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Acute Effects of Oculomotor Exercises on Posturography and Gait Analysis Parameters in Regular Exercisers (OMEX-PG)

16 luglio 2026 aggiornato da: Vedat Kavak, Ege University

The Acute Effects of Oculomotor Exercises on Static Posturography and Gait Analysis Parameters in Regular Exercisers

This study aims to investigate the acute effects of a single-session oculomotor exercise program on static posturography and gait analysis parameters in healthy individuals who exercise regularly. Postural control and gait are complex sensorimotor functions that depend on the integration of visual, vestibular, somatosensory, and motor systems. Eye movements and gaze stabilization may contribute to postural orientation and locomotor control by influencing visual-vestibular integration, head-eye coordination, and sensorimotor adaptation. However, the immediate effects of short-duration oculomotor exercise programs on postural sway and gait-related parameters in regular exercisers have not been fully clarified.

This study is designed as a single-group, within-session, pre-post interventional study. Participants will undergo baseline assessments, complete a single session of oculomotor exercises, and then be reassessed after the intervention in the same testing session. The study population will consist of healthy adults who exercise regularly and meet the predefined eligibility criteria. Individuals with musculoskeletal injury, neurological or vestibular disorders, visual conditions that may affect balance or eye movement performance, or any condition limiting participation in the testing procedures will be excluded.

Static posturography will be performed using the HUR SmartBalance BTG4 system to evaluate postural sway under different sensory conditions. Measurements will be obtained during quiet standing with eyes open on a firm surface, eyes closed on a firm surface, eyes open on a foam surface, and eyes closed on a foam surface. The main posturography variables will include sway area, trace length, sway velocity, lateral sway, and anterior-posterior sway.

Gait analysis will be performed before and after the intervention using the DIERS Pedogait system. Spatiotemporal, phase-related, and center-of-pressure-based gait parameters will be recorded. These parameters may include step length, stride length, step time, stride time, track width, cadence, stance phase, swing phase, double support, pre-swing, and center-of-pressure-related gait variables.

The oculomotor exercise program will include three main components: extraocular eye movement exercises, vestibulo-ocular and cervico-ocular gaze stabilization exercises, and accommodation exercises. During extraocular eye movement exercises, participants will be asked to follow a visual target with eye movements while keeping the head stable. During gaze stabilization exercises, participants will maintain visual fixation on a target while performing controlled head movements and walking steps. During accommodation exercises, participants will alternate focus between a near target and a distant target. The exercises will be performed at different speeds to stimulate oculomotor control, gaze stabilization, and visual focusing mechanisms.

The primary outcome of the study is the change in sway area from baseline to the post-intervention assessment. Secondary outcomes include changes in other static posturography parameters and gait analysis variables. By evaluating both postural sway and gait-related outcomes, this study aims to provide preliminary evidence on whether a short oculomotor exercise session may produce immediate changes in postural control and walking characteristics in regular exercisers.

Panoramica dello studio

Tipo di studio

Interventistico

Iscrizione (Stimato)

51

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

    • Bornova
      • Izmir, Bornova, Turchia (Türkiye), 35100
        • Ege University Faculty of Medicine, Department of Sports Medicine

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto

Accetta volontari sani

Descrizione

Inclusion Criteria:

  • Healthy adults aged 18 to 50 years
  • Regular participation in exercise
  • Ability to walk independently without an assistive device
  • Ability to understand and follow the study procedures
  • Ability to complete the oculomotor exercise program, static posturography assessment, and gait analysis
  • Provision of written informed consent

Exclusion Criteria:

  • Acute musculoskeletal injury or pain that could affect balance, gait, or exercise performance
  • Neurological disease that could affect balance, gait, or oculomotor control
  • Vestibular disorder or current symptoms of dizziness or vertigo
  • Visual or ocular disorder that could affect visual fixation, eye movements, or balance assessment
  • Use of medication that could affect balance, coordination, alertness, or gait
  • Inability to walk independently
  • Inability to complete the oculomotor exercise intervention or assessment procedures
  • Any medical condition considered by the investigator to interfere with safe participation or the validity of the assessments

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Altro
  • Assegnazione: N / A
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Oculomotor Exercise Group
Participants in this single-arm group will receive a single-session oculomotor exercise program. Static posturography and gait analysis assessments will be performed before and after the intervention within the same testing session.
The intervention consists of a single-session oculomotor exercise program including extraocular eye movement exercises, vestibulo-ocular and cervico-ocular gaze stabilization exercises, and accommodation exercises. During extraocular eye movement exercises, participants will follow a visual target with eye movements while keeping the head stable. During gaze stabilization exercises, participants will maintain visual fixation on a target while performing controlled head movements and walking steps. During accommodation exercises, participants will alternate visual focus between a near target and a distant target. Exercises will be performed at different speeds within the same session.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change From Baseline in Sway Area Under Four Sensory Conditions
Lasso di tempo: Baseline and 15 minutes after the intervention
Sway area was assessed during 30 seconds of quiet standing using the HUR SmartBalance BTG4 static posturography system. Measurements were obtained under four sensory conditions: eyes open on a firm surface, eyes closed on a firm surface, eyes open on a foam surface, and eyes closed on a foam surface. Condition-specific sway area values were expressed using the same unit of measure (mm²). The change from baseline to 15 minutes after the single-session oculomotor exercise intervention was evaluated separately for each sensory condition..
Baseline and 15 minutes after the intervention

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change From Baseline in Trace Length Under Four Sensory Conditions
Lasso di tempo: Baseline and 15 minutes after the intervention
Trace length was assessed during 30 seconds of quiet standing using the HUR SmartBalance BTG4 static posturography system. Measurements were obtained under eyes-open firm-surface, eyes-closed firm-surface, eyes-open foam-surface, and eyes-closed foam-surface conditions. Condition-specific trace length values were expressed using the same unit of measure (mm). The change from baseline to 15 minutes after the intervention was evaluated separately for each sensory condition.
Baseline and 15 minutes after the intervention
Change From Baseline in Single-Support Phase Percentage
Lasso di tempo: Baseline and 15 minutes after the intervention
Right and left single-support phase values were assessed during barefoot treadmill walking at 3 km/h using the DIERS Pedogait system. Single support was expressed as a percentage of the gait cycle. The change from baseline to 15 minutes after the intervention was evaluated separately for each side.
Baseline and 15 minutes after the intervention
Change From Baseline in Sway Velocity Under Four Sensory Conditions
Lasso di tempo: Baseline and 15 minutes after the intervention
Sway velocity was assessed during 30 seconds of quiet standing using the HUR SmartBalance BTG4 static posturography system. Measurements were obtained under eyes-open firm-surface, eyes-closed firm-surface, eyes-open foam-surface, and eyes-closed foam-surface conditions. Condition-specific sway velocity values were expressed using the same unit of measure (mm/s) . The change from baseline to 15 minutes after the intervention was evaluated separately for each sensory condition.
Baseline and 15 minutes after the intervention
Change From Baseline in Mediolateral Sway Under Four Sensory Conditions
Lasso di tempo: Baseline and 15 minutes after the intervention
Mediolateral sway was assessed during 30 seconds of quiet standing using the HUR SmartBalance BTG4 static posturography system. Measurements were obtained under eyes-open firm-surface, eyes-closed firm-surface, eyes-open foam-surface, and eyes-closed foam-surface conditions. Condition-specific mediolateral sway values were expressed using the same unit of measure (mm). The change from baseline to 15 minutes after the intervention was evaluated separately for each sensory condition.
Baseline and 15 minutes after the intervention
Change From Baseline in Anteroposterior Sway Under Four Sensory Conditions
Lasso di tempo: Baseline and 15 minutes after the intervention
Anteroposterior sway was assessed during 30 seconds of quiet standing using the HUR SmartBalance BTG4 static posturography system. Measurements were obtained under eyes-open firm-surface, eyes-closed firm-surface, eyes-open foam-surface, and eyes-closed foam-surface conditions. Condition-specific anteroposterior sway values were expressed using the same unit of measure (mm). The change from baseline to 15 minutes after the intervention was evaluated separately for each sensory condition.
Baseline and 15 minutes after the intervention
Change From Baseline in Romberg Quotient on Firm and Foam Surfaces
Lasso di tempo: Baseline and 15 minutes after the intervention
The Romberg quotient was calculated using static posturography measurements obtained during eyes-open and eyes-closed standing. Separate Romberg quotient values were calculated for the firm and foam surfaces using the HUR SmartBalance BTG4 system. Both values were expressed using the same unit of measure. The change from baseline to 15 minutes after the intervention was evaluated separately for each surface.
Baseline and 15 minutes after the intervention
Change From Baseline in Step Length
Lasso di tempo: Time Frame: Baseline and 15 minutes after the intervention
Right and left step length values were assessed during barefoot treadmill walking at 3 km/h using the DIERS Pedogait system. Right and left values represented the same outcome variable and were expressed using the same unit of measure. The change from baseline to 15 minutes after the intervention was evaluated separately for each side.
Time Frame: Baseline and 15 minutes after the intervention
Change From Baseline in Track Width
Lasso di tempo: Baseline and 15 minutes after the intervention
Track width was assessed during barefoot treadmill walking at 3 km/h using the DIERS Pedogait system. Track width represents the mediolateral distance between consecutive foot placements. The change from baseline to 15 minutes after the intervention was evaluated.
Baseline and 15 minutes after the intervention
Change From Baseline in Stride Length
Lasso di tempo: Baseline and 15 minutes after the intervention
Right and left stride length values were assessed during barefoot treadmill walking at 3 km/h using the DIERS Pedogait system. Right and left values represented the same outcome variable and were expressed using the same unit of measure. The change from baseline to 15 minutes after the intervention was evaluated separately for each side.
Baseline and 15 minutes after the intervention
Change From Baseline in Step Time
Lasso di tempo: Baseline and 15 minutes after the intervention
Right and left step time values were assessed during barefoot treadmill walking at 3 km/h using the DIERS Pedogait system. Right and left values represented the same outcome variable and were expressed using the same unit of measure. The change from baseline to 15 minutes after the intervention was evaluated separately for each side.
Baseline and 15 minutes after the intervention
Change From Baseline in Stride Time
Lasso di tempo: Baseline and 15 minutes after the intervention
Right and left stride time values were assessed during barefoot treadmill walking at 3 km/h using the DIERS Pedogait system. Right and left values represented the same outcome variable and were expressed using the same unit of measure. The change from baseline to 15 minutes after the intervention was evaluated separately for each side.
Baseline and 15 minutes after the intervention
Change From Baseline in Stance Phase Percentage
Lasso di tempo: Baseline and 15 minutes after the intervention
Right and left stance phase values were assessed during barefoot treadmill walking at 3 km/h using the DIERS Pedogait system. Stance phase was expressed as a percentage of the gait cycle. The change from baseline to 15 minutes after the intervention was evaluated separately for each side.
Baseline and 15 minutes after the intervention
Change From Baseline in Pre-Swing Phase Percentage
Lasso di tempo: Baseline and 15 minutes after the intervention
Right and left pre-swing phase percentages were assessed during barefoot treadmill walking at 3 km/h using the DIERS Pedogait system. Pre-swing was expressed as a percentage of the gait cycle. The change from baseline to 15 minutes after the intervention was evaluated separately for each side.
Baseline and 15 minutes after the intervention
Change From Baseline in Double-Support Phase Percentage
Lasso di tempo: Baseline and 15 minutes after the intervention
Right and left double-support phase percentages were assessed during barefoot treadmill walking at 3 km/h using the DIERS Pedogait system. Double support was expressed as a percentage of the gait cycle. The change from baseline to 15 minutes after the intervention was evaluated separately for each side.
Baseline and 15 minutes after the intervention
Change From Baseline in Swing Phase Percentage
Lasso di tempo: Baseline and 15 minutes after the intervention
Right and left swing phase values were assessed during barefoot treadmill walking at 3 km/h using the DIERS Pedogait system. Swing phase was expressed as a percentage of the gait cycle. The change from baseline to 15 minutes after the intervention was evaluated separately for each side.
Baseline and 15 minutes after the intervention
Change From Baseline in Load Response Phase Percentage
Lasso di tempo: Baseline and 15 minutes after the intervention
Right and left load response phase values were assessed during barefoot treadmill walking at 3 km/h using the DIERS Pedogait system. Load response was expressed as a percentage of the gait cycle. The change from baseline to 15 minutes after the intervention was evaluated separately for each side.
Baseline and 15 minutes after the intervention
Change From Baseline in Single-Support Phase Percentage
Lasso di tempo: Baseline and 15 minutes after the intervention
Right and left single-support phase percentages were assessed during barefoot treadmill walking at 3 km/h using the DIERS Pedogait system. Single support was expressed as a percentage of the gait cycle. The change from baseline to 15 minutes after the intervention was evaluated separately for each side.
Baseline and 15 minutes after the intervention

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

2 settembre 2025

Completamento primario (Stimato)

5 settembre 2026

Completamento dello studio (Stimato)

11 novembre 2026

Date di iscrizione allo studio

Primo inviato

12 luglio 2026

Primo inviato che soddisfa i criteri di controllo qualità

16 luglio 2026

Primo Inserito (Effettivo)

21 luglio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

21 luglio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

16 luglio 2026

Ultimo verificato

1 luglio 2026

Maggiori informazioni

Termini relativi a questo studio

Termini MeSH pertinenti aggiuntivi

Altri numeri di identificazione dello studio

  • EUTF-OKULO-33058

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Descrizione del piano IPD

Individual participant data will not be shared due to institutional and ethical restrictions and because the informed consent process did not include permission for public sharing of individual-level data.

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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