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Clinical Trials/NCT00959309
NCT00959309CompletedPhase 4

Media Use in Preschooler Study (MUPS) An Office Based Intervention to Improve Media Use in Preschool Children: a Randomized Controlled Trial

The Hospital for Sick Children1 site in 1 country160 target enrollmentStarted: October 1, 2007Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Phase 4
Status
Completed
Enrollment
160
Locations
1
Primary Endpoint
Parent reported number of hours screen time on the previous weekday and previous weekend day

Study Overview

Brief Summary

Childhood obesity is an epidemic and increasing. There are very few effective treatments for obesity in children. Recent studies have shown an association between obesity and sedentary behaviors such as television, video viewing and playing video games ('screen time') in preschool aged children. A school based intervention to reduce screen time in older children has been effective in preventing obesity.

The reduction of screen time may lead to the prevention of obesity and its complications in preschool children.

Detailed Description

There have been no trials examining an intervention to decrease screen time in preschool children in the physician office setting. This setting is appealing for interventions directed to preschool children because of accessibility. In addition, other public health interventions implemented in a physician office setting, such as home safety advice, have been effective.

The proposed study design will be a randomized controlled trial. The intervention group will receive the study intervention, which is a 15 minute session about the health impact of screen time in children and strategies to decrease screen time.

The objective of this study is to determine if an office based intervention is effective in decreasing screen time (television, video viewing and playing video games) in preschool children.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Triple (Participant, Care Provider, Investigator)

Eligibility Criteria

Ages
3 Years to 3 Years (Child)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •registered to attend a 3 year old well child visit

Exclusion Criteria

  • •children with limitations in ambulation or cognitive delay will be excluded from the study.

Arms & Interventions

Intervention

Experimental

Intervention: Strategies to decrease screen time in children (Behavioral)

Control

Active Comparator

Intervention: Non-Strategical Media Education (Behavioral)

Outcomes

Primary Outcomes

Parent reported number of hours screen time on the previous weekday and previous weekend day

Time Frame: 6 and 12 months

Secondary Outcomes

  • Number of meals in front of the TV(6 and 12 months)
  • Activity levels(6 and 12 months)
  • Anthropometric measures(12 months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Catherine Birken

Staff Paediatrician

The Hospital for Sick Children

Study Sites (1)

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