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A multi-component intervention to Reduce Screen-Based Sedentary Behavioursâ?? in 2-5 years children in Chandigarh

A Randomized Control Trial to Reduce Screen-Based Sedentary Behaviorsâ?? in 2-5 years Children in Chandigarh

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/09/009761
Enrollment
428
Registered
2017-09-14
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: Disseminating information among parents regarding normal developmental stages of children and effects of screen-time.: Child strategies will be alternatives to digital screen watching.

Sponsors

Indian Council of Medical Research
Lead Sponsor
Madhu Gupta
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1. Parents of children [age 2- 5 (± 3 months) years] who are willing to be a part of the study and give written consent. 2. Families who have been residing in Chandigarh since past one year and intend to stay in Chandigarh till the intervention and follow up is completed.

Exclusion criteria

Exclusion criteria: 1. Participants whose parents are not willing to give consent 2. Children who have been previously diagnosed with any chronic disease and are on long- term treatment. 3. Families who have not been residing in Chandigarh since past one year 4. Families who do not intend to stay in Chandigarh till the intervention and follow up are completed.

Design outcomes

Primary

MeasureTime frame
Digital screen time will be measured using a pretested, semi-structured questionnaire. It will be bilingual i.e. Hindi/ English. This questionnaire will provide information on the background information of the family, average screen time of the child, parent perceptions etc. The interviewer will fill this questionnaire with the help of parents of the child.Timepoint: Baseline survey at the start of the trial, End-line survey at the end of the trial, First follow-up at three months then Second follow-up at 6 months after the trial.

Secondary

MeasureTime frame
For childs deranged sleep behaviours- Sleep disturbance scale for children (SDSC) will be used. This will be filled by the interviewer and reported by parents.Timepoint: Baseline survey at the start of the trial, End-line survey at the end of the trial, First follow-up at three months then Second follow-up at 6 months after the trial.;For Childs emotional and behavioural development Pre-school behaviour check list (PBCL) will be used. It will be completed by the interviewer and reported by parents.Timepoint: Baseline survey at the start of the trial, End-line survey at the end of the trial, First follow-up at three months then Second follow-up at 6 months after the trial.;Physical activity will be measured using a pretested, semi- structured questionnaire. This questionnaire will be filled by the interviewer and reported by the parents of the child.Timepoint: Baseline survey at the start of the trial, End-line survey at the end of the trial, First follow-up at three months then Second follow-up at 6 months after the trial.

Countries

India

Contacts

Public ContactNimran Kaur

Post Graduate Institute of Medical Education and Research

madhugupta21@gmail.com7009769629

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 16, 2026