Sensory Integration for Infants With Cortical Visual Impairment
NCT ID: NCT05431647
Last Updated: 2022-06-27
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
34 participants
INTERVENTIONAL
2021-01-06
2021-06-05
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
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İntervention group: Physiotherapy and Sensory Integration Therapy
Physiotherapy program
8 weeks 2 days in a week 45 minutes per session Conventional physiotherapy
Sensory integration therapy program
8 weeks 2 days in a week 45 minutes per session Sensory integration therapy
Sensory integration therapy
The individuals were divided into two as randomized controlled. Both physiotherapy and sensory integration therapy were applied to the intervention group. Each treatment was applied as 2 sessions per week, 2 days a week for 8 weeks. In the control group, only physiotherapy treatment was applied for 8 weeks, 2 days a week, 2 sessions per week.
Control group only Physiotherapy
Physiotherapy program
8 weeks 2 days in a week 45 minutes per session Conventional physiotherapy
Sensory integration therapy
The individuals were divided into two as randomized controlled. Both physiotherapy and sensory integration therapy were applied to the intervention group. Each treatment was applied as 2 sessions per week, 2 days a week for 8 weeks. In the control group, only physiotherapy treatment was applied for 8 weeks, 2 days a week, 2 sessions per week.
Interventions
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Sensory integration therapy
The individuals were divided into two as randomized controlled. Both physiotherapy and sensory integration therapy were applied to the intervention group. Each treatment was applied as 2 sessions per week, 2 days a week for 8 weeks. In the control group, only physiotherapy treatment was applied for 8 weeks, 2 days a week, 2 sessions per week.
Eligibility Criteria
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Inclusion Criteria
* Cortical visual impairment
* 12-18 months
Exclusion Criteria
12 Months
18 Months
ALL
Yes
Sponsors
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Hacettepe University
OTHER
Responsible Party
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Mustafa Cemali
Phd. student
Principal Investigators
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mustafa cemali, Phd. student
Role: STUDY_DIRECTOR
hacettepe üniversitesi
Locations
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Occupational Therapy Department
Ankara, Çankaya, Turkey (Türkiye)
Countries
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Other Identifiers
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2020-20/494
Identifier Type: -
Identifier Source: org_study_id
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