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Clinical Trials/NCT07518511
NCT07518511
Completed
Not Applicable

Sensory-Enhanced Asynchronous Tele-Rehabilitation Model for Improving Function in Children With Cerebral Palsy: A Randomized Controlled Trial

Cairo University1 site in 1 country40 target enrollmentStarted: January 1, 2026Last updated:

Overview

Phase
Not Applicable
Status
Completed
Enrollment
40
Locations
1
Primary Endpoint
Nine-Hole Peg Test

Overview

Brief Summary

PURPOSE: This study evaluated the effectiveness of a Sensory-Enhanced Home-based Intensive Program (SE-HIP), delivered via asynchronous video guidance, compared to a Standard Home Program (SHP) on improving upper limb function in children with cerebral palsy (CP).

BACKGROUND: Children with cerebral palsy (CP) often have upper limb (UL) impairments that limit daily life and participation. Intensive, repetitive therapy is crucial, but traditional delivery has limitations. Home-based programs supported by tele-rehabilitation offer increased dosage and accessibility. Asynchronous models delivered via video guidance are flexible but are less studied for intensive upper limb therapy. Sensory processing deficits are common in cerebral palsy; integrating sensory enhancement may augment motor learning. Evidence combining sensory-enhanced intensive upper limb programs delivered asynchronously is lacking.

HYPOTHESES: The investigators hypothesized that children receiving the Sensory-Enhanced Home-based Intensive Program (SE-HIP) would demonstrate significantly greater improvements in primary upper limb functional outcomes, measured by the Box and Block Test (BBT) and the Nine-Hole Peg Test (NHPT), compared to those receiving the Standard Home Program (SHP).

RESEARCH QUESTION: Does a sensory-enhanced, asynchronous video-guided home program lead to significantly greater improvements in upper limb function (manual dexterity measured by the Box and Block Test (BBT) and the Nine-Hole Peg Test (NHPT)) compared to a standard video-guided home program in children with cerebral palsy (CP)?

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Participant)

Eligibility Criteria

Ages
5 Years to 10 Years (Child)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Mild spasticity (MAS 1 or 1+), independent ambulation (AFOs permitted), and the ability to follow simple instructions

Exclusion Criteria

  • Significant fixed deformities, cognitive or sensory impairments hindering participation, uncontrolled epilepsy, or recent interventions like botulinum toxin or orthopedic surgery

Arms & Interventions

Sensory-Enhanced Home-based Intensive Program (SE-HIP)

Experimental

Children receive videos that include sensory preparation and intensive motor practice as part of the Sensory-Enhanced Home-based Intensive Program (SE-HIP).

Intervention: Sensory-Enhanced Home-based Intensive Program (SE-HIP) (Other)

Standard Home Program (SHP)

Active Comparator

Children receive videos that cover standard activities as part of the Standard Home Program (SHP).

Intervention: Standard Home Program (SHP) (Other)

Outcomes

Primary Outcomes

Nine-Hole Peg Test

Time Frame: Baseline and after 6 weeks of training

Assesses fine manual dexterity (finger dexterity). The patient places and removes nine pegs into a board as quickly as possible.

Box and Block Test

Time Frame: Baseline and after 6 weeks of training

Assesses gross manual dexterity. The patient moves small wooden blocks across a partition in 60 seconds

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Tamer Mohamed El-Saeed

Associate Professor

Cairo University

Study Sites (1)

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