Examining the feasibility of carrying out a parent-administered screen time intervention in toddlers

Not Applicable

Completed

• Conditions: The impact of toddler screen time in the hour before bed on their sleep and attention; Not Applicable

• Registration Number: ISRCTN58249751
• Lead Sponsor: Birkbeck, University of London

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2022-04-29
• Study Completion: 2023-07-30
• Last Update Posted: 15 July 2024

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 105

Inclusion Criteria

Current inclusion criteria as of 22/07/2022:

Inclusion criteria will be assessed using a Family Background Pre-screen Questionnaire. Potential participants will be invited to take part in PASTI if they meet the following inclusion criteria:
1. A family with an infant between 16 and 30 months at pre-screening
2. A family that lives in Central/Greater London and surrounding areas (within 75 miles of the Birkbeck Babylab)
3. A family that reports that their infant uses screen time in the hour before bed at pre-screening. They must report that their infant uses =10 minutes of screen time in the hour before bed on =3 days of the week.
4. A caregiver is able to provide informed consent

____

Previous inclusion criteria:

Inclusion criteria will be assessed using a Family Background Pre-screen Questionnaire. Potential participants will be invited to take part in PASTI if they meet the following inclusion criteria:
1. A family with an infant between 16 and 18 months at pre-screening
2. A family that lives in Central/Greater London
3. A family that reports that their infant uses screen time in the hour before bed at pre-screening. They must report that their infant uses =10 minutes of screen time in the hour before bed on =3 days of the week.
4. A caregiver is able to provide informed consent

Exclusion Criteria

Exclusion criteria will be assessed using a Family Background Pre-screen Questionnaire. Potential participants will be excluded if they meet the following criteria:
1. A family with an infant who has a parent-reported genetic or neurological condition (e.g., Downs Syndrome)
2. A family with an infant who was born prematurely (<37 weeks)
3. A family with an infant who is taking part in another trial or research study

Study & Design

• Study Type: Interventional
• Study Design: Not specified