Parent-child Relationship Among Low-income Families in Hong Kong

Sponsor
The University of Hong Kong (Other)
Overall Status
Completed
CT.gov ID
NCT03185273
Collaborator
(none)
217
1
46.8
4.6

Study Details

Study Description

Brief Summary

This is a prospective cohort study building upon the existing cohort study on the effectiveness of the Trekkers Family Enhancement Scheme. This study will sample 200 low-income parent-child pairs and follow them up for 24 months with yearly assessment on parental stress and child health using both subjective measures and objective physiological parameters. Additional data on parenting style, neighbourhood cohesion, child physical assault and neglect potential, parental mental health and HRQOL and family disharmony will also be collected at each assessment time point for testing mediating and moderating mechanisms between parental stress and child health. The baseline assessment will be carried out in 2016-17 with three repeated assessments after 6 months, 12 months, and 24 months.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Study aims

    • To examine the relationship between parental stress and child health.

    • To evaluate the stress of parents as indicated by their subjective perception of mental health, quality of life and allostatic load on the body.

    • To evaluate the health of children as indicated by their well-being, behaviors, body mass index (BMI) z-score and telomere length.

    • To examine the correlation between changes in parental stress and changes in child health over time.

    • To identify the moderators and mediators of the relationship between parental stress and child health.

    Eligible participants in the main cohort study will be approached by call or during face-to-face sessions. Parents who express interest in participation will be provided with an information sheet about the research and asked to sign the consent form for themselves and for their children. After providing consent, the parent of each parent-child pair will complete a set of structured questionnaires on parental mental health and HRQOL, parenting style, neighborhood cohesion, and their children's well-being and behaviors. Physical examination including blood pressure, heart rate, weight, height, and waist-to-hip ratio will also be carried out on both parents and children. A swab of buccal cells will be taken from each child. Venous blood will be sampled from each parent.

    This study will have four assessment waves: Baseline, T2 follow up (6 months), T3 follow up (12 months), and T4 follow up (24 months). Physical health data and biological samples will be collected by research nurses and research assistants during health assessment session held in community centers. Questionnaire data will be collected by trained interviewers during telephone survey. To minimize attrition, a package of questionnaires and a sheet of instructions and equipment (i.e. brushes) for swab-taking at home may also be sent to parents upon request.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    217 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    In-depth Exploration of a Bidirectional Parent-child Relationship and Its Mediating and Moderating Factors Among Low-income Families in Hong Kong
    Actual Study Start Date :
    Mar 9, 2016
    Actual Primary Completion Date :
    Jan 9, 2020
    Actual Study Completion Date :
    Jan 31, 2020

    Outcome Measures

    Primary Outcome Measures

    1. Change in Child CHQ General Health Perception subscale score from baseline, 6 months, 12 months to 24 months [baseline, 6 months, 12 months and 24 months]

      Quality of life: Child Health Questionnaire - Parent Form 50 (CHQ-PF50) is a parent proxy measure of children's physical and psychological wellbeing, with 50 items grouped into 12 multi-item subscales. Its Chinese version has been shown to have good psychometric properties in local Chinese children

    Secondary Outcome Measures

    1. Change in Child SDQ Totally Difficulty score from baseline, 6 months, 12 months to 24 months [baseline, 6 months, 12 months and 24 months]

      Strength and Difficulties Questionnaire (SDQ) is a 25-item parent-completed questionnaire measuring children's behavioral issues. The SDQ, with 5 subscales, has been translated into traditional Chinese and tested with satisfactory reliability and validity in local children.

    2. Change in Child telomere length from baseline to 24 months [baseline and 24 months]

      Telomere length will be measured by the method adapted from that originally published by Cawthon. For each sample, the telomere length will be represented by the relative ratio of the telomere repeat copy number (T) to the single copy gene 36BA copy number (S). The T/S ratio will be determined by quantitative polymerase chain reaction (qPcR) using a 7900HT Thermocycler (Applied Biosystems).

    3. Change in Parental allostatic load index from baseline, 6 months, 12 months to 24 months [baseline, 12 months and 24 months]

      A review of literature has identified a set of physiological parameters that can reflect allostatic load and yet be conveniently measured, including blood pressure, heart rate, body-mass-index, waist-to-hip ratio, lipid profile, fasting glucose and glycosylated haemoglobin. An index score of allostatic load will be calculated by summing the number of parameters that fall into the "highest" risk quartile defined by local clinical practice guidelines

    4. Change in Parental SF-12v2 HRQOL scores from baseline, 6 months, 12 months to 24 months [baseline, 6 months, 12 months and 24 months]

      The SF-12 Health Survey-Version 2 (SF-12v2) is a 12-item quality of life assessment instrument that covers 8 subscales. The Chinese version of SF-12v2 has been validated and normed in local Chinese population

    5. Change in Parental DASS Stress subscale score from baseline, 6 months, 12 months to 24 months [baseline, 6 months, 12 months and 24 months]

      Depression Anxiety Stress Scale (DASS) has 3 subscales, each with 7 items rating the severity/frequency of symptoms of stress, anxiety and depression respectively. DASS also has well-established psychometric properties and been validated in Chinese population.

    Other Outcome Measures

    1. Parental PHQ-9-score, DASS Depression and Anxiety subscale score [6 months]

      Depression Anxiety Stress Scale (DASS) has 3 subscales, each with 7 items rating the severity/frequency of symptoms of stress, anxiety and depression respectively. DASS also has well-established psychometric properties and been validated in Chinese population. In addition, Patient Health Questionnaire - 9 (PHQ-9) will be used to screen for depression in parents. The Chinese version of PHQ-9 has been validated and used in previous local studies.

    2. Family disharmony measured by FHS-5 [6 months]

      The Chinese version of Family Harmony Scale - 5 (FHS-5) will be used to measure family harmony.

    3. Child physical assault and neglect potential measured by the Physical Assault and Neglect subscale of the CTSPC [6 months]

      Parental risk of physically abusing and neglecting children will also be assessed with the Child Physical Assault and Neglect subscale of the Parent Child Conflict Tactics Scale (CTSPC).

    4. Authoritative parenting style measured by the Authoritative Parenting Style subscale of the PSDQ [6 months]

      Parenting style will be assessed using the Authoritative Parenting Style subscale of the Parenting Style and Dimension Questionnaire (PSDQ).

    5. Neighbourhood cohesion measured by NCES [6 months]

      The Chinese version of Neighborhood Collective Efficacy Scale (NCES) is a 10-item scale, with five items each on informal social control and social cohesion.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    6 Years to 16 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Family monthly household income does not exceed 75% of Hong Kong's median monthly household income

    • At least one parent and one child aged 6 to 16 years of the same family have given consent to participate in the main cohort study

    Exclusion Criteria:
    • Parents cannot speak or read Chinese;

    • Children were born prematurely and/or with a congenital deformity; and

    • Neither parent is the primary caregiver of the child.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 The University of Hong Kong Hong Kong Hong Kong

    Sponsors and Collaborators

    • The University of Hong Kong

    Investigators

    • Principal Investigator: Esther Yee Tak Yu, The University of Hong Kong

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    The University of Hong Kong
    ClinicalTrials.gov Identifier:
    NCT03185273
    Other Study ID Numbers:
    • UW16-145
    First Posted:
    Jun 14, 2017
    Last Update Posted:
    Mar 3, 2020
    Last Verified:
    Mar 1, 2020
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No

    Study Results

    No Results Posted as of Mar 3, 2020