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Effectiveness of Musical Training in Children From Low Income Families

30 mai 2018 mis à jour par: The University of Hong Kong

Effectiveness of Musical Training in the Improvement of Psychological Well-being and Quality of Life of Children From Low Income Families

This study aims to examine the effectiveness of musical training in promoting happiness and quality of life of preschool children from low-income families.

Participants in the experimental group will attend a weekly 1-hour musical training lesson for 12 weeks conducted by the Music Children Foundation. While participants in the waitlist control group received the same training after the experimental group had completed the intervention.

Aperçu de l'étude

Statut

Complété

Les conditions

Intervention / Traitement

Description détaillée

Children from low income families generally suffer from hard conditions,such as poor living conditions, inadequate nutrition, and delay in accessing health care services. Such problems may made children suffer from developmental problems and malnutrition and to have a lower level of intelligence and difficulties in language comprehension, which may not only have profound impacts on children's physical well-being, but on their psychological well-being as well. Musical training is considered to have potential for promoting psychological well-being among children mostly because music is found to be important to a child's early psychological development. A growing number of educators and researchers suggest that, of all the stages of life, infancy may be the time when music has the most important impact on an individual. Babies hear language long before they are able to comprehend it. The quality and the quantity of what is unconsciously absorbed in infancy relates directly to later development. Musical training has been used for various purposes such as improving language development, self-expression, memory skills, concentration, social interaction, fine motor skills, listening, problem-solving, teamwork, goal setting, and coordination. More importantly, when a child learns to sing and play music, other areas of development - creativity, family bonding, self-esteem, confidence, emotional development - are also positively impacted.

Nevertheless, although musical training is popular and is considered to be a beneficial intervention in the promotion of psychological well-being, longitudinal studies that examine the efficacy of music-making in children from low-income families are limited. Importantly, there is to date no study that examines the effects of musical training on enhancing the psychological well-being among these children. There is an imperative need for rigorous empirical scrutiny of the effectiveness of musical training in promoting the psychological well-being of children from low-income families. Therefore, the aim of this study is to examine the effectiveness of musical training in promoting happiness and quality of life of preschool children from low-income families.

Type d'étude

Interventionnel

Inscription (Réel)

171

Phase

  • N'est pas applicable

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

      • Hong Kong, Chine
        • The University of Hong Kong

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

3 ans à 6 ans (Enfant)

Accepte les volontaires sains

Non

Sexes éligibles pour l'étude

Tout

La description

Inclusion Criteria:

  • be aged from 3 to 6 years,
  • be able to communicate in Cantonese,
  • be from low-income families; that is, less than half the median monthly household income or recipients of Comprehensive Social Security Assistance.

Exclusion Criteria:

  • children who had studied or were studying (at the time of the intervention) a musical instrument
  • children who were receiving other community services at the time of the intervention,
  • children with chronic illness or identified cognitive and learning problems.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Soins de soutien
  • Répartition: Non randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Seul

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Experimental
Participants in the experimental group will receive weekly one-hour lessons on musical training for 12 weeks, conducted by the Music Children Foundation. The Music Children Foundation is a non-governmental organization established by a group of professional musicians with the objective of transforming children's lives and instils positive values in the entire community through music. It aims to provide free musical training to low-income children and children with chronic diseases, including those with Down's syndrome, mucopolysaccharidoses, skeletal dysplasia and visual impairment.
The subjects in the experimental group will receive weekly one-hour lessons on musical training for 12 weeks, conducted by the Music Children Foundation.
Aucune intervention: Wait-list control group
Participants in the waitlist control group will receive the same training after the experimental group had completed the intervention.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
The change of quality of life from baseline at 12 weeks follow-up between intervention and control group.
Délai: 12 weeks follow-up

The subjects' quality of life will be assessed at 12 weeks after starting the intervention, using the Chinese version of the Paediatric Quality of Life Inventory 4.0 Generic Core Scale (PedsQL 4.0).

The parents will be asked to fill in this questionnaire for their children. The PedsQL is designed to measure children's healthrelated quality of life. It comprises 23 items rated on a 5-point Likert scale. These items are categorised into four domains: physical functioning (eight items), emotional functioning (five items), social functioning (five items) and school functioning (five items). The total possible range of scores is from 0 to 100, with higher scores indicating better quality of life.

12 weeks follow-up

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Quality of life at baseline between intervention and control group.
Délai: baseline
The subjects' quality of life will be assessed at the baseline, using the Chinese version of the Paediatric Quality of Life Inventory 4.0 Generic Core Scale (PedsQL 4.0) The parents will be asked to fill in this questionnaire for their children. The PedsQL is designed to measure children's healthrelated quality of life. It comprises 23 items rated on a 5-point Likert scale. These items are categorised into four domains: physical functioning (eight items), emotional functioning (five items), social functioning (five items) and school functioning (five items). The total possible range of scores is from 0 to 100, with higher scores indicating better quality of life.
baseline
Happiness at baseline between intervention and control group.
Délai: baseline

The subjects' happiness will be assessed 12 weeks after starting the intervention, using the Visual Analog Scale.

The children will be asked to rate their average level of happiness in the last week from zero (not happy or sad) to ten (extremely happy), with higher scores representing higher level of happiness.

baseline
The change of happiness from baseline at 12 weeks follow-up between intervention and control group.
Délai: 12 weeks follow-up

The subjects' happiness will be assessed 12 weeks after starting the intervention, using the Visual Analog Scale.

The children will be asked to rate their average level of happiness in the last week from zero (not happy or sad) to ten (extremely happy), with higher scores representing higher level of happiness.

12 weeks follow-up

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Les enquêteurs

  • Chercheur principal: Ho Cheung William Li, The University of Hong Kong

Publications et liens utiles

La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

1 mars 2017

Achèvement primaire (Réel)

30 novembre 2017

Achèvement de l'étude (Réel)

28 février 2018

Dates d'inscription aux études

Première soumission

3 mai 2016

Première soumission répondant aux critères de contrôle qualité

3 mai 2016

Première publication (Estimation)

5 mai 2016

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

1 juin 2018

Dernière mise à jour soumise répondant aux critères de contrôle qualité

30 mai 2018

Dernière vérification

1 mai 2018

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • PhD_2

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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