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Investigation of Psychosocial Effects of Dance/Movement Therapy in Children With Specific Learning Disorders

2026年9月21日 更新者:Arif Gökcen、Lokman Hekim University

Investigation of Psychosocial Effects of Dance/Movement Therapy in Children With Specific Learning Disorders: a Randomized Controlled Study With 6 Months Follow-up

This randomized controlled trial examined whether dance/movement therapy (DMT) can improve emotional and social well-being in children with specific learning disorder (SLD). Children aged 8-12 years with SLD who were receiving special education services in Muğla, Türkiye, were randomly assigned to either an 8-week group DMT program in addition to their usual special education services or to usual special education services alone. Anxiety and depressive symptoms, self-esteem, and social skills were assessed before the intervention, after the intervention, and at a 6-month follow-up.

研究概览

地位

完全的

详细说明

Specific learning disorder is associated with emotional and social difficulties beyond academic problems. In this two-arm, parallel-group randomized controlled trial, eligible children were randomly allocated (1:1) to a DMT group or a control group using a computer-generated randomization sequence prepared by an independent statistician. The DMT program consisted of 16 group sessions (45 minutes each, twice weekly, over 8 weeks) delivered in small groups of 6-8 children. Each session followed a standardized five-phase structure (warm-up, improvisation, skill development, integration, and closure) based on the principles of the GAMZE (Gaining Accurate Mobility with Zealous Effort) style and the BrainDance model. Both groups continued to receive their usual special education services. Parents completed the Revised Child Anxiety and Depression Scale-Parent Version and the Social Skills Evaluation Scale, and children completed the Coopersmith Self-Esteem Inventory-School Form. Data were analyzed using linear mixed-effects models.

研究类型

介入性

注册 (实际的)

46

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

8年 至 12年 (孩子)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Age 8-12 years
  • Diagnosis of specific learning disorder according to DSM-5 within the preceding 12 months, verified by a valid Child with Special Needs Report (ÇÖZGER)
  • Enrollment in a primary school affiliated with the Turkish Ministry of National Education, with at least one semester of formal schooling completed
  • Current enrollment in a special education and rehabilitation center

Exclusion Criteria:

  • Co-occurring physical, neurological, psychiatric, or other neurodevelopmental condition that could interfere with participation or substantially affect study outcomes
  • Receiving or initiating any treatment targeting neurodevelopmental, emotional, behavioral, or psychosocial functioning during the study period
  • Regular participation in organized sports or other structured physical activities outside routine school and recreational activities

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Dance/Movement Therapy

Children received 16 sessions of group dance/movement therapy (45 minutes, twice weekly, for 8 weeks) in addition to their usual special education

A structured, goal-oriented group program based on the GAMZE style and the BrainDance model. Each 45-minute session included warm-up (5 min), improvisation (10 min), skill development (15 min), integration (10 min), and closure (5 min). Sessions were delivered in groups of 6-8 children by an experienced therapist trained in goal-oriented DMT.

其他名称:
  • DMT
无干预:Control

Children continued to receive their usual special education services without

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Change in Revised Child Anxiety and Depression Scale-Parent Version (RCADS-P) Total Score
大体时间:Baseline, week 8 (post-intervention), and month 6 (follow-up)

Parent-reported 47-item scale assessing anxiety and depressive symptoms (total score range 0-141); higher scores indicate greater symptom severity.

Baseline, week 8 (post-intervention), and month 6 (follow-up)
Change in Coopersmith Self-Esteem Inventory-School Form (CSEI) Total Score
大体时间:Baseline, week 8 (post-intervention), and month 6 (follow-up)

Child-reported inventory assessing general, social, home/family, and academic self-esteem; higher scores indicate higher self-esteem.

Baseline, week 8 (post-intervention), and month 6 (follow-up)
Change in Social Skills Evaluation Scale (SSES) Total Score
大体时间:Baseline, week 8 (post-intervention), and month 6 (follow-up)

Parent-reported 69-item scale assessing social skills across 12 domains (total score range 69-345); higher scores indicate better social skills.

Baseline, week 8 (post-intervention), and month 6 (follow-up)

次要结果测量

结果测量
措施说明
大体时间
Change in RCADS-P Anxiety and Depression Subscale Scores
大体时间:Baseline, week 8 (post-intervention), and month 6 (follow-up)

Anxiety subscale (range 0-111) and depression subscale (range 0-30); higher scores indicate greater symptom severity.

Baseline, week 8 (post-intervention), and month 6 (follow-up)
Change in CSEI Subscale Scores
大体时间:Baseline, week 8 (post-intervention), and month 6 (follow-up)

General, social, home/family, and academic self-esteem subscales; higher scores indicate higher self-esteem.

Baseline, week 8 (post-intervention), and month 6 (follow-up)
Change in SSES Subscale Scores
大体时间:Baseline, week 8 (post-intervention), and month 6 (follow-up)

Twelve social skills domains; higher scores indicate better social skills.

Baseline, week 8 (post-intervention), and month 6 (follow-up)

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2024年6月15日

初级完成 (实际的)

2025年3月11日

研究完成 (实际的)

2025年4月15日

研究注册日期

首次提交

2026年9月21日

首先提交符合 QC 标准的

2026年9月21日

首次发布 (实际的)

2026年9月28日

研究记录更新

最后更新发布 (实际的)

2026年9月28日

上次提交的符合 QC 标准的更新

2026年9月21日

最后验证

2026年9月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

是的

IPD 计划说明

De-identified individual participant data underlying the published results will be available from the corresponding author upon reasonable request after publication.

IPD 共享支持信息类型

  • 研究方案
  • 国际碳纤维联合会
  • 企业社会责任

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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