Tämä sivu käännettiin automaattisesti, eikä käännösten tarkkuutta voida taata. Katso englanninkielinen versio lähdetekstiä varten.

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

torstai 16. heinäkuuta 2026 päivittänyt: 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.

Tutkimuksen yleiskatsaus

Opintotyyppi

Interventio

Ilmoittautuminen (Arvioitu)

51

Vaihe

  • Ei sovellettavissa

Yhteystiedot ja paikat

Tässä osiossa on tutkimuksen suorittajien yhteystiedot ja tiedot siitä, missä tämä tutkimus suoritetaan.

Opiskelupaikat

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

Osallistumiskriteerit

Tutkijat etsivät ihmisiä, jotka sopivat tiettyyn kuvaukseen, jota kutsutaan kelpoisuuskriteereiksi. Joitakin esimerkkejä näistä kriteereistä ovat henkilön yleinen terveydentila tai aiemmat hoidot.

Kelpoisuusvaatimukset

Opintokelpoiset iät

  • Aikuinen

Hyväksyy terveitä vapaaehtoisia

Joo

Kuvaus

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

Opintosuunnitelma

Tässä osiossa on tietoja tutkimussuunnitelmasta, mukaan lukien kuinka tutkimus on suunniteltu ja mitä tutkimuksella mitataan.

Miten tutkimus on suunniteltu?

Suunnittelun yksityiskohdat

  • Ensisijainen käyttötarkoitus: Muut
  • Jako: Ei käytössä
  • Inventiomalli: Yksittäinen ryhmätehtävä
  • Naamiointi: Ei mitään (avoin tarra)

Aseet ja interventiot

Osallistujaryhmä / Arm
Interventio / Hoito
Kokeellinen: 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.

Mitä tutkimuksessa mitataan?

Ensisijaiset tulostoimenpiteet

Tulosmittaus
Toimenpiteen kuvaus
Aikaikkuna
Change From Baseline in Sway Area Under Four Sensory Conditions
Aikaikkuna: 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

Toissijaiset tulostoimenpiteet

Tulosmittaus
Toimenpiteen kuvaus
Aikaikkuna
Change From Baseline in Trace Length Under Four Sensory Conditions
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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

Yhteistyökumppanit ja tutkijat

Täältä löydät tähän tutkimukseen osallistuvat ihmiset ja organisaatiot.

Sponsori

Opintojen ennätyspäivät

Nämä päivämäärät seuraavat ClinicalTrials.gov-sivustolle lähetettyjen tutkimustietueiden ja yhteenvetojen edistymistä. National Library of Medicine (NLM) tarkistaa tutkimustiedot ja raportoidut tulokset varmistaakseen, että ne täyttävät tietyt laadunvalvontastandardit, ennen kuin ne julkaistaan ​​julkisella verkkosivustolla.

Opi tärkeimmät päivämäärät

Opiskelun aloitus (Todellinen)

Tiistai 2. syyskuuta 2025

Ensisijainen valmistuminen (Arvioitu)

Lauantai 5. syyskuuta 2026

Opintojen valmistuminen (Arvioitu)

Keskiviikko 11. marraskuuta 2026

Opintoihin ilmoittautumispäivät

Ensimmäinen lähetetty

Sunnuntai 12. heinäkuuta 2026

Ensimmäinen toimitettu, joka täytti QC-kriteerit

Torstai 16. heinäkuuta 2026

Ensimmäinen Lähetetty (Todellinen)

Tiistai 21. heinäkuuta 2026

Tutkimustietojen päivitykset

Viimeisin päivitys julkaistu (Todellinen)

Tiistai 21. heinäkuuta 2026

Viimeisin lähetetty päivitys, joka täytti QC-kriteerit

Torstai 16. heinäkuuta 2026

Viimeksi vahvistettu

Keskiviikko 1. heinäkuuta 2026

Lisää tietoa

Tähän tutkimukseen liittyvät termit

Muita asiaankuuluvia MeSH-ehtoja

Muut tutkimustunnusnumerot

  • EUTF-OKULO-33058

Yksittäisten osallistujien tietojen suunnitelma (IPD)

Aiotko jakaa yksittäisten osallistujien tietoja (IPD)?

EI

IPD-suunnitelman kuvaus

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.

Lääke- ja laitetiedot, tutkimusasiakirjat

Tutkii yhdysvaltalaista FDA sääntelemää lääkevalmistetta

Ei

Tutkii yhdysvaltalaista FDA sääntelemää laitetuotetta

Ei

Nämä tiedot haettiin suoraan verkkosivustolta clinicaltrials.gov ilman muutoksia. Jos sinulla on pyyntöjä muuttaa, poistaa tai päivittää tutkimustietojasi, ota yhteyttä register@clinicaltrials.gov. Heti kun muutos on otettu käyttöön osoitteessa clinicaltrials.gov, se päivitetään automaattisesti myös verkkosivustollemme .

Kliiniset tutkimukset Oculomotor Exercise Program

Tilaa