Be Good Parents (Parent Education)

NCT02986009 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 353

Last updated 2018-01-25

No results posted yet for this study

Summary

The collaborator has its vision as "To have children, individuals, families and migrants across countries live in dignity and harmony, and be contributing members to a just, humane and caring society." Parents are very significant in the families as they need nurturing, discipline, teaching, monitoring, and managing their children as well as their families. Capable and competent parents bring good child outcome and happy family. The investigators planned to serve targeted parents in two areas as 1. Emotion management and 2. Information on community resource. In the first set, the participants are expected to improve their emotion management leading to a more effective parenting. In the second set, the participants would acquire more information that enables them to better use the community resources.

To work closely with the collaborator, and based on the previous results of an effective parenting intervention, the investigators will modify the intervention to tailor the needs of targeted parents. The objectives are:

1. After completing the parenting intervention, 150 participants will, 1.1. To increase participants' emotion management strategies by 20%, 1.2. To enhance positive affect by 10%, 1.3. To decrease negative affect by 10%, 1.4. To enhance satisfaction with the parent-child relationship by 10%, 1.5. To increase subjective happiness by 8%, 1.6. To enhance family harmony by 5%, These levels of positive effects of the program were projected from the investigators' published findings.
2. After joining the information sessions about education, health care, housing, employment, and community facilities, another 150 participants will, 2.1 To know more information of Hong Kong by 50%, 2.2 To know more information of Mainland China by 50%, 2.3 To use more community resources either in Hong Kong or Mainland China by 50%.

To study the effectiveness of parenting intervention, the investigators proposed to use a randomized controlled trial (RCT) that is a type of scientific study to reduce bias. Participants in this project will be randomly allocated to either the emotional management group or the information group. As the information group has no focus on parenting, participants would show no significant improvement in emotion management strategies or satisfaction with the parent-child relationship, etc. Meanwhile, participants in the parenting intervention would show no significant improvement in knowledge about either Hong Kong or Mainland China.

Conditions

  • Parenting

Interventions

BEHAVIORAL

Parenting

The parenting intervention consists of four weekly sessions, each lasting two hours. The intervention was designed according to the parenting characteristics of Chinese parents in Hong Kong. The four sessions cover: 1) response modification ("stop and rest"), 2) relaxation/enhancing positive moods ("relax and play"), 3) cognitive reframing ("think"), and 4) using social support ("talk and share). Discussion, practice, and questions are involved in each session.

BEHAVIORAL

Information

The information intervention consists of four weekly sessions, each lasting for two hours. The contents cover information and resources about education, medical care, housing, employment, and community facilities available in Hong Kong and Mainland China.

Sponsors & Collaborators

  • International Social Service Hong Kong Branch

    collaborator UNKNOWN
  • City University of Hong Kong

    lead OTHER

Principal Investigators

  • Nancy Xiaonan Yu · City University of Hong Kong

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-03-02
Primary Completion
2017-11-29
Completion
2018-01-15

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02986009 on ClinicalTrials.gov