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CompletedNCT07393581GMT2025Updated Feb 6, 2026

Group Music Therapy for Emotional Well-Being and Social Connectedness

An interventional study of Active Group Music Therapy and Receptive Group Music Therapy in Anxiety, Emotional Well-Being and Social Connectedness, sponsored by Chinese University of Hong Kong. Completed at 1 site in China. Open to participants aged 18 Years to 26 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-02-06.

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

From the registry’s dates

  • Registered 2 years 8 months after the study started (first participant enrolled May 2023, registered Jan 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
120
Allocation
Randomized
Ages
18 Years to 26 Years
Sex
All
01

Study summary

This randomized controlled trial evaluated whether two formats of group music therapy can improve emotional well-being, self-rated health, and social connectedness among undergraduate students living in urban areas in China. A total of 120 students were randomly assigned to one of three conditions: (1) active group music therapy, (2) receptive group music therapy, or (3) a waitlist control group.

Both music therapy programs were delivered in person over 6 weeks, with one 60-minute session per week facilitated by trained music therapists. The active format emphasized participatory music-making (e.g., singing, rhythmic activities, and group improvisation), while the receptive format focused on guided music listening and reflection.

Participants completed self-report questionnaires at baseline and immediately after the 6-week period assessing positive and negative affect, anxiety symptoms, general health, and perceived social connectedness. The study examined whether the two music therapy approaches led to improvements compared with the waitlist control condition.

Read the detailed description

This study used a parallel-group randomized controlled design to examine the effects of two structured formats of group music therapy on emotional well-being, anxiety symptoms, self-rated health, and social connectedness among undergraduate students in urban China. Participants were recruited through university announcements and campus-based advertisements. Eligible participants provided informed consent and completed baseline assessments before being randomly allocated to one of three conditions: active group music therapy, receptive group music therapy, or a waitlist control group.

The intervention period lasted 6 weeks. Participants assigned to either music therapy condition attended weekly in-person group sessions of approximately 60 minutes in small groups (10-15 participants). Sessions were delivered by trained music therapists using standardized protocols to ensure structural equivalence across conditions. The active group music therapy format emphasized participatory music-making (e.g., group singing, rhythmic call-and-response, body percussion, and collaborative musical activities) and included brief guided group discussion at the end of each session. The receptive group music therapy format emphasized guided music listening, music-assisted imagery/visualization, reflective writing or moderated discussion, and relaxation/breathing exercises.

Participants in the waitlist control condition did not receive any intervention during the 6-week study period but completed the same baseline and post-intervention assessments as the intervention groups. After completion of the study, waitlist participants were offered the option to attend one group music therapy session.

All outcomes were assessed using self-report measures administered at baseline and immediately after the 6-week period.

02

Conditions studied

  • Anxiety
  • Emotional Well-Being
  • Social Connectedness

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Keywords

  • group music therapy
  • active music therapy
  • receptive music therapy
03

In context

Anxiety Disorders

4,874 studies on the registry are indexed under Anxiety Disorders; 1,394 are open to participants now.

This study's enrollment of 120 is above the median of 80 across 4,180 interventional studies indexed under Anxiety Disorders.

Browse Anxiety Disorders studies →

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.

04

Who can participate

Ages eligible
18 Years to 26 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

Undergraduate university students aged 18 to 26 years

Living in an urban area in China

Able to attend weekly in-person group sessions for 6 weeks

Provided written informed consent

Exclusion criteria

Exclusion Criteria:

Self-reported severe active clinical diagnosis

05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
120 participants (actual)

Study arms

  • Experimental
    Active Music Therapy (MT-A)

    Weekly in-person active group music therapy sessions for 6 weeks (60 minutes per session; groups of 10-15 participants) facilitated by trained music therapists. Sessions included group singing, rhythmic improvisation using body percussion or simple instruments, collaborative musical games, and brief guided group discussion.

    Behavioral: Active Group Music Therapy

  • Experimental
    Receptive Music Therapy (MT-R)

    Weekly in-person receptive group music therapy sessions for 6 weeks (60 minutes per session; groups of 10-15 participants) facilitated by trained music therapists. Sessions included guided music listening, music-assisted imagery/visualization, reflective writing or moderated discussion, and breathing/relaxation exercises.

    Behavioral: Receptive Group Music Therapy

  • No intervention
    Waitlist Control

    Participants received no sessions during the 6-week study period and completed baseline and post-intervention assessments. After study completion, participants were offered the option to attend one group music therapy session.

Interventions

  • BehavioralActive Group Music Therapy

    Active group music therapy delivered in person once weekly for 6 weeks (60 minutes per session). Activities included group singing, rhythmic call-and-response, body percussion, simple percussion instruments, and collaborative musical games.

  • BehavioralReceptive Group Music Therapy

    Receptive group music therapy delivered in person once weekly for 6 weeks (60 minutes per session). Activities included guided music listening, music-assisted imagery/visualization, reflective writing or moderated discussion, and breathing/relaxation exercises.

06

What researchers measure

Primary outcomes

  1. Anxiety symptoms (GAD-7 total score)

    Anxiety symptoms assessed using the Generalized Anxiety Disorder 7-item scale (GAD-7). Higher scores indicate greater anxiety severity.

    Time frame: Baseline (pre-intervention) and immediately post-intervention (6 weeks)

Secondary outcomes

  1. Positive affect (I-PANAS-SF Positive Affect subscale)

    Positive affect assessed using the International Positive and Negative Affect Schedule Short Form (I-PANAS-SF), Positive Affect subscale. Higher scores indicate higher positive affect.

    Time frame: Baseline (pre-intervention) and immediately post-intervention (6 weeks)

  2. Negative affect (I-PANAS-SF Negative Affect subscale)

    Negative affect assessed using the International Positive and Negative Affect Schedule Short Form (I-PANAS-SF), Negative Affect subscale. Higher scores indicate higher negative affect.

    Time frame: Baseline (pre-intervention) and immediately post-intervention (6 weeks)

  3. Self-rated general health (SF-36 General Health subscale)

    General health assessed using the Short Form Health Survey (SF-36), General Health subscale. Scores are transformed to a 0-100 scale, with higher scores indicating better perceived health.

    Time frame: Baseline (pre-intervention) and immediately post-intervention (6 weeks)

  4. Social connectedness (Social Connectedness Scale-Revised)

    Social connectedness assessed using the Social Connectedness Scale-Revised (SCS-R), Social Connectedness subscale. Higher scores indicate stronger perceived social connectedness.

    Time frame: Baseline (pre-intervention) and immediately post-intervention (6 weeks)

07

Study locations

1 site
  • Yangzhou University
    Yangzhou, Jiangsu 225000, China
08

References and documents

Individual participant data

Plan to share: Yes — De-identified individual participant data and study materials will be made publicly available via the Open Science Framework (OSF).

Supporting information: Study protocol, Analytic code

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 6, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07393581
Lead sponsor
Chinese University of Hong Kong
Collaborators
Yangzhou University
Responsible party
Ling Yang (Principal Investigator, Chinese University of Hong Kong) — Principal investigator
First posted
Feb 6, 2026
Start date
May 2, 2023
Primary completion
Jun 26, 2023
Completion
Jun 30, 2023
Last update
Feb 6, 2026

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 Feb 2026. You cannot join it, but the record below documents what was studied.

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