Animal Fun Program and Kinesthetic Development in Down Syndrome

May 5, 2026 updated by: Riphah International University

Effects of Animal Fun Program on Kinesthesia in Children With Down Syndrome

The purpose of the study is that Animal-fun activities capture children's attention, making them a powerful tool for enhancing kinesthetic awareness and gross motor skills. Although play-based programs like Animal Fun boost motor development, no research has yet examined if adding animal interaction can specifically improve proprioception in children with Down syndrome. There is no difference in the effects of animal fun program on kinesthesia in children with Down syndrome.There is a difference in the effects of animal fun program on kinesthesia in Children with Down syndrome.

Study Overview

Status

Recruiting

Intervention / Treatment

Detailed Description

Down syndrome (DS), resulting from a full or partial extra copy of chromosome 21 in approximately 1 in 650-1,000 live births, represents the most frequent genetic origin of intellectual disability and is often accompanied by delayed attainment of motor developmental milestones. Insufficient motor coordination and proprioceptive awareness can significantly limit participation in physical activities. Proprioceptive input mediated by muscle spindles, joint and skin receptors, and Golgi tendon organs underlies kinesthesia, our sensory perception of movement and spatial orientation. The Animal Fun program, a structured, inclusive early intervention originally designed for typically developing children, has demonstrated effectiveness in improving gross and fine motor skills, balance, manual dexterity, and socio-emotional development.The study design will be Quasi Experimental Study. This study will recruit 26 children of Down Syndrome to evaluate a modified Animal Fun program on Kinesthesia in children with down syndrome. Animal fun program will be provided for 8 weeks and in one week four sessions will be conducted. The study will be completed in 10 months after the approval of synopsis. Data will be collected from step up rehabilitation center Lahore. Participants fulfilling the eligibility criteria will be asked to assign the consent form before entering into study. Kinesthesia effect will be assessed by joint position sense test. A goniometer measures joint angles and accuracy is calculated by comparing target and reproduced angles. The synopsis will presented to the Research Ethical Committee of Riphah International University, Lahore for ethical approval to conduct this study. Data will be analyzed through SPSS version 26.0.

Study Type

Interventional

Enrollment (Estimated)

26

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 Contact Backup

Study Locations

    • Punjab Province
      • Lahore, Punjab Province, Pakistan, 54000

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:

  • Children aged 6 to 9 years
  • Diagnosed with Down's Syndrome
  • Both male and female will be included
  • Parental/Guardian Consent or Written informed consent must be obtained from parents or legal guardians.
  • Regular Attendance or Availability and willingness to participate in all scheduled sessions of the Animal Fun Program.

Exclusion Criteria:

  • Presence of Neurological and Musculoskeletal Disorders
  • Visual or Hearing Impairments
  • Behavioral or Psychiatric Conditions
  • Recent Orthopedic or Neurosurgical Interventions
  • Irregular Attendance Risk

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: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Animal fun program
The experimental group will receive animal fun program, the program includes 30 minutes each day for 4 days/ week, usually with an outdoor session of 15 minutes and an indoor session of 15 minutes per day.

The Animal Fun program, consists of the following modules:

Module 1: Body Management (Static balance, Dynamic balance, climbing) Module 2: Locomotion (Walking, Jumping, Hopping, Skipping) Module 3: Object Control (Throwing, Catching, Kicking) Module 4: Body Sequencing (Trunk, Limbs) Module 5: Body and Kinesthetic Management: Trunk and Upper Limb (Eye hand coordination, Visual kinesthetic) Module 6: Fine Motor Planning Module 7: Tool Control (Pre-scissor/scissor skills, Paint brush use, Drawing/pre-writing skills).

Module 8: Hand Skills (Individual finger strength, Grip strength, Pincer grip) Module 9: Social/Emotional Development (Laughter, Identifying and labelling feelings, Breathing, Relaxation).

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Joint position sense test
Time Frame: Baseline, 8 weeks
Joint Position Sense (JPS) testing was conducted using a standardized protocol and a consistent measurement tool, specifically a goniometer, to assess the accuracy of joint angle reproduction. The difference between the reference angle and the reproduced angle was calculated to determine the Joint position sense test (JPS) error, with greater differences indicating larger deficits. A score of zero was assigned if the participant exactly reproduced the reference angle. Although directionality (over- or underestimation) was noted, only the absolute values of angle differences were used for final analysis.
Baseline, 8 weeks

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Sadia Khan, MS-PT, Riphah International University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the 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 (Actual)

April 1, 2026

Primary Completion (Estimated)

July 1, 2026

Study Completion (Estimated)

July 1, 2026

Study Registration Dates

First Submitted

May 5, 2026

First Submitted That Met QC Criteria

May 5, 2026

First Posted (Actual)

May 12, 2026

Study Record Updates

Last Update Posted (Actual)

May 12, 2026

Last Update Submitted That Met QC Criteria

May 5, 2026

Last Verified

May 1, 2026

More Information

Terms related to this study

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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