Effectiveness of Dance Therapy for Students With Mild Autism Spectrum Disorder in China

August 29, 2026 updated by: Samsilah Binti Roslan, Universiti Putra Malaysia

Effectiveness of Dance Therapy for Social Play, Emotional Regulation, Group and Communication Skills of Students With Mild Autism in China: A Cluster Randomized Controlled Trial

This study aims to evaluate the effectiveness of Dance Movement Therapy (DMT) in improving social play, emotional regulation, group skills, and communication skills among students with mild autism in China. The study will use a cluster randomized controlled trial with a pretest-posttest design. A total of 96 students aged 8-13 years will be recruited from special education schools in Linfen, Shanxi Province, China. Existing intact classes will serve as clusters and will be randomly assigned to either the DMT group or the Regular Art Class (RAC) control group. Both groups will participate in 12 weeks of intervention, conducted twice weekly, with each session lasting 45 minutes during regular art class time. Outcomes will be assessed before and after the intervention to evaluate and compare changes between the two groups.

Study Overview

Study Type

Interventional

Enrollment (Estimated)

96

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Shanxi
      • Linfen, Shanxi, China, 041000
        • Linfen Changxiang Children's Education Center
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  1. Aged between 8 and 13 years.
  2. Have a pre-existing clinical diagnosis of mild Autism Spectrum Disorder (ASD), as documented in school or medical records.
  3. Have no other serious physical health issues, such as severe chronic diseases, major surgical history, or health problems that affect quality of life.
  4. Have no prior experience with dance therapy.
  5. Written informed consent is provided by the participant's parent or legal guardian.

Exclusion Criteria:

  1. Children with serious physical health conditions that may affect their ability to participate in the study.
  2. Children with prior experience in dance therapy.
  3. Children whose parent or legal guardian does not provide written informed consent.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Dance Movement Therapy (DMT) Group
Participants in this group will receive a 12-week Dance Movement Therapy (DMT) intervention, conducted twice weekly, with each session lasting 45 minutes during regular art class time.

The Dance Movement Therapy (DMT) intervention will be delivered over 12 weeks, with two 45-minute sessions per week. Each session will include a warm-up phase, a core activity phase, and a closing phase, with additional time used flexibly for transitions and emotional adjustment. The intervention will use structured and creative movement activities, including mirror exercises, rhythm synchronization, spatial exploration, improvisational movement, symbolic movement, role-playing, cooperative activities, and relaxation exercises.

The intervention will progress through three phases. Weeks 1-4 will focus on bodily awareness and spatial perception; Weeks 5-8 will focus on emotional expression, emotional regulation, social interaction, and cooperation; and Weeks 9-12 will focus on confidence, creativity, complex emotional understanding, and integration of previously developed skills. Activities will be adjusted to participants' responses and individual needs.

Active Comparator: Regular Art Class (RAC) Group
Participants in this group will participate in Regular Art Class (RAC) activities for 12 weeks, conducted twice weekly, with each session lasting 45 minutes during regular art class time.

The Regular Art Class (RAC) intervention will be delivered over 12 weeks, with two 45-minute sessions per week, following the school's conventional art curriculum. The program will include one Music and Rhythmic Movement session and one Art and Craft session per week. Sessions will consist of structured, teacher-guided activities and will typically include warm-up activities, theme-based learning, creative practice, and summary sharing, with additional time reserved for transitions and students' emotional needs.

Music and Rhythmic Movement sessions will include singing, rhythm practice, simple body movements, group games, and cooperative activities. Art and Craft sessions will primarily include handicraft and collage activities during the first eight weeks, followed by painting activities from Week 9 onward. The activities will focus on creative expression, basic artistic skills, classroom participation, rhythmic abilities, fine motor skills, imagination, observation, color expression

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Social Play Assessed by the Penn Interactive Peer Play Scale (PIPPS)
Time Frame: Baseline and immediately after the 12-week intervention
Social play will be assessed using the Penn Interactive Peer Play Scale (PIPPS), a 32-item teacher-rated measure of peer play behaviors. The PIPPS assesses three dimensions: Play Interaction, Play Disruption, and Play Disconnection. Items are rated on a four-point Likert scale (never, seldom, often, and always). Higher Play Interaction scores indicate more positive peer play interactions, whereas higher Play Disruption and Play Disconnection scores indicate greater disruptive behavior and disengagement from peer play, respectively. Scores will be calculated according to the established PIPPS scoring procedures.
Baseline and immediately after the 12-week intervention
Change in Emotional Regulation Assessed by the Chinese Version of the Emotion Regulation Checklist (ERC-C)
Time Frame: Baseline and immediately after the 12-week intervention
Emotional regulation will be assessed using the Chinese Version of the Emotion Regulation Checklist (ERC-C), a 24-item rating scale completed by a parent, teacher, or other adult familiar with the child. The ERC-C assesses two dimensions: Emotion Regulation and Lability/Negativity. Items are rated on a 7-point Likert scale from 1 (completely untrue) to 7 (completely true). Emotion Regulation reflects adaptive emotional regulation, whereas Lability/Negativity reflects emotional reactivity and dysregulation. Scores will be calculated according to the established scoring procedures.
Baseline and immediately after the 12-week intervention
Change in Group Skills Assessed by the Social Skills Subscale of the Chinese Version of the School Social Behavior Scales (SSBS-C)
Time Frame: Baseline and immediately after the 12-week intervention
Group skills will be assessed using the 32-item Social Skills subscale of the Chinese Version of the School Social Behavior Scales (SSBS-C), completed by teachers or other school staff familiar with the child. The subscale assesses three dimensions: Interpersonal Skills, Self-Management Skills, and Academic Skills. Items are rated on a 5-point scale from 1 (never occurs) to 5 (always occurs). Higher scores indicate stronger social skills, including interpersonal interaction, self-management, and skills relevant to effective participation and functioning in group settings.
Baseline and immediately after the 12-week intervention
Change in Communication Skills Assessed by the Chinese Version of the Communication Matrix (CM-C)
Time Frame: Baseline and immediately after the 12-week intervention
Communication skills will be assessed using the Chinese Version of the Communication Matrix (CM-C), a functional communication assessment for individuals with limited verbal or spoken communication. The assessment evaluates communication across seven developmental levels, ranging from pre-intentional behavior to abstract symbolic communication, and includes multiple forms of communication such as gestures, facial expressions, vocalizations, pictures, and other augmentative and alternative communication methods. For quantifying change, individual communication behaviors are scored as 0 (not used), 1 (emerging), or 2 (mastered). The total score ranges from 0 to 160, with higher scores indicating more developed functional communication skills.
Baseline and immediately after the 12-week intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

September 20, 2026

Primary Completion (Estimated)

January 20, 2027

Study Completion (Estimated)

January 20, 2027

Study Registration Dates

First Submitted

August 29, 2026

First Submitted That Met QC Criteria

August 29, 2026

First Posted (Actual)

September 2, 2026

Study Record Updates

Last Update Posted (Actual)

September 2, 2026

Last Update Submitted That Met QC Criteria

August 29, 2026

Last Verified

August 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • UPM-EDU-DMT-2026-001
  • JKEUPM-2025-725 (Other Identifier: Universiti Putra Malaysia Ethics Committee for Research Involving Human Subjects (JKEUPM))

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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