Ignite Creation Date:
2024-10-26 @ 3:41 PM
Last Modification Date:
2024-10-26 @ 3:41 PM
Study NCT ID:
NCT06620250
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-09-25
Brief Title:
A Study of the Impact of Digital Intervention on Parentsprimary Caregivers Myopia Prevention and Control Health Literacy on Preschoolers Myopia and Physical and Mental Health
Sponsor:
None
Organization:
None
Study Overview
Official Title:
A Randomized Controlled Triala Study of the Impact of Digital Intervention on Parentsprimary Caregivers Myopia Prevention and Control Health Literacy on Preschoolers Myopia and Physical and Mental Health
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The study is a Randomized controlled trial based on digital interventions involving pre-school children and their parents or major caregivers To compare the myopia and physical and mental health status of preschool children before and after intervention between intervention group and control group to confirm the effect of digital intervention on prevention and control of Myopia and physical and mental health of preschool children
Detailed Description:
In this study wechat online courses live broadcast and SMS were used to transfer the knowledge of myopia prevention and control to parentsprimary caregivers and to promote their attitude and behavior change The intervention period was from October to December 2025 The control group did not 2024 any intervention The prevention and control of Myopia and health literacy of the parents and main adopters were collected at baseline and after the intervention respectively visual data and physical and mental health status of preschool children were collected every six months
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None