- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01845948
Effectiveness of a Parental Training Programme to Enhance Parent-child Relationship and Reduce Harsh Parenting Practices and Parental Stress in the Preparation of Children for Transition to Primary School
Effectiveness of a Parental Training Programme to Enhance Parent-child Relationship and Reduce Harsh Parenting Practices and Parental Stress in the Preparation of Children for Transition to Primary School: A Randomized Controlled Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Introduction Transition creates a time of vulnerability for the child, the parents and their relationship. Failure to adjust to the transition, on the part of either parents or children, might place the family in a psychological devastating position. There is an imperative need to develop and evaluate appropriate interventions for parents so that they can contribute to helping their children enjoy a smooth passage to a pleasurable learning life in primary school.
Aim The aims of this study were to test the effectiveness of a parental training programme to enhance parent-child relationship and reduce harsh parenting practices and parental stress in the preparation of children for transition to primary school.
Methods A randomized controlled trial, two-group pre-test and repeated post-test, between-subjects design was employed. The method of simple complete randomization was adopted. Recruitment and data collection were conducted during the summer in 2009. Participants were recruited through referrals from the Hong Kong Sheung Kung Hui Welfare Council in Tung Chung. Written consent was obtained from parents after they were told the purposes of the study and agreed to participate. Parents were told that they were under no obligation to participate, could withdraw from the study with impunity at any time and were assured of the confidentiality of the data to be collected.
After they had signed consent forms, a research assistant collected demographic and baseline data from parents. Data collection was divided into three phases: at the time of recruitment (pre-intervention), at six weeks and three months after the intervention. Parents were asked to respond to the Chinese version of the parental acceptance-rejection scale, parental stress scale, and self-report scale on parent-child relationship in respect of the transition from kindergarten to primary school.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Hong Kong, China
- Hong Kong Sheng Kung Hui Tung Chung Integrated Services
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- must be able to read and write Chinese
- must have had primary school education or above
Exclusion Criteria:
- with identified cognitive and learning problems were excluded, as also were children with such problems
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Placebo Comparator: Placebo Control
Parents had no intervention except that an information leaflet for parents on helping children to adapt the new primary school life published by Education Bureau was given to each parent in the control group at the end of data collection.
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Parents had no intervention except that an information leaflet for parents on helping children to adapt the new primary school life published by Education Bureau was given to each parent in the control group at the end of data collection.
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Experimental: parental training programme
The parental training programme was run in small groups of 8 to 12 parents over four consecutive weeks.
They consisted of four group sessions, each lasting about two hours.
The major focus of the parental intervention included teaching parents: (1) to use more active listening skills, (2) to engage less in harsh parenting practices, (3) to use more praise and encouragement and (4) to set reasonable expectations in the rearing of their children.
Each session was started with revision of skills or concepts discussed in previous sessions, therefore, each session built on the previous session.
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In the experimental group, parents participated in the parental training programme approximately one month before the start of the academic year in primary school.
Two social workers, who have minimum five- year experience in giving family counselling,implemented the interventions.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change of Self-reported Parent-Child Relationship at 6 weeks from baseline
Time Frame: 6 weeks
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The parent-child relationship of the participants was measured by using a self-reporting method consisting of two items, with one asking 'How satisfied are you with the parent-child relationship?"
and the other 'As a parent, how satisfied are you with yourself?'
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6 weeks
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Self-reported Parent-Child Relationship at baseline
Time Frame: baseline, 0 week ( just before the start of intervention)
|
The parent-child relationship of the participants was measured by using a self-reporting method consisting of two items, with one asking 'How satisfied are you with the parent-child relationship?"
and the other 'As a parent, how satisfied are you with yourself?'
|
baseline, 0 week ( just before the start of intervention)
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Change of Self-reported Parent-Child Relationship at 3 months from baseline
Time Frame: 3 months
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The parent-child relationship of the participants was measured by using a self-reporting method consisting of two items, with one asking 'How satisfied are you with the parent-child relationship?"
and the other 'As a parent, how satisfied are you with yourself?'
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3 months
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Perceived Parental Aggression Scale at baseline
Time Frame: baseline, 0 week ( just before the start of intervention)
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It measures harsh parenting, i.e. physical or verbal aggression towards children
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baseline, 0 week ( just before the start of intervention)
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change of Perceived Parental Aggression Scale at 6 weeks from baseline
Time Frame: 6 weeks
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It measures harsh parenting, i.e. physical or verbal aggression towards children
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6 weeks
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change of Perceived Parental Aggression Scale at 3 months from baseline
Time Frame: 3 months
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It measures harsh parenting, i.e. physical or verbal aggression towards children
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3 months
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Parental Stress at baseline
Time Frame: baseline, 0 week ( just before the start of intervention)
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we assess a parent's subjective feelings of strain, difficulty and dissatisfaction in reaction to stressors in the parent-child relationship
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baseline, 0 week ( just before the start of intervention)
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change of Parental Stress at baseline at 6 weeks from baseline
Time Frame: 6 weeks
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we assess a parent's subjective feelings of strain, difficulty and dissatisfaction in reaction to stressors in the parent-child relationship
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6 weeks
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change of Parental Stress at baseline at 3 months from baseline
Time Frame: 3 months
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we assess a parent's subjective feelings of strain, difficulty and dissatisfaction in reaction to stressors in the parent-child relationship
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3 months
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: William Ho Cheung Li, PhD, The School of Nursing, The University of Hong Kong
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- ND789
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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