The Hong Kong Children's Hospital
Hong Kong
NCT Number: NCT05202925
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.
Looking for future studies?
Notify Me7 year–16 year
All sexes
Interventional
Not applicable
Hong Kong
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:
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
a weekly 45-minute lesson, one-to-one musical training
Time frame: at baseline before the start of the intervention
the proportion of subjects who are eligible and invited and consent to participate.
Time frame: at baseline and 12 months after starting the intervention
The proportion of subjects who complete the questionnaires and assessments at baseline and 12 months after starting the intervention
Time frame: at baseline and 12 months after starting the intervention
The proportion of subjects who complete the whole intervention from baseline to 12 months.
Time frame: at baseline and 12 months after starting the intervention
Measured by the Test of Nonverbal Intelligence, 4th edition (TONI-4)
Time frame: at baseline and 12 months after starting the intervention
Measured by the Digit Span
Time frame: at baseline and 12 months after starting the intervention
Measured by the Children's Color Trails Test (CCTT)
Time frame: at baseline and 12 months after starting the intervention
Measured by the Children's Color Trails Test (CCTT)
The Hong Kong Polytechnic University
Other
Feasibility Study of a Musical Training Program in Improving the Neurocognitive Functioning of Children Surviving Brain Tumours
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT05584930
Agranulocytosis, Cancer Childhood
Angers, France
View Trial DetailsNCT03544190
Cancer Childhood, Neoplasms
Hong Kong
View Trial DetailsNCT07630831
Cancer Childhood, Neoplasms
Los Angeles, California, United States
View Trial DetailsNCT07201038
Cancer Childhood, Neoplasms
Cambridge, United Kingdom
View Trial Details