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

Cairo University (CU)

Status: Active, not recruiting

Conditions: Genu Recurvatum

Treatments: Procedure: Rebound Therapy; Procedure: Traditional physical therapy program; Procedure: Universal exercise unit

Study type: Interventional

Funder types: Other

Identifiers

NCT07008521

012005355

Details and patient eligibility

About

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

Full description

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.

Enrollment: 60 estimated patients

Sex: All

Ages: 5 to 7 years old

Volunteers: No Healthy Volunteers

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.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

---

60 participants in 3 patient groups

control group

Active Comparator group

Description:

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

Treatment:

Procedure: Traditional physical therapy program

study group A

Experimental group

Description:

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

Treatment:

Procedure: Universal exercise unit

Study group B

Experimental group

Description:

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

Treatment:

Procedure: Rebound Therapy