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Comparison of Sensory Integration Therapy and Conventional Physical Therapy on Gross Motor Function in Children With Athetoid Cerebral Palsy: A Randomized Controlled Trial

NCT07611565 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 26

Last updated 2026-05-28

No results posted yet for this study

Summary

This is an RCT aiming to explore the comparison of Sensory Integration Therapy and Conventional Physical Therapy on Gross Motor Function in Children with Athetoid Cerebral Palsy

Conditions

  • Athetoid CP
  • Cerebral Palsy (CP)

Interventions

OTHER

Sensory Integration Therapy and Conventional Physical Therapy

Three sessions per week for 6 weeks, Moderate Intensity, 45 minutes per session Vestibular Control (5 minutes): * Slow linear swinging * Therapy-ball side shifts * Graded rocking Proprioceptive Input (5 minutes): * Joint compression * Weighted pushing/pulling * Thera-band control tasks Midline \& Postural Stability (5 minutes): * Controlled reaching * Supported sitting on wedge/bolster * Trunk stabilization task Tactile-Motor Integration (5 minutes): Vestibular Control (5 minutes): * Slow linear swinging * Therapy-ball side shifts * Graded rocking Proprioceptive Input (5 minutes): * Joint compression * Weighted pushing/pulling * Thera-band control tasks Midline \& Postural Stability (5 minutes): * Controlled reaching * Supported sitting on wedge/bolster * Trunk stabilization task Tactile-Motor Integration (5 minutes):

OTHER

Conventional Physical Therapy

Three sessions per week for 6 weeks, Moderate Intensity, 45 minutes per session 1. Stretching (10 min): • Hamstrings, hip flexors, heel cord, trunk 2. Strengthening (15 min): * Core stabilization (bridging, supported plank), * LL strengthening (mini-squats, step training) 3. Balance Training (10 min): Sitting on therapy ball with support, standing balance with controlled BOS 4. Gait \& Functional Mobility (10 min): Parallel bar gait Controlled stepping Sit-stand \& kneeling Standing transitions

Sponsors & Collaborators

  • Ibadat International University, Islamabad

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
6 Years
Max Age
12 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-03-10
Primary Completion
2026-09-15
Completion
2026-09-20

Countries

  • Pakistan

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07611565 on ClinicalTrials.gov