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Cerebral Palsy Spastic DiplegiaNCT07731074

Oculomotor Training in Spastic Diplegia: Effects on Postural Stability and Motor Proficiency

A study testing Oculomotor Training and Conventional Physiotherapy in people with Cerebral Palsy Spastic Diplegia, run by Cairo University at 1 site in Egypt.

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record

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Trial summary

This randomized clinical trial investigates the effect of oculomotor training on postural stability and motor proficiency in children with spastic diplegia. Participants will undergo structured oculomotor exercises designed to enhance visual-motor integration and balance control. Read more about this study

Who is it for?
Ages 6 to 10 years
Conditions the study is for
Cerebral Palsy Spastic Diplegia
What is being tested?
Oculomotor Training and Conventional Physiotherapy
Could I receive a placebo?
No, everyone receives an active treatment
How many people
34 participants
Where
1 siteEgypt
Study dates
1 Jun 2026to 30 Nov 2026
Phase
Interventional

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 6 to 10 years
  • All sexes
  • No healthy volunteers
  • Child

Who may be able to join

  • Their ages will range from 6 to 10 years old. -The degree of spasticity will range from grade 1and1+ according to the Modified Ashworth Scale (MAS)-
  • They will be at level I or II according to gross motor classification system (GMFCS).
  • They will have mild and moderate visual impairment without (CVI) according to visual assessment scale.
  • They will be able to follow verbal command or instructions.

Who cannot join

  • Uncontrolled seizures.
  • Severe vestibular dysfunction.
  • Recent orthopedic surgery (within 6 months).
  • Severe visual impairment

Trial locations and contacts

1 site in 1 country.

Egypt1 site
  • faculty of physical therapy Cairo university

    Cairo

Other trials in Egypt

About this study

Official title: EFFECT OF OCULOMOTOR TRAINING ON POSTURAL STABILITY AND MOTOR PROFICIENCY IN CHILDREN WITH SPASTIC DIPLEGIA

This randomized clinical trial investigates the effect of oculomotor training on postural stability and motor proficiency in children with spastic diplegia. Participants will undergo structured oculomotor exercises designed to enhance visual-motor integration and balance control. Outcomes will be assessed using standardized measures of postural stability and motor proficiency before and after intervention. The study aims to determine whether targeted oculomotor training can improve functional motor performance and balance in this pediatric population.

By evaluating the effect of structured oculomotor training on postural stability and motor proficiency in children with spastic diplegia, the study seeks to establish whether visual-motor interventions can serve as effective adjuncts to conventional therapy. The rationale is grounded in neuroplasticity: repeated oculomotor exercises may strengthen neural pathways linking visual input to motor output, thereby improving balance and functional performance.

Being tested
Oculomotor Training, Conventional Physiotherapy
Keywords
Oculomotor training, Postural stability, Spastic diplegia ,Cerebral palsy, Motor proficiency, Pediatric rehabilitation
Medical subject headings
Cerebral Palsy

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Oculomotor TrainingBehavioural

    Exercises include saccadic eye movements, smooth pursuit, fixation, and visual scanning tasks.

  • Conventional PhysiotherapyBehavioural

    physiotherapy focusing on stretching, strengthening, and balance training.

Study groups in NCT07731074
Study groupRoleWhat they receive
Oculomotor Training + Conventional PhysiotherapyExperimentalIntervention: Participants receive a structured oculomotor training program in addition to Conventional Physiotherapy. Details: Exercises include saccadic eye movements, smooth pursuit, fixation, and visual scanning tasks. Sessions: 45 minutes of Conventional Physiotherapy and 45 minutes of Oculomotor Training , 3 times per week, for 12 weeks. Purpose: To evaluate whether oculomotor training enhances postural stability and motor proficiency beyond conventional therapy.
Receives: Behavioral: Oculomotor Training; Behavioral: Conventional Physiotherapy
Conventional Physiotherapy OnlyActive comparatorParticipants receive standard physiotherapy focusing on stretching, strengthening, and balance training. Details: Sessions matched in duration and frequency to the experimental arm (45 minutes, 3 times per week, for 12 weeks). Purpose: Serves as a comparator to determine the added value of oculomotor training.
Receives: Behavioral: Conventional Physiotherapy

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Postural Stability Index

    Overall Stability Index (OSI) from the Biodex Balance System.

    Measured: 12 weeks

Secondary outcomes (1)
  1. Motor Proficiency

    Measure: Bruininks-Oseretsky Test of Motor Proficiency, Second Edition (BOT-2).

    Measured: 12 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted28 Jul 2026
  2. Study start1 Jun 2026
  3. Primary completion15 Oct 2026 (estimated)
  4. Study completion30 Nov 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
34 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07731074
Sponsor's protocol ID
P.T.REC/012/006212
Status last verified
Jul 2026
First submitted
23 Jul 2026
Last updated
28 Jul 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: study report about our work and results will be published

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