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Effects of Kinetic Sand on Functional Reach and Eye-Hand Coordination in Children With Autism

2026年5月5日 更新者:Riphah International University
A quasi-experimental pre-post study will be conducted at pediatric therapy clinics and special education centers, involving 17 children aged 6-12 years diagnosed with mild to moderate ASD, selected through convenient sampling. The intervention will consist of kinetic sand play for 30 minutes, three times per week, over six weeks, including activities such as molding objects, searching for hidden items, and free play to enhance creativity, grip strength, and coordination. Eye-hand coordination and functional reach will be assessed using the Purdue Pegboard Test (PPT) and the Functional Reach Test. Data will be analyzed using SPSS Version 26 with paired t-tests or appropriate non-parametric methods. Ethical approval will be obtained from the Research Ethical Committee of Riphah International University, Lahore.

研究概览

地位

招聘中

详细说明

Children with autism often experience deficits in fine motor skills, sensory processing, and motor coordination, which can significantly impede their ability to perform functional tasks such as reaching and manipulating objects. Kinetic sand, with its unique moldable and tactile properties, offers a multisensory experience that encourages repetitive hand movements, proprioceptive input, and tactile engagement.

These characteristics make it an ideal medium to potentially improve functional reach and eye-hand coordination. The intervention is designed to provide calming sensory input that may reduce tactile defensiveness and anxiety, thereby facilitating greater focus and motor control. The purpose of this study is to evaluate the therapeutic efficacy of kinetic sand as a sensory-motor intervention for children with Autism Spectrum Disorder (ASD). A quasi-experimental study that follows a single group before and after ten months will occur at various pediatric therapy clinics and special education centers. Seventeen children between 6 and 12 years old, diagnosed with mild to moderate ASD, will be invited using non-probability convenient sampling, after allowing for the effect of potential dropouts. The intervention will last six weeks and consists of playing with kinetic sand for 30 minutes, three times every week. Activities will require molding objects, looking for hidden items, and simply playing freely to help children get creative, improve their grips, and learn coordination. The Purdue Pegboard Test (PPT) and Functional Reach test will be used to study changes in hand-eye coordination and in reaching tasks. Scores will be analyzed by SPSS Version 26, either with paired t- tests or with non-parametric methods based on what is suitable. The conclusions might assist therapists in applying sensory-motor therapy to children with autism in Pakistan. The synopsis will be presented to the Research Ethical Committee of Riphah International University, Lahore, for ethical approval to conduct this study.

研究类型

介入性

注册 (估计的)

17

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。

学习联系方式

研究联系人备份

学习地点

    • Punjab Province
      • Lahore、Punjab Province、巴基斯坦、5400
        • 招聘中
        • Imran Amjad
        • 接触:
        • 接触:

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

  • 孩子

接受健康志愿者

不

描述

Inclusion Criteria:

  • According to DSM-5 criteria, characterized by persistent deficits in social communication and interaction
  • Restricted, repetitive patterns of behavior or interests
  • Children demonstrating measurable impairments in functional reach and eye-hand coordination
  • Able to follow instructions

Exclusion Criteria:

  • Children with severe intellectual disability, cerebral palsy, epilepsy or other neurological conditions that significantly impair motor function
  • Children currently receiving other intensive occupational or physical therapy targeting functional reach or eye-hand coordination
  • Presence of musculoskeletal deformities, severe visual impairments, or other medical conditions independently affecting motor skills or coordination

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:其他
  • 分配:不适用
  • 介入模型:单组作业
  • 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:Kinetic sand play
After obtaining consent, the patient was introduced to a rehabilitation protocol combining traditional physiotherapy for the wrist and hand with kinetic sand therapy. The program included range of motion exercises, grip strengthening, and kinetic sand activities, performed for 40 minutes per session, 6 days per week, over 7 weeks. This comprehensive approach aimed to reduce pain and swelling while improving hand function, strength, and coordination.
After obtaining consent, the patient was introduced to a rehabilitation protocol combining traditional physiotherapy for the wrist and hand with kinetic sand therapy. The program included range of motion exercises, grip strengthening, and kinetic sand activities, performed for 40 minutes per session, 6 days per week, over 7 weeks. This comprehensive approach aimed to reduce pain and swelling while improving hand function, strength, and coordination.

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
Functional Reach
大体时间:7 weeks
To assess functional reach before and after the intervention, the Functional Reach Test will be used to evaluate improvements in balance and reaching ability. This method allows measurement of the maximum distance a child can reach forward beyond arm's length while maintaining a stable standing position. Changes in reach distance will indicate improvements in postural control, stability, and functional mobility, reflecting the effectiveness of the intervention.
7 weeks
Eye-Hand Coordination
大体时间:7 weeks
To assess eye-hand coordination before and after the intervention, the Purdue Pegboard Test will be used to evaluate improvements in fine motor skills and coordination. This method allows measurement of hand dexterity, speed, and accuracy by recording the number of pins placed within a specific time. Changes in scores will indicate improvements in coordination between visual input and hand movements, reflecting the effectiveness of the intervention.
7 weeks

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。

调查人员

  • 首席研究员:Huma Mumtaz, MS-PT、Riphah International University

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

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)

2025年10月28日

初级完成 (估计的)

2026年5月5日

研究完成 (估计的)

2026年6月15日

研究注册日期

首次提交

2026年5月5日

首先提交符合 QC 标准的

2026年5月5日

首次发布 (实际的)

2026年5月11日

研究记录更新

最后更新发布 (实际的)

2026年5月11日

上次提交的符合 QC 标准的更新

2026年5月5日

最后验证

2026年5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)?

不

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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