Music Program for Hong Kong Adolescents: Improving Emotion Regulation and Reducing Depression, Anxiety, and Loneliness

Sponsor
The University of Hong Kong (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06147297
Collaborator
The University of Queensland (Other), The Hong Kong Polytechnic University (Other), Health and Medical Research Fund (Other)
100
1
2
20.5
4.9

Study Details

Study Description

Brief Summary

This study is a clinical trial that aims to test and validate a music-based program called "Tuned In" in helping adolescents in Hong Kong improve their mental well-being. The researchers want to find out if the program can help participants enhance their ability to regulate their emotions, reduce mood symptoms and feelings of loneliness.

Participants in the study will be randomly assigned to either the group that receives the program right away (intervention group) or the group that waits for four weeks before receiving the program (wait list group). They will take part in a group-based weekly program for four weeks. Additionally, they will be asked to complete questionnaires before and after the program to see if there are any changes in their mental well-being. The program will be delivered by a facilitator with a psychology background, and a registered music therapist.

By addressing the gaps in mental health interventions for young people in Hong Kong, this study aims to contribute to the development of effective strategies to support their emotional well-being.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Tuned In
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
100 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Intervention group: Receive the music-based program, and complete the survey before- and after- the program. Waitlist group: Invited to complete the survey before- and after the 4-week waiting period. Then the waitlist group will also be offered the program, and invited to complete an optional post-program survey.Intervention group: Receive the music-based program, and complete the survey before- and after- the program. Waitlist group: Invited to complete the survey before- and after the 4-week waiting period. Then the waitlist group will also be offered the program, and invited to complete an optional post-program survey.
Masking:
Double (Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Using Music to Promote Young People's Emotion Regulation and Reduce Their Depressive and Anxious Symptoms and Loneliness: A Pilot Randomised Controlled Trial
Anticipated Study Start Date :
Dec 1, 2023
Anticipated Primary Completion Date :
Aug 17, 2025
Anticipated Study Completion Date :
Aug 17, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention group

Receive the music-based program once a week for 4 weeks, each session is 60 to 90 minutes, and participants will complete the survey before- and after- the program.

Behavioral: Tuned In
The Tuned In programme is based on Russell's (1980) circumplex model of emotion, which categories emotions along the two dimensions of valence and arousal. Through psychoeducation and group discussions, participants in the programme first learn how to categorise their emotions in terms of intensity (i.e., arousal level) and positivity (i.e., valence). They then reflect on and develop a list of songs that they relate to personally and use them to increase or decrease the intensity and positivity of their emotions. In other words, the participants practise monitoring their emotional state and use music to help them modify how they feel. The programme will be conducted by a facilitator with a psychology background, and a registered music therapist.

No Intervention: Wait-list group

Complete the survey before- and after the 4-week waiting period. Then the waitlist group will also be offered the program, and invited to complete an optional post-program survey

Outcome Measures

Primary Outcome Measures

  1. Emotion Regulation Skills [Questionnaires will be administered before the start of the program, and immediately after the program (intervention group) or after 4 weeks of wait period (wait-list group)]

    To assess difficulties, strategies, and confidence in emotion regulation, we will use the Emotion Regulation Questionnaire (Liu et al., 2015), Difficulties in Emotion Regulation scale, and select items from Dingle and Carter's (2017) program evaluation tool.

Secondary Outcome Measures

  1. Mood symptoms [Questionnaires will be administered before the start of the program, and immediately after the program (intervention group) or after 4 weeks of wait period (wait-list group)]

    The Depression Anxiety Stress Scale-21 (Moussa et al., 2001; DASS-21) will be used to measure mood symptoms

  2. Loneliness [Questionnaires will be administered before the start of the program, and immediately after the program (intervention group) or after 4 weeks of wait period (wait-list group)]

    The Hong Kong version of the De Jong Gierveld Loneliness Scale (Leung et al., 2008) will be used to measure loneliness

Other Outcome Measures

  1. Anhedonia [Questionnaires will be administered before the start of the program, and immediately after the program (intervention group) or after 4 weeks of wait period (wait-list group)]

    The Chinese version of the Snaith-Hamilton-Pleasure scale (Liu et al., 2012) will be used to measure anhedonia.

  2. Program acceptability and feasibility [Questionnaire will be administered immediately after the program]

    Furthermore, we plan to examine the acceptability of the program with the Hong Kong adolescents. This will be done using a combination of quantitative and qualitative approaches. Satisfaction ratings will be collected from the participants, on a 7-point Likert scale. The questions will be on the perceived usefulness of the program, the level of interest in the program, the likelihood of them recommending the program to other adolescents, and the likelihood of them to continue using music as an emotion regulatory strategy in the future (Dingle et al., 2016). We will also use open-ended questions to obtain feedback from the participants on their experiences of the program, and ask for suggestions for improvements for a future RCT. Furthermore, as feasibility indicators, we will also record the recruitment rate and dropout rate of this trial.

Eligibility Criteria

Criteria

Ages Eligible for Study:
16 Years to 19 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • self-report as having problems with low mood, anxiety or loneliness

  • score 3 or above on the General Health Questionnaire (GHQ-12), which indicates psychological distress.

Contacts and Locations

Locations

Site City State Country Postal Code
1 The University of Hong Kong Hong Kong Hong Kong

Sponsors and Collaborators

  • The University of Hong Kong
  • The University of Queensland
  • The Hong Kong Polytechnic University
  • Health and Medical Research Fund

Investigators

  • Principal Investigator: Yuan Cao, The University of Hong Kong

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
The University of Hong Kong
ClinicalTrials.gov Identifier:
NCT06147297
Other Study ID Numbers:
  • EA230395
  • 10211636
First Posted:
Nov 27, 2023
Last Update Posted:
Nov 27, 2023
Last Verified:
Oct 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by The University of Hong Kong
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 27, 2023