Skip to content

Musical Training Programme to Improve Neurocognitive Functioning of Children Surviving Brain Tumours

Feasibility Study of a Musical Training Program in Improving the Neurocognitive Functioning of Children Surviving Brain Tumours

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05202925
Enrollment
40
Registered
2022-01-24
Start date
2021-10-01
Completion date
2024-02-15
Last updated
2024-07-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Brain Tumor, Cancer Childhood

Brief summary

We aim to conduct a feasibility study to determine the feasibility and suitability of implementing a musical training program for children surviving brain tumours. This study will demonstrate the feasibility of implementing a musical training program in improving the neurocognitive functioning of surviving brain tumours.

Detailed description

Brain tumour is the second most common childhood cancer in Hong Kong. Evidence shows that cancer and its treatments have long-term and lasting adverse effects on the neurocognitive functioning of paediatric brain tumour survivors, including the impairment of intellectual development and deficits in attention, working memory, processing speed and executive functions. There has been an increase in the use of musical training to promote the neuro-rehabilitation of patients suffering from stroke and Parkinson's disease, and to improve reading skills and academic achievement in young poor readers, and to enhance children's cognitive development. We conducted a randomized controlled trial (RCT) from 2017 to 2018 to examine the effectiveness of musical training on psychological outcomes and quality of life in Chinese paediatric brain tumour survivors. The results showed that participants who received a weekly 45-min lesson on musical training for 52 weeks (intervention group) reported statistically significant fewer depressive symptoms, higher levels of self-esteem, and better quality of life than those who received placebo intervention (control group) at 12-month demonstrating the effectiveness of musical training intervention. Nevertheless, it is unclear whether musical training can also be used to improve neurocognitive functioning, in particular the attention, processing speed, and executive functions of children surviving brain tumours. The overall aim of this proposed study will be to assess the feasibility of a musical training program in improving the neurocognitive functioning of children surviving brain tumours. The objectives of this feasibility study are as follows: 1. To ascertain the feasibility of recruitment and data collection in the outpatient clinic of the Hong Kong Children's Hospital; 2. To assess the response and retention rates of the study; 3. To examine the content of the proposed musical training program for its appropriateness, comprehensiveness and duration to the target participants; 4. To evaluate the appropriateness and feasibility of using various assessment tools in measuring the intelligence, attention, processing speed and executive functions of the paediatric brain tumour survivors; and 5. To assess any changes in neurocognitive functioning of children surviving brain tumours after receiving musical training for 52 weeks.

Interventions

a weekly 45-minute lesson, one-to-one musical training

Sponsors

Health and Medical Research Fund
CollaboratorOTHER_GOV
The Hong Kong Polytechnic University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
7 Years to 16 Years
Healthy volunteers
No

Inclusion criteria

1. children who have completed cancer treatment at least 2 months previously; 2. aged between 7 and 16 years, 3. able to speak Cantonese and read Chinese, and 4. those who have not undertaken any musical training following their cancer diagnosis.

Exclusion criteria

1\. those survivors with evidence of cancer recurrence or second malignancy in their medical records

Design outcomes

Primary

MeasureTime frameDescription
Recruitment rate of the studyat baseline before the start of the interventionthe proportion of subjects who are eligible and invited and consent to participate.
Response rate of the studyat baseline and 12 months after starting the interventionThe proportion of subjects who complete the questionnaires and assessments at baseline and 12 months after starting the intervention
Retention rate of the studyat baseline and 12 months after starting the interventionThe proportion of subjects who complete the whole intervention from baseline to 12 months.

Secondary

MeasureTime frameDescription
Nonverbal intelligence scores of the subjectat baseline and 12 months after starting the interventionMeasured by the Test of Nonverbal Intelligence, 4th edition (TONI-4)
Executive functions scores of the subjectat baseline and 12 months after starting the interventionMeasured by the Children's Color Trails Test (CCTT)
Attention scores of the subjectat baseline and 12 months after starting the interventionMeasured by the Digit Span
Processing speed scores of the subjectat baseline and 12 months after starting the interventionMeasured by the Children's Color Trails Test (CCTT)

Countries

Hong Kong

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 5, 2026