Functional Progressive Resistive Training and Cerebral Palsy

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age6-10
SponsorCairo University

About this trial

Functional Progressive Resistive Exercise (FPRE) is a strengthening approach that combines functional movement activities with progressively increased resistance. It involves performing task-oriented exercises, such as sit-to-stand, stair climbing, and walking-related activities, while gradually increasing the load to enhance muscle strength, endurance, and functional performance. FPRE is widely used in rehabilitation programs to improve mobility and the ability to perform activities of daily living in various populations, including children with neurological and musculoskeletal disorders.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

A diagnosis of spastic diplegic CP

Degree of spasticity ranges from 1+ and 2, according to modified Ashworth scale (MAS)

The age of the selected children will range from 6 to 10 years old.

Children are levels II and III according to GMFCS

Disqualifiers

None

Trial design

Design model

Parallel

Treatments tested in this trial

  • functional progressive resistive exercise and designed physical therapy program

    Other intervention

    specially designed physical therapy program in addition to functional progressive resistive exercises for 60 min (30 min designed P.T program and other 30 min for brain gym exercises), 3 sessions/ week for 3 successive months. 6 functional progressive resistive exercises will be selected: 1. Sit-to-Stand Exercise 2. Step-Up Exercise 3. Squats 4. Lunges 5. Stair Climbing 6. Loaded Walking

  • designed physical therapy program

    Other intervention

    conventional physical therapy program including reinforcement of the normal motor development, reflex inhibiting patterns, postural reaction, stretching, strengthening exercises, and gait training was applied to children in the control group

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: functional progressive resistive exercise and designed physical therapy programExperimental treatment 1 intervention
Group B: designed physical therapy programExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Dual-energy X-ray absorptiometry (DXA)

The most common test for bone mineral density is a Dual-energy X-ray absorptiometry (DXA) scan. It is: Painless and non-invasive Quick (usually 10-20 minutes) Low radiation exposure Most often performed on the hip and lower spine. Bone mineral density (BMD) is a measure of the amount of mineral (mainly calcium and phosphorus) present in a specific volume of bone. It reflects bone strength and is used to assess the risk of fractures and diagnose osteoporosis.

Time frame
3month
2

biodex balance system

The Biodex Balance System is a computerized device used to assess and improve static and dynamic balance, postural stability, and neuromuscular control. It consists of a movable platform that can be adjusted to different levels of stability, allowing clinicians and researchers to evaluate an individual's ability to maintain balance under varying conditions.

Time frame
3 month

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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