- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04524923
Touch Screen Usage Time In Relation To Visual Motor Integration and Quality of Life In Preschoolers
Touch Screen Usage Time In Relation To Visual Motor Integration and Quality of Life In Preschoolers: A Cross Sectional Study
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
A hundred typically developing preschool children of both genders with age ranges from three to five years will be included in this study. Visual motor integration, quality of life and cognitive function were assessed by the Peabody Developmental Motor Scale, the Pediatric Quality of Life Inventory™ and the Pediatric Quality of Life Inventory™ cognitive functioning scale respectively
Sample size To avoid type II error, sample size calculation was based on data from a pilot study on correlation between touch screen usage time and visual motor integration. Using G*POWER statistica software (version 3.1.9.2; Franz Faul, Universitat Kiel, Germany) [Correlational study, α=0.05, β=0.2, and medium effect size = 0.3] revealed that the appropriate sample size for this study was N=84 Therefore, one-hundred children were recruited for possible dropouts during assessment.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Giza, Egypt, 12662
- Faculty of Physical Therapy, Cairo University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion criteria:
Children were enrolled in this study according to the following criteria:
- Age ranges from three to five years.
- Both genders were included.
Exclusion criteria:
Children were excluded from the study if they had any of the following criteria:
- Diagnosed with attention deficit/hyperactivity disorder (ADD/ADHD) or developmental co-ordination disorder (DCD).
- Preterm children; children with major physical disabilities, genetic disorders; prenatal exposure to alcohol; children with a history of head trauma and infections.
- Diagnosed with psychiatric conditions such as autism and depression.
- Diagnosed with significant behavioral disorders
- Diagnosed with fine motor problems.
- Significant auditory or visual deficits.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
cohort group
Ninety-seven typically developing preschool children of both genders with age ranges from three to five years will be included in this study.
Visual motor integration, quality of life and cognitive function were assessed by the Peabody Developmental Motor Scale, the Pediatric Quality of Life Inventory™ and the Pediatric Quality of Life Inventory™ cognitive functioning scale respectively
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investigate the relation between touch screen usage and visual motor integration in preschoolers
investigate the relation between touch screen usage and Quality of life assessment in preschoolers
investigate the relation between touch screen usage and Cognitive Functioning assessment in preschoolers
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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visual motor integration
Time Frame: 1 September 2020 to 31 March 2021
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The Peabody Developmental Motor Scale will be used to assess visual motor integration.
It is a standardized, norm-referenced test used for the assessment of upper limb functions.
It is an early childhood motor development program that provides (in one package) both in depth assessment and training of gross and fine motor skills.
It can be used by occupational therapists, physical therapists, psychologists, and others who are interested in examining the motor abilities of young children.
It is composed of six subtests:-Reflexes (8 items), stationary (30 items), locomotion (89 items), object manipulation (24 items), grasping (25 items) and visual motor integration (72 items).
The results of the subtests may be used to generate 3 global indexes of motor performance called (composites).
These composites are gross motor quotient, fine motor quotient and total motor quotient with higher scores represent better performance
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1 September 2020 to 31 March 2021
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Physical and Psychosocial Health
Time Frame: 1 September 2020 to 31 March 2021
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The Pediatric quality of life inventory™ generic Arabic parent proxy-report for children from two to five years was used to assess quality of life.
It was developed to quantify health- related quality of life (HRQoL) of children and adolescents aged 2-18 years.
It consists of 23 questions and evaluate how frequently of a trouble the child has had over the past month.
Interpretation of the scale reveals the mean performance as total scale score, physical functioning score (eight questions), emotional functioning score (five questions), social functioning score (five questions) and school function scores (five items).
the scores are from 0 to 100 with higher results reflecting better performance.
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1 September 2020 to 31 March 2021
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cognitive function
Time Frame: 1 September 2020 to 31 March 2021
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Pediatric Quality of Life Inventory™ Cognitive Functioning Scale will be used to assess cognitive function.
It was developed as a brief generic symptom-specific instrument to measure cognitive functioning.
The 6-item scale was designed as a brief and easy-to-administer patient self-reported and parent proxy-reported generic symptom specific instrument to measure cognitive functioning across pediatric populations, originally developed in a pediatric cancer population.
The PedsQLTM Cognitive Functioning Scale includes format, instructions, Likert scale from 0 to 100 with higher scores indicating better cognitive function.
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1 September 2020 to 31 March 2021
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Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Amira M El-tohamy, Phd, Cairo University
- Study Director: Amira M Mahmoud, Cairo University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- child development
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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