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Effects of Reformer Pilates and Vestibular Exercise Programs on Balance and Gait in Children With Visual Impairment

31. srpna 2026 aktualizováno: Marmara University

Effects of Different Exercise Programs on Balance Performance and Gait Biomechanics in Children With Visual Impairment

This study looks at whether Reformer Pilates can help children and adolescents with visual impairment improve their balance, walking patterns, and muscle strength.

Participants are between 10 and 17 years old. They are randomly placed into one of two groups: an exercise group or a control group.

Those in the exercise group take part in 12 supervised Reformer Pilates sessions over 6 weeks, meeting twice a week. Those in the control group keep up with their usual daily activities and do not join the exercise program during this time.

Before and after the 6-week period, researchers measure each participant's balance, walking patterns, and muscle strength. They then compare how much each group changed.

Přehled studie

Typ studie

Intervenční

Zápis (Aktuální)

75

Fáze

  • Nelze použít

Kontakty a umístění

Tato část poskytuje kontaktní údaje pro ty, kteří studii provádějí, a informace o tom, kde se tato studie provádí.

Studijní místa

    • Istanbul
      • Istanbul, Istanbul, Turecko (Türkiye)
        • Türkan Sabancı Görme Engelliler Okulu

Kritéria účasti

Výzkumníci hledají lidi, kteří odpovídají určitému popisu, kterému se říká kritéria způsobilosti. Některé příklady těchto kritérií jsou celkový zdravotní stav osoby nebo předchozí léčba.

Kritéria způsobilosti

Věk způsobilý ke studiu

  • Dítě

Přijímá zdravé dobrovolníky

Ne

Popis

Inclusion Criteria:

  • Children and adolescents aged 10 to 17 years
  • Diagnosis of visual impairment, classified as degree 2 to 5
  • informed consent provided by a parent or legal guardian

Exclusion Criteria:

  • Presence of an orthopedic disorder affecting balance, gait, or participation in the exercise program
  • Presence of a neurological disorder affecting balance, gait, or participation in the exercise program
  • Use of medications known to affect balance or gait

Studijní plán

Tato část poskytuje podrobnosti o studijním plánu, včetně toho, jak je studie navržena a co studie měří.

Jak je studie koncipována?

Detaily designu

  • Primární účel: Léčba
  • Přidělení: Randomizované
  • Intervenční model: Paralelní přiřazení
  • Maskování: Žádné (otevřený štítek)

Zbraně a zásahy

Skupina účastníků / Arm
Intervence / Léčba
Experimentální: Pilates (Equipment-Based Pilates(Reformer)) Group
Participants in this arm received a supervised Reformer Pilates exercise program twice weekly for 6 weeks, for a total of 12 sessions
Participants in this arm attended a supervised Reformer Pilates program, held twice a week for six weeks (12 sessions in total). Sessions were structured around the Reformer apparatus and followed a progressive format, with exercise difficulty gradually increasing as participants advanced through the program.
Experimentální: Vestibular Exercise Group
Participants in this group receive a supervised vestibular balance exercise program for 6 weeks, consisting of 12 sessions (two sessions per week).
Participants in this arm attended a supervised vestibular balance exercise program, held twice a week for six weeks (12 sessions in total). Exercises were performed under varying sensory conditions and progressed in difficulty as participants advanced through the program.
Žádný zásah: Control Group
Participants in this arm continued their usual daily activities and did not receive either of the study exercise programs during the study period.

Co je měření studie?

Primární výstupní opatření

Měření výsledku
Popis opatření
Časové okno
Static Balance Performance: Center of Pressure Sway Area
Časové okno: Baseline and post-intervention at Week 6
Center of Pressure Sway Area: Static balance performance is assessed using the TekScan pressure platform. Center of pressure (COP) sway area is measured during standardized quiet standing and expressed in square centimeters (cm²) and Higher values indicate greater postural sway.
Baseline and post-intervention at Week 6
Static Balance Performance: Center of Pressure Path Length
Časové okno: Baseline and post-intervention at Week 6
Center of pressure path length is measured using the TekScan pressure platform during quiet standing, representing the total displacement distance of the center of pressure, expressed in centimeters (cm).
Baseline and post-intervention at Week 6
Static Balance Performance: Antero-posterior Center of Pressure Excursion
Časové okno: Baseline and post-intervention at Week 6
Anteroposterior center of pressure excursion is measured using the TekScan pressure platform during quiet standing, representing postural sway in the forward-backward direction, expressed in centimeters (cm).
Baseline and post-intervention at Week 6
Static Balance Performance: Mediolateral Center of Pressure Excursion
Časové okno: Baseline and post-intervention at Week 6
Medio-lateral center of pressure excursion is measured using the TekScan pressure platform during quiet standing, representing postural sway in the side-to-side direction, expressed in centimeters (cm).
Baseline and post-intervention at Week 6
Gait - Spatiotemporal:Walking Speed
Časové okno: Baseline and post-intervention at Week 6
Walking speed is assessed using the iSen Inertial Motion Capture System by STT Systems (iSEN IMUs )during the walking test and it is expressed in meters per second (m/s).
Baseline and post-intervention at Week 6
Gait - Spatiotemporal: Gait Cadence
Časové okno: Baseline and post-intervention at Week 6
Gait cadence is assessed using the iSen IMUs and it represents the average number of steps taken per minute during walking.
Baseline and post-intervention at Week 6
Gait - Spatiotemporal: Step Length and Stride Length During Gait
Časové okno: Baseline and post-intervention at Week 6
Step length and stride length are assessed using the iSEN IMU system during walking, expressed in meters (m). Step length represents the average distance between consecutive foot contacts of opposite feet and stride length represents the average distance between successive contacts of the same foot.
Baseline and post-intervention at Week 6
Pelvic Symmetry
Časové okno: Baseline and post-intervention at Week 6
Pelvic symmetry during gait is assessed using the iSEN IMUs and it is expressed as a percentage (%).
Baseline and post-intervention at Week 6
Gait: Stance and Swing Phase Duration
Časové okno: Baseline and post-intervention at Week 6
During Gait Stance and swing phase durations are assessed bilaterally using the iSEN IMUs. Stance phase represents the portion of the gait cycle during which the foot is in contact with the ground, and swing phase represents the portion during which the foot is not in contact with the ground. Values are recorded separately for the right and left limbs, expressed in seconds and as a percentage of the gait cycle.
Baseline and post-intervention at Week 6
Gait: Double Support Duration During Gait
Časové okno: Baseline and post-intervention at Week 6
Double support duration is assessed bilaterally using iSEN IMUs and represents the portion of the gait cycle during which both feet are concurrently in contact with the ground. Values are recorded separately for the right and left limbs, expressed as a percentage of the gait cycle.
Baseline and post-intervention at Week 6
Gait Kinematics: Hip Flexion-Extension Angle During Gait
Časové okno: Baseline and post-intervention at Week 6
Hip flexion and extension angles during the gait cycle are assessed bilaterally using the iSEN IMUs and expressed in degrees (º). Maximum hip flexion angle and minimum hip extension angle are recorded separately for the right and left limbs.
Baseline and post-intervention at Week 6
Gait Kinematics: Hip Flexion-Extension Range of Motion During Gait
Časové okno: Baseline and post-intervention at Week 6
Hip flexion-extension range of motion during the gait cycle is assessed bilaterally using the iSEN IMUs and expressed in degrees (º),it is recorded separately for the right and left limbs.
Baseline and post-intervention at Week 6
Gait Kinematics: Knee Flexion-Extension Angle During Gait
Časové okno: Baseline and post-intervention at Week 6
Knee flexion and extension angles during the gait cycle are assessed bilaterally using the iSEN IMUs and expressed in degrees (º). Maximum knee flexion angle and minimum knee extension angle are recorded separately for the right and left limbs.
Baseline and post-intervention at Week 6
Gait Kinematics: Knee Flexion-Extension Range of Motion During Gait
Časové okno: Baseline and post-intervention at Week 6
Knee flexion-extension range of motion during the gait cycle is assessed bilaterally using the iSEN IMUs and expressed in degrees (º), recorded separately for the right and left limbs.
Baseline and post-intervention at Week 6
Gait Kinematics: Ankle Dorsiflexion-Plantarflexion Angle During Gait
Časové okno: Baseline and post-intervention at Week 6
Ankle dorsiflexion and plantarflexion angles during the gait cycle are assessed bilaterally using the iSEN IMUs and expressed in degrees (º). Maximum dorsiflexion angle and minimum plantarflexion angle are recorded separately for the right and left limbs.
Baseline and post-intervention at Week 6
Gait Kinematics: Ankle Dorsiflexion-Plantarflexion Range of Motion During Gait
Časové okno: Baseline and post-intervention at Week 6
Ankle dorsiflexion-plantarflexion range of motion during the gait cycle is assessed bilaterally using the iSEN IMUs system and expressed in degrees (º), it is recorded separately for the right and left limbs.
Baseline and post-intervention at Week 6
Gait Kinematics: Pelvic Tilt Angle During Gait
Časové okno: Baseline and post-intervention at Week 6
Maximum posterior and anterior pelvic tilt angles during the gait cycle are assessed using the iSEN IMUs inertial measurement unit system and expressed in degrees (º), recorded separately as posterior tilt and anterior tilt values.
Baseline and post-intervention at Week 6
Gait Kinematics: Pelvic Tilt Range of Motion
Časové okno: Baseline and post-intervention at Week 6
Pelvic tilt range of motion during the gait cycle is assessed using the iSEN IMUs , representing the combined anterior (posterior tilt) and interior (anterior tilt) excursion, expressed in degrees (º).
Baseline and post-intervention at Week 6

Sekundární výstupní opatření

Měření výsledku
Popis opatření
Časové okno
Muscle Strength: Isometric Knee Extensor Muscle Strength
Časové okno: Baseline and post-intervention at Week 6
Knee Extension Isometric Strength Assessment: Participants will sit with knees at ~90° flexion, feet unsupported, distal posterior thigh positioned ~10 cm from the chair's front edge, arms on the armrests with hands gripping the handles, and thighs/pelvis stabilized with a strap. A dynamometer will be fixed to an apparatus mounted behind the chair using a rigid, non-stretch strap positioned ~2 cm proximal to the lateral malleolus and secured across the anterior tibial surface; participants will perform knee extension, applying maximal isometric force against the dynamometer through the strap. Three 5-second maximal contractions will be performed, with 1-minute rest between trials and verbal encouragement to ensure maximal effort; peak force will be recorded for each trial.
Baseline and post-intervention at Week 6
Muscle Strength: Isometric Knee Flexor Muscle Strength
Časové okno: Baseline and post-intervention at Week 6
Knee Flexion Isometric Strength Assessment: Participants will sit with feet unsupported, arms on the armrests with hands gripping the handles, and popliteal fossa positioned ~10 cm anterior to the chair's front edge, with thighs/pelvis stabilized using a strap. A dynamometer will be fixed to an apparatus mounted in front of the chair using a rigid, non-stretch strap positioned ~2 cm proximal to the lateral malleolus and secured across the posterior tibial surface; participants will flex the knee to 90° and apply maximal isometric force against the dynamometer through the strap. Three 5-second maximal contractions will be performed, with 1-minute rest between trials and verbal encouragement to ensure maximal effort; peak force will be recorded for each trial.
Baseline and post-intervention at Week 6
Trunk Muscle Endurance: Trunk Flexor Endurance
Časové okno: Baseline and post-intervention at Week 6
Trunk flexor endurance is assessed using a 1-minute curl-up test. Participants perform repeated curl-ups from a supine position with knees flexed at 90°, sliding their hands forward toward the knees and returning to the starting position with proper form. The number of correctly completed repetitions within 1 minute is recorded.
Baseline and post-intervention at Week 6
Trunk Extensor Endurance
Časové okno: Baseline and post-intervention at Week 6
Description: Trunk extensor endurance is assessed using a modified Sørensen test performed on a Roman chair, with the pelvis and lower extremities secured. Participants cross their arms over the chest and maintain the trunk horizontally aligned with the lower extremities, knees extended, for as long as possible. The test is terminated when the participant can no longer sustain the position, and the duration is recorded in seconds.
Baseline and post-intervention at Week 6

Spolupracovníci a vyšetřovatelé

Zde najdete lidi a organizace zapojené do této studie.

Vyšetřovatelé

  • Vrchní vyšetřovatel: Selda Uzun, PhD, Marmara University

Termíny studijních záznamů

Tato data sledují průběh záznamů studie a předkládání souhrnných výsledků na ClinicalTrials.gov. Záznamy ze studií a hlášené výsledky jsou před zveřejněním na veřejné webové stránce přezkoumány Národní lékařskou knihovnou (NLM), aby se ujistily, že splňují specifické standardy kontroly kvality.

Hlavní termíny studia

Začátek studia (Aktuální)

14. února 2025

Primární dokončení (Odhadovaný)

30. listopadu 2026

Dokončení studie (Odhadovaný)

25. prosince 2026

Termíny zápisu do studia

První předloženo

24. srpna 2026

První předloženo, které splnilo kritéria kontroly kvality

24. srpna 2026

První zveřejněno (Aktuální)

27. srpna 2026

Aktualizace studijních záznamů

Poslední zveřejněná aktualizace (Aktuální)

2. září 2026

Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality

31. srpna 2026

Naposledy ověřeno

1. srpna 2026

Více informací

Termíny související s touto studií

Plán pro data jednotlivých účastníků (IPD)

Plánujete sdílet data jednotlivých účastníků (IPD)?

NE

Popis plánu IPD

Individual participant data will not be made available to other researchers. Because the study population consists of children, data sharing is restricted in line with the permission obtained from the Provincial Directorate of National Education. Study results will only be presented in aggregate form, without any information that could identify individual participants.

Informace o lécích a zařízeních, studijní dokumenty

Studuje lékový produkt regulovaný americkým FDA

Ne

Studuje produkt zařízení regulovaný americkým úřadem FDA

Ne

Tyto informace byly beze změn načteny přímo z webu clinicaltrials.gov. Máte-li jakékoli požadavky na změnu, odstranění nebo aktualizaci podrobností studie, kontaktujte prosím register@clinicaltrials.gov. Jakmile bude změna implementována na clinicaltrials.gov, bude automaticky aktualizována i na našem webu .

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