory integration. No pharmacological agents, devices, or therapeutic interventions were used. The study is observational in nature, and no biospecimens were collected or retained.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Exclusion criteria

  • General criteria:
  • Treatment with psychotropic drugs
  • Hearing loss in one or both ears
  • Visual criteria:
  • Visual acuity worse than 20/20 in one or both eyes
  • Stereopsis (three-dimensional vision) less than 120 arc sec
  • Vertical phoria greater than 0.75 Δ
  • Strabismus operated on or not
  • Ongoing optometric rehabilitation
  • History of amblyopia
  • Dental criteria:
  • Missing one or more incisors
  • Presence of conservative, prosthetic or orthodontic treatment on one or more incisors (fillings, root canal treatments, veneers, crowns, brackets, Invisalign type attachments...).

Treatment and study plan

Baseline Condition (No Stimuli)

Other

Participants underwent baseline evaluation using the Vertical Maddox Test with no auditory or oral proprioceptive stimulation. This phase was used to confirm the absence of spontaneous visual pseudo-scotomas and served as an internal control condition for each participant.

Other names: Phase 1

Auditory Stimulation only

Other

Participants received bilateral auditory stimulation consisting of 500 Hz tones (500 ms duration, 50 dB) delivered through wireless headphones, without any accompanying oral stimuli. This condition was used to assess the isolated effect of sound on visual perception using the Vertical Maddox Test.

Other names: Phase 2

Auditory and Oral Proprioceptive Stimulation (OPS)

Other

Participants received simultaneous auditory and oral proprioceptive stimuli while undergoing the Vertical Maddox Test. - Auditory: 500 Hz tones (500 ms, 50 dB) via headphones. - Oral Proprioceptive Stimuli (OPS): included Combined Oral Stimuli (e.g., tongue and lip self-administered positions) and Dental Stimuli (mechanical pressure or traction on central incisors using a calibrated probe). This condition aimed to assess whether OPS could modulate or eliminate sound-induced visual pseudo-scotomas.

Other names: Phase 3

Oral Proprioceptive Stimulation Only (OPS)

Other

Participants received oral proprioceptive stimuli alone, without auditory input, during the Vertical Maddox Test. - Combined Oral Stimuli (COS): self-administered tongue/lip positions. - Dental Stimuli (DS): applied by the operator to central incisors. This condition was used to evaluate the independent effect of OPS on visual perception.

Primary outcomes

  1. Presence of Visual Pseudo-Scotomas (VS) under Auditory and/or Oral Proprioceptive Stimulation

    Time frame: During 4-phase experimental protocol (single visit, approx. 45 minutes)

    Participants were assessed for the occurrence of functional visual disturbances (pseudo-scotomas, or VS) during each phase of the protocol using the Vertical Maddox Test. Presence or absence of VS was recorded under three experimental conditions: auditory stimulation alone, combined auditory and oral proprioceptive stimulation, and oral proprioceptive stimulation alone.

Secondary outcomes

  1. Elimination of Sound-Induced Visual Pseudo-Scotomas by Oral Proprioceptive Stimuli

    Time frame: Day 1, during phase 3 (auditory + OPS) of the experimental protocol

    Among participants who experienced VS during auditory stimulation alone, the presence or absence of VS was re-assessed during the combined application of auditory and oral proprioceptive stimuli to determine whether OPS could eliminate sound-induced visual disturbances.

  2. Presence of Visual Pseudo-Scotomas with Oral Proprioceptive Stimulation Alone

    Time frame: Day 1, during phase 4 (OPS alone) of the experimental protocol

    Participants were evaluated for the occurrence of visual pseudo-scotomas under oral proprioceptive stimuli without auditory input, to assess whether OPS alone could induce transient changes in visual perception.

Sponsors and collaborators

Lead sponsor

Sophie Román Richon

Other

Collaborators

  • Hospital Odontològic UB

Registry information

Official study title

MULTISENSORIALIDAD Y BOCA Estudio Del Efecto de estímulos Propioceptivos en el área estomatognática Sobre la percepción Visual, Con y Sin Sonido

Important dates

Study start
2022
Primary completion
2023
Study completion
2023
First posted
Jul 4, 2025
Registry last updated
Jul 4, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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