UNIVERSAL EXERCISE UNIT and REBOUND THERAPY ON GENU RECURVATUM Cerebral Palsy Childeren

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

ACTIVE_NOT_RECRUITING

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-03-01

Study Completion Date

2025-10-01

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

to investigate and compare between effectiveness of Universal Exercise Unit and Rebound Therapy on genu recurvatum, muscle strength, balance, functional mobility and quality of life in spastic cerebral palsy children

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Cross-Training and Locomotor Abilities in Cerebral Palsy

NCT06750081

Cerebral Palsy (CP) Spastic Hemiparesis

COMPLETED NA

Universal Exercise Unit Versus Functional Electrical Stimulation On Genu Recurvatum In Diplegic Cerebral Palsy

NCT06332729

Cerebral Palsy

COMPLETED NA

Role of Rebound Therapy in the Rehabilitation of Children With Spastic Cerebral Palsy

NCT04712708

Cerebral Palsy

UNKNOWN NA

Effect of Core Stability Excercises Program on Reaching in Children With Cerebral Palsy

NCT05316090

Cerebral Palsy

COMPLETED NA

Effectiveness of Universal Exercise Unit Exercise on Upper Limb Strength Using Biodex Isokinetic

NCT07233031

Cerebral Palsy Spastic Hemiplegic

COMPLETED NA

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Children will be equally assigned into three groups using simple randomization, control group, study group (A) and study group (B). Each group will consist of 20 children with spastic CP to overcome any drop out may occur.

Control group: Children in this group will receive a traditional physical therapy program.

Study group (A): Children in this group will receive a traditional physical therapy program in addition to universal exercise unit program.

Study group (B): Children in this group will receive the same traditional physical therapy program in addition to rebound therapy.

Evaluation will be carried out for each child individually before and after 3 months of treatment.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Genu Recurvatum

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Participants will be assigned randomly into three groups of equal number (control group, study group A and study group B ) the randomization will be performed by simple randomization. Assessors will be blinded to the groups of the subjects.

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

control group

Control group: Children in this group will receive a traditional physical therapy program.

Group Type ACTIVE_COMPARATOR

Traditional physical therapy program

Intervention Type PROCEDURE

traditional physical therapy program for contrl group

study group A

Study group (A): Children in this group will receive a traditional physical therapy program in addition to universal exercise unit program.

Group Type EXPERIMENTAL

Universal exercise unit

Intervention Type PROCEDURE

universal exercise unit (UEU) for study groip (A)

Study group B

Study group (B): Children in this group will receive the same traditional physical therapy program in addition to rebound therapy

Group Type EXPERIMENTAL

Rebound Therapy

Intervention Type PROCEDURE

rebound therpay for study group (B)

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Universal exercise unit

universal exercise unit (UEU) for study groip (A)

Intervention Type PROCEDURE

Rebound Therapy

rebound therpay for study group (B)

Intervention Type PROCEDURE

Traditional physical therapy program

traditional physical therapy program for contrl group

Intervention Type PROCEDURE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* -Children with spastic CP both hemiplegic and diplegic.
* Their ages will be ranged from 5-7 years old.
* They will have mild spasticity (grade 1 and 1+) according to Modified Ashworth scale .
* They will be in level I and II according to gross motor function classification system (GMFCS) .
* They will be able to understand orders given to them.

Exclusion Criteria

* Subjects will be excluded if they have the following:

1. Visual or hearing impairment.
2. Severe limb deformities as structural genurecurvatum.
3. Surgical interference in the lower limbs for the last 6 months.
4. Botulinum toxin injection of the spastic lower limb muscles during the last six months.

Minimum Eligible Age

5 Years

Maximum Eligible Age

7 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No