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CompletedNCT05346965Updated Aug 1, 2023

Musical Training to Enhance Resilience in Children From Low-income Families

An interventional study of Musical training in Resilience, sponsored by Chinese University of Hong Kong. Completed at 1 site in Hong Kong. Open to participants aged 8 Years to 12 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-08-01.

Sponsored by Chinese University of Hong Kong · Not applicable, Interventional, and Supportive care

Phase
Not applicable
Study type
Interventional
Enrollment
64
Allocation
Randomized
Ages
8 Years to 12 Years
Sex
All
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Study summary

Child poverty is a prominent global health issue owing to its detrimental impact on a child's physical and psychosocial well-being. Nearly 356 million children lived in extreme poverty globally before the pandemic and this is estimated to worsen significantly. children growing up in poverty are more vulnerable to its effect and have an increased risk of psychosocial and developmental problems than children from affluent families. The impact of poverty is not only immediate during childhood but can persist into adulthood. Previous studies have shown that Chinese children from low-income families reported significantly higher levels of depressive symptoms, lower levels of self-esteem, quality of life, and life satisfaction than children from affluent families.

Recent studies have revealed the promising effects of musical training to promote psychological well-being among children and adolescents and paediatric brain tumour survivors, improving psychosocial skills of children with autism, to enhance the quality of life and psychological health by promoting positive emotions and cognitive and social development.

Promoting the psychological health of school-aged children from low-income families through enhancing their resilience has received limited research attention. Additionally, there is a lack of intervention studies to promote resilience in school-aged children from low-income families. This proposed research, therefore, aims to conduct a pilot randomised controlled trial to determine the feasibility, acceptability and preliminary effects of a musical training programme in enhancing resilience and self-esteem, reducing depressive symptoms and improving the quality of life among children from low-income families.

The findings from the study could inform the policymakers and healthcare professionals in health services design and the importance of advocating the psychological needs of children from low-income families by providing adequate community resources and support. If the programme demonstrates its effectiveness in promoting resilience and self-esteem among children from low-income families, further implementation could be done to maintain its sustainability in the community. Most importantly, the programme may potentially enhance the resilience of the vulnerable children from low-income families to combat poverty and hence break the intergenerational transmission of poverty.

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Conditions studied

  • Resilience
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In context

Lead sponsor

Chinese University of Hong Kong is the lead sponsor of 1,419 studies on the registry; 487 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
8 Years to 12 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Chinese children aged between 8-12 years
  • able to read Chinese and communicate in Cantonese
  • from low-income families, that is, less than half the median monthly household income or recipients of Comprehensive Social Security Assistance

Exclusion criteria

Exclusion Criteria:

  • children who are currently receiving or had received musical training before the study
  • children have chronic diseases, cognitive and learning difficulties
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Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
64 participants (actual)

Study arms

  • Experimental
    Musical training programme

    Participants in the experimental group received a weekly 1-hour musical training lesson for 6 months delivered by professionally qualified musicians. The participants will be assigned a particular musical instrument to learn, and this is based on their interests as well as their capabilities (i.e., fine motor skills), The training will begin at the lowest level (hitting simple notes) and end at the highest level (able to play an entire song).

    Behavioral: Musical training

  • Active comparator
    Wait-list control group

    To ensure equity of access to potentially effective intervention (i.e. musical training programme), participants in the wait-list control group will receive the same musical training programme as participants in the intervention group after the completion of all assessments.

    Behavioral: Musical training

Interventions

  • BehavioralMusical training

    The musical training intervention comprised songs, rhythm and visual creativity to encourage the children to experience music-making as fun.

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What researchers measure

Primary outcomes

  1. Resilience - Resilience Scale for Children

    Children's resilience will be measured by the Resilience Scale for Children- 10 (RS10) which was developed based on the Resilience Scale originally developed by Wagnild and Young. Total scores ranging from 10 to 40, with higher scores indicate higher levels of resilience.

    Time frame: 6-month follow-up

Secondary outcomes

  1. Level of self-esteem - Rosenberg self-esteem scale

    Levels of self-esteem will be measured by the Chinese version of the Rosenberg self-esteem scale (RSES), which is a tool designed to measure the global self-esteem of children and adolescents. Total scores ranging from 10 to 40, with higher scores indicate higher levels of self-esteem.

    Time frame: Baseline, and 6-month follow-up

  2. Depressive symptoms - Center for Epidemiological Studies Depression Scale

    The Chinese version of the Center for Epidemiological Studies Depression Scale for Children (CES-DC) will be used to assess the participants' depressive symptoms. Total scores ranging from 0 to 60, with higher scores indicate higher level of depressive symptoms.

    Time frame: Baseline, and 6-month follow-up

  3. Quality of life - Pediatric Quality of Life Inventory 4.0 Generic Core

    The Chinese version of the Pediatric Quality of Life Inventory 4.0 Generic Core Scale (PedsQL 4.0) will be used to assess children's quality of life. Total scores ranging from 0 to 100, with higher scores represent better quality of life.

    Time frame: Baseline, and 6-month follow-up

  4. Acceptability and satisfaction

    Acceptability and satisfaction will be determined upon the completion of the intervention using a short one-to-one semi-structured interview, which aims to explore the perception of the children and their parents towards the musical training programme; both children and parents will be asked to comment on their experience and feelings of the program; and to provide recommendation for improvement of the programme.

    Time frame: 6-month follow-up

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Study locations

1 site
  • The Chinese University of Hong Kong
    Hong Kong, Hong Kong
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 1, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05346965
Lead sponsor
Chinese University of Hong Kong
Collaborators
Alice Ho Miu Ling Nethersole Hospital
Responsible party
Cheung Tan (Principal Investigator, Chinese University of Hong Kong) — Principal investigator
First posted
Apr 26, 2022
Start date
May 16, 2022
Primary completion
Jul 3, 2023
Completion
Jul 3, 2023
Last update
Aug 1, 2023

Study contacts

Ankie Tan Cheung, PhD
principal investigator · Chinese University of Hong Kong

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jul 2023. You cannot join it, but the record below documents what was studied.

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