- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02877719
The Effect of Poverty on Psychological Well-being of Children
August 19, 2016 updated by: The University of Hong Kong
The Effect of Poverty and Income Disparity on the Psychological WellBeing of Hong Kong Children
The aim of this study is to explore the impacts of poverty and income disparity on the psychological well-being of Hong Kong Chinese children.
Study Overview
Detailed Description
It is well documented that poverty has a negative impact on the physiological well-being of children in the West.
There is an imperative need for health care professionals to develop and evaluate interventions to promote the psychological wellbeing of children living in poverty.
First, however, it is crucial to assess and understand how the impact of poverty, in particular the impact of income disparity, affects the psychological wellbeing of Hong Kong children before any intervention to promote it can be planned, developed, or evaluated.
Unfortunately, while much public concern about poverty has concentrated on children's physical development, the impact of poverty and income disparity on their psychological well-being remains relatively underexplored.
Because the cultural context in which they live is drastically different from that of Western children, the way that Chinese children view the nature and meaning of poverty, as well as their responses to it and to any psychosocial interventions, will in all likelihood differ considerably from those of Western children.
Hence, the aim of this study is to explore the impacts of poverty and income disparity on the psychological well-being of Hong Kong Chinese children.
Study Type
Observational
Enrollment (Actual)
1725
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Hong Kong SAR, China
- The University of Hong Kong
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
10 years to 13 years (Child)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Hong Kong Chinese pupils from Grades 5 and 6 of the elementary schools in Hong Kong
Description
Inclusion Criteria:
- Hong Kong Chinese pupils from Grades 5 and 6 of the elementary schools in Hong Kong
- be able to read Chinese and speak Cantonese
- had to live and go to school in the same district
Exclusion Criteria:
- Children with chronic illness or identified cognitive and learning problems
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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Children from low-income families
Children from low-income families were invited to fill in a set of questionnaires.
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Participants were asked to respond to the Chinese version of the Center for Epidemiologic Studies Depression Scale for Children, the Rosenberg self-esteem scale, and the Pediatric Quality of Life Inventory.
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Children from high income families
Children from high-income families were invited to fill in a set of questionnaires.
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Participants were asked to respond to the Chinese version of the Center for Epidemiologic Studies Depression Scale for Children, the Rosenberg self-esteem scale, and the Pediatric Quality of Life Inventory.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Levels of quality of life at baseline
Time Frame: baseline
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The quality of life of the participants will be measured by the Chinese version of the Pediatric Quality of Life Inventory (PedsQL).
It has 23 items which are grouped into 4 subscales.
They are physical functioning (8 items), emotional functioning (5 items), social functioning (5 items) and school functioning (5 items).
Participants were asked to rate how often they had experienced problems over the past month on a scale from 0 to 4. Higher scores indicate better quality of life.
Participants will be asked to respond to the Chinese version of the Pediatric Quality of Life Inventory (PedsQL) at baseline.
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baseline
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Levels of self-esteem at baseline
Time Frame: baseline
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The self-esteem of the participants will be measured by the Chinese version of the Rosenberg Self-esteem Scale (RSES).
It contains 10 items which are measured on a 4-point Likert scale.
Each item is rated from 1 to 4. The higher scores represent the higher levels of global self-esteem of children.
Participants will be asked to respond to the Chinese version of the Rosenberg Self-esteem Scale (RSES) at baseline.
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baseline
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Number of depressive symptoms at baseline
Time Frame: baseline
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The number of depressive symptoms of the participants will be measured by the Chinese version of The Center for Epidemiologic Studies Depression Scale for Children (CES-DC).
It consists of 20 items that are measured on a 4-point Likert scale in relation to the experience of last week.
Each item is rated from 0 to 3. The higher scores of CES-DC indicate the high numbers of depressive symptoms.
The cutoff of this scale is 16, which indicates the children currently experiencing a significant level of depressive symptoms Participants will be asked to respond to the Chinese version of the Center for Epidemiologic Studies Depression Scale for Children (CES-DC) at baseline.
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baseline
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Ho Cheung William Li, The University of Hong Kong
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
February 1, 2012
Primary Completion (Actual)
January 1, 2013
Study Completion (Actual)
January 1, 2013
Study Registration Dates
First Submitted
August 16, 2016
First Submitted That Met QC Criteria
August 19, 2016
First Posted (Estimate)
August 24, 2016
Study Record Updates
Last Update Posted (Estimate)
August 24, 2016
Last Update Submitted That Met QC Criteria
August 19, 2016
Last Verified
August 1, 2016
More Information
Terms related to this study
Other Study ID Numbers
- UW12-237
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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