Improving emotional regulation skills in children from difficult backgrounds in Shenzhen
Improving Emotional Regulation Skills of Children in Difficulty in Shenzhen
This study is testing a program to help children aged 8 to 14 from tough backgrounds in Shenzhen learn better ways to manage their emotions.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 200 (estimated) |
| Ages | 8 Years to 14 Years |
| Sex | All |
| Sponsor | City University of Hong Kong Academic / other |
| Locations | 1 site (Hong Kong) |
| Trial ID | NCT06331936 on ClinicalTrials.gov |
What this trial studies
This study aims to enhance emotional regulation strategies among children aged 8 to 14 who come from challenging backgrounds in Shenzhen, including single-parent, low-income, and left-behind families. Utilizing a randomized wait-list control trial design, 200 participants will be assigned to either an experimental group receiving intervention or a wait-list control group. The intervention consists of four sessions, each lasting 1.5 to 2 hours, followed by a booster session. Assessments will be conducted at three time points to evaluate the effectiveness of the intervention.
Who should consider this trial
Good fit: Ideal candidates for this study are children aged 8 to 14 from single-parent families, low-income families, or those identified as left-behind children.
Not a fit: Children with a history of severe psychotic symptoms or those who have previously participated in a similar intervention program may not benefit from this study.
Why it matters
Potential benefit: If successful, this intervention could significantly improve emotional regulation and overall well-being in children facing adversity.
How similar studies have performed: Other studies have shown success in improving emotional regulation in children using similar intervention approaches, although this specific adaptation for mainland China is novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * single-parent families * low-income families * left-behind children Exclusion Criteria: * a history of severe psychotic symptoms * have previously participated in a similar intervention program
Where this trial is running
Hong Kong
- City University of Hong Kong — Hong Kong, China (Recruiting)
Study contacts
- Principal investigator: Nancy YU, Dr. — City University of Hong Kong
- Study coordinator: Nancy YU, Dr.
- Email: nancy.yu@cityu.edu.hk
- Phone: 34429436
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.