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- Klinische proef NCT07635706
Effects of a Vision-Focused Occupational Therapy Program on Visual Skills in Primary School Children
The Effect of a Vision-Focused Occupational Therapy Program on Visual Perception and School-Based Visual-Motor Functions in Primary School Children
Studie Overzicht
Toestand
Conditie
Interventie / Behandeling
Gedetailleerde beschrijving
Visual skills, including visual perception, visual-motor integration, visual scanning, eye movement control, and convergence ability, are important determinants of academic performance and school participation. Previous research has demonstrated associations between visual skills and reading, writing, attention, and motor performance; however, experimental studies evaluating structured occupational therapy interventions targeting visual skills in typically developing school-aged children remain limited.
The purpose of this randomized controlled trial is to examine the effectiveness of a structured visual skills-based occupational therapy program on visual perception and school-based visual-motor functions in typically developing primary school students.
Participants aged 8-10 years attending the 3rd and 4th grades of primary school will be recruited and randomly assigned to intervention and control groups. The intervention group will receive a 6-week occupational therapy program consisting of visual skills activities focusing on oculomotor functions, visual perception, visual scanning, eye-hand coordination, and visual-motor integration. Sessions will be conducted twice weekly in the school setting.
Outcome measures include the Motor-Free Visual Perception Test-3 (MVPT-3), Minnesota Handwriting Assessment (MHA), Near Point of Convergence (NPC), and Bruininks-Oseretsky Test of Motor Proficiency-2 Short Form (BOT-2 SF). Assessments will be performed before and after the intervention period.
Findings from this study are expected to contribute to the evidence base for school-based occupational therapy interventions targeting visual skills in typically developing children.
Studietype
Inschrijving (Geschat)
Fase
- Niet toepasbaar
Contacten en locaties
Studie Locaties
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Istanbul
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Istanbul, Istanbul, Turkije (Türkiye)
- Werving
- Güngören Yahya Çavuş İlkokulu
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Contact:
- Merve Keskin, MSc
- Telefoonnummer: +90 5375825256
- E-mail: mervekeskiin98@gmail.com
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Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Kind
Accepteert gezonde vrijwilligers
Beschrijving
Inclusion Criteria:
- Children aged 8 to 10 years
- Enrollment in 3rd or 4th grade of primary school
- Ability to understand and follow study instructions
- Written informed consent obtained from parent or legal guardian
- Willingness to participate in all assessment and intervention sessions
Exclusion Criteria:
- Diagnosed neurological, psychiatric, developmental, or intellectual disorder
- Uncorrected visual impairment that may affect assessment results
- Musculoskeletal condition affecting upper extremity function
- Participation in another structured visual training or rehabilitation program during the study period
- Inability to complete study assessments or intervention sessions
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Enkel
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
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Experimenteel: Visual Skills-Based Occupational Therapy Program
Participants receive a structured visual skills-based occupational therapy program twice weekly for 6 weeks in the school setting.
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A structured occupational therapy program delivered twice weekly for 6 weeks targeting oculomotor functions, visual perception, visual scanning, eye-hand coordination, convergence, and visual-motor integration.
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Actieve vergelijker: Home Program Control
Participants continue routine school activities and receive structured home-based assignments without visual skills training.
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Participants continue routine school activities and receive structured home-based assignments without visual skills training during the study period.
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Motor-Free Visual Perception Test-3 (MVPT-3) Score
Tijdsspanne: Baseline and 6 weeks
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Visual perception will be assessed using the Motor-Free Visual Perception Test-3 (MVPT-3).
Higher scores indicate better visual perception performance.
Visual perception will be assessed using the Motor-Free Visual Perception Test, Fourth Edition (MVPT-4).
Total scores range from 0 to 45, with higher scores indicating better visual perceptual ability.
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Baseline and 6 weeks
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Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Minnesota Handwriting Assessment (MHA) Score
Tijdsspanne: Baseline and 6 weeks
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Handwriting performance will be evaluated using the Minnesota Handwriting Assessment, including legibility and writing quality parameters.
Handwriting performance will be evaluated using the Minnesota Handwriting Assessment (MHA).
The assessment evaluates legibility and handwriting quality.
Scores range from 0 to 34 for each handwriting component, with higher scores indicating better handwriting performance.
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Baseline and 6 weeks
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Bruininks-Oseretsky Test of Motor Proficiency-2 Short Form (BOT-2 SF) Score
Tijdsspanne: Baseline and 6 weeks
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Motor proficiency will be assessed using the BOT-2 Short Form.
Higher scores indicate better motor performance.
Motor proficiency will be assessed using the Bruininks-Oseretsky Test of Motor Proficiency, Second Edition, Short Form (BOT-2 SF).
Total point scores range from 0 to 88, with higher scores indicating better motor proficiency.
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Baseline and 6 weeks
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Medewerkers en onderzoekers
Sponsor
Studie record data
Bestudeer belangrijke data
Studie start (Werkelijk)
Primaire voltooiing (Geschat)
Studie voltooiing (Geschat)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Andere studie-ID-nummers
- VOT-TR-2026
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
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