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

Status

Completed

Conditions

Intervention / Treatment

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

      • Hong Kong SAR, China
        • The University of Hong Kong

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
Children from low-income families
Children from low-income families were invited to fill in a set of questionnaires.
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.
Children from high income families
Children from high-income families were invited to fill in a set of questionnaires.
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.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Levels of quality of life at baseline
Time Frame: baseline
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.
baseline

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Levels of self-esteem at baseline
Time Frame: baseline
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.
baseline
Number of depressive symptoms at baseline
Time Frame: baseline
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.
baseline

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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

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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