Skip to main content
OpenTrials
Completed

NCT Number: NCT04524923

Touch Screen Usage Time In Relation To Visual Motor Integration and Quality of Life In Preschoolers

Recent literatures are associating digital technology extensive and addictive use with physical, psychosocial and cognitive inverse consequences. This research focuses more on number of touch screen devices; age started using devices and usage time in relation to cognitive function in preschoolers.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Age range

3 year–5 year

Sex eligibility

All sexes

Study type

Observational

Primary location

faculty of physical therapy, Cairo university

Giza, 12662, Egypt

About this study

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.

Who can participate

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Visual Motor Integration

Other

investigate the relation between touch screen usage and visual motor integration in preschoolers

Quality of Life Assessment

Other

investigate the relation between touch screen usage and Quality of life assessment in preschoolers

Cognitive Functioning

Other

investigate the relation between touch screen usage and Cognitive Functioning assessment in preschoolers

Primary outcomes

  1. visual motor integration

    Time frame: 1 September 2020 to 31 March 2021

    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

  2. Physical and Psychosocial Health

    Time frame: 1 September 2020 to 31 March 2021

    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.

  3. cognitive function

    Time frame: 1 September 2020 to 31 March 2021

    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.

Sponsors and collaborators

Lead sponsor

Cairo University

Other

Registry information

Official study title

Touch Screen Usage Time In Relation To Visual Motor Integration and Quality of Life In Preschoolers: A Cross Sectional Study

Important dates

Study start
2020
Primary completion
2021
Study completion
2021
First posted
Aug 24, 2020
Registry last updated
Jun 30, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.