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Clinical Trials/NCT07757035
NCT07757035CompletedNot Applicable

Effects of Low Frequency Whole Body Vibrations on Motor Skills and Sensory Integration in Children With Autism

Riphah International University1 site in 1 country36 target enrollmentStarted: April 15, 2026Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
36
Locations
1
Primary Endpoint
Test for Gross motor function-2 (TGMD-2)

Study Overview

Brief Summary

This randomized controlled trial aims to evaluate the efficacy of low-frequency Whole Body Vibration therapy on motor skills and sensory integration in children aged 5-9 years diagnosed with mild to moderate ASD.

Detailed Description

Autism Spectrum Disorder (ASD) is a complex neurodevelopmental condition characterized by deficits in social communication and restrictive, repetitive behaviors. While core symptoms often receive priority in diagnosis and intervention, motor coordination difficulties and sensory integration challenges-present in a significant proportion of autistic children- remain underexplored. Research shows that up to 83% of children with ASD struggle with age-appropriate motor skills, and sensory processing abnormalities further hinder their participation in daily routines. Traditional therapies, although beneficial, often fail to address these interconnected domains comprehensively. Whole-body vibration (WBV) therapy, a non-invasive physical intervention that stimulates neuromuscular function through low frequency vibrations, has shown promise in improving motor control, coordination, and even behavioral outcomes in various clinical populations, including children with cerebral palsy and Down syndrome. However, its application in pediatric ASD, particularly for sensory and motor integration, remains limited in empirical evidence. This randomized controlled trial aims to evaluate the efficacy of low-frequency Whole Body Vibration therapy on motor skills and sensory integration in children aged 3-10 years diagnosed with mild to moderate ASD. The study will be conducted over 10 months at two pediatric rehabilitation centers in Pakistan and will involve 36 participants divided into intervention and control groups. The intervention group will receive low-frequency Whole Body Vibration sessions combined with routine physiotherapy, while the control group will engage in routine physical activity. Motor skills will be assessed using the Test of Gross Motor Development-2 (TGMD-2), and sensory processing will be evaluated with the Short Sensory Profile. The vibration protocol includes 3-4 rounds of 30-second sessions with rest intervals, using a platform set at 28 Hz and 0.97 mm amplitude. Data will be analyzed using SPSS 27.0.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Investigator)

Eligibility Criteria

Ages
5 Years to 9 Years (Child)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Children aged 5-9 years
  • •Clinically diagnosed with mild to moderate Autism Spectrum Disorder according to the childhood autism rating scale (CARS)
  • •Able to stand or sit with support on a WBV platform
  • •Children able to follow simple verbal commands
  • •Children with no visual or auditory defects
  • •Parental/legal guardian consent obtained
  • •Attending regular therapy sessions at the study site

Exclusion Criteria

  • •Children with uncontrolled epilepsy and cerebral palsy
  • •Severe musculoskeletal or orthopedic impairments
  • •Presence of implanted medical devices (e.g., pacemaker)
  • •Any recent surgery (<6 months)
  • •Children currently undergoing another experimental therapy

Arms & Interventions

Whole body vibration group

Experimental

The participants in this group will receive the low-frequency whole-body vibration therapy along with routine physical activity For whole body vibration: Frequency: 5 Hz Amplitude: 2.5 mm Each session will include 5 vibration periods, each lasting 30 seconds. A 1min rest interval will be provided between each vibration period. Upon completion of each session, the participant will be taken immediately to the observation room. A 5-minute post-session observation period will be conducted to monitor behavioral or physiological response Each participant will undergo between 10 and 40 individual sessions, depending on their tolerance and the requirement for data stability.

Intervention: whole body vibration (Other)

Routine physical therapy group

Other

10 min session per day. 5 session per week. Walk/Jog session at moderate intensity during the early hours of the day.

Intervention: Routine physical therapy (Other)

Outcomes

Primary Outcomes

Test for Gross motor function-2 (TGMD-2)

Time Frame: 8 weeks

TGMD-2 includes motor exercises that are focused on improving motor performance levels. The first part of the locomotor subtest exercises includes a run, gallop, hop, leap, horizontal jump and slide. The second part of the object control subtest exercises includes striking a stationary ball, stationary dribble, catch, kick, overhand throw and underhand roll. During the test, each child had to perform each exercise twice. A total of 3- 5 performance criteria were used for the evaluation. If the given criterion was not performed correctly, it was marked 0. Conversely, if the given criterion was performed correctly, it was marked 1. The internal consistency of the TGMD-2 was found to be high (alpha = 0.71-0.72) and the interrater, interrater, and test-retest reliability acceptable (ICCs ranging from 0.82 to 0.95)

Sensory profile questionnaire

Time Frame: 8 weeks

The Sensory Profile Questionnaire is a 125-item tool designed for use with children aged 3 to 10 years. It employs a 5-point Likert scale and covers eight sensory categories: Auditory, Visual, Taste/Smell, Movement, Body Position, Touch, Activity Level, and Emotional/Social. Scores are calculated individually for three main sections-Sensory Processing, Modulation, and Behavioral and Emotional Responses-as well as for each specific factor. A lower total score on the SPCQ indicates greater sensory processing difficulties.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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