Effect of Imaginary Resisted Therapy Versus Physical Resisted Therapy on Hemiplegic Cerebral Palsy

NCT ID: NCT06001983

Last Updated: 2023-08-21

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

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

34 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-05-30

Study Completion Date

2023-09-20

Brief Summary

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The purpose of this study is to compare the effects of imaginary resisted exercises versus physical resisted exercises on hand grip strength in hemiplegic cerebral palsy

Detailed Description

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Cerebral palsy (CP) is one of the most frequent causes of motor disability in children. CP is a group of permanent disorders of the development of movement and posture, causing activity limitations that are attributed to non-progressive disturbances that occurred in the developing fetal or infant brain. The risk factors for CP can be divided into pre-conception, prenatal, perinatal and postnatal ones. Twenty five percent of children with CP have spastic hemiplegia. Hemiplegic cerebral palsy falls in anatomic classification of cerebral palsy which affects only one side of body. Children who have hemiplegic cerebral palsy have absolutely no use of one side of the body. This means their shoulder; arm, hand, leg and foot are all completely paralyzed. So, in order to improve strength in upper extremity and hand, resistance exercises are used.

The study will be a randomized control trial. Patients will be recruited into two groups using simple random assignment. Non probability convenient sampling will be used. Data will be collected from patients with hemiplegic cerebral palsy by using Jamar dynamometer which is consider as a gold standard in measuring repetitive gripping, goniometer for range of motion and Finger to nose test to access the upper extremity function in stroke patient Those who will meet the inclusion criteria will be recruited. Group A will receive imaginary resisted exercise therapy Five types of different resistances will be imagined by patients by watching their own videos in VR box, which will be recorded on day one to make them familiar with the resistive objects and the resistance experienced from them by asking patients to perform 15-15 repetitions of each object. Group B will receive physical resisted exercise therapy in which 5 different types of resistances will be given to patients for making themselves familiarize themselves with the type of resistance applied by each object, that they will experience in further sessions, by asking them to perform 15-15 repetitions of each object. Every physical resistance exercise will have 15 repetitions. At the end of each session patient will perform finger to nose test and Purdue peg board test. After collecting data from the defined setting, it will be entered and analyzed using statistical package for social sciences (SPSS) for Windows Software, version 21.

Conditions

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Hemiplegic Cerebral Palsy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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Imaginary resisted exercises

• Handgrip exercises with the imagination of resistance in hand by getting feedback in VR Box will be given as an intervention. Stretching will be given at the beginning and the end of each session. This will include imaginary resistance exercises for handgrip by using Virtual Reality Box. Five types of different resistances will be imagined by patients by watching their own videos in VR box, which will be recorded on day one to make them familiar with the resistive objects and the resistance experienced from them by asking patients to perform 15-15 repetitions of each object. Every imaginary resistance exercise will have 15 repetitions. After performing exercises, the participants will ask to perform Finger-to-Nose Test and Purdue Pegboard Test.

Group Type EXPERIMENTAL

imaginary resisted exercises

Intervention Type OTHER

1. Imagination of squeezing a Sponge ball 15 reps
2. Imagination of Finger Exerciser 15 reps
3. Imagination of Theraband 15 reps
4. Imagination of pressing Rubber ball 15 reps
5. Imagination of pressing Hard object 15 reps

Physical resisted exercises

Handgrip exercises with physical resistance in hand will be given as an intervention. Stretching will be given at the beginning and the end of the session. 5 different types of resistances will be given to patients for making themselves familiarize themselves with the type of resistance applied by each object, that they will experience in further sessions, by asking them to perform 15-15 repetitions of each object. Every physical resistance exercise will have 15 repetitions. After performing exercises, the participants will ask to perform Finger-to-Nose Test and Purdue Pegboard Test. In physical resistance exercises, resistive force is applied to the targeted region by using different and appropriate resistive objects

Group Type EXPERIMENTAL

physical resisted exercises

Intervention Type OTHER

1. Resisted exercise of Squeezing a Sponge ball 15 reps
2. Resisted exercise of Finger Exerciser 15 reps
3. Resisted exercise of pulling theraband 15 reps
4. Resisted exercise of pressing Rubber ball 15 reps
5. Resisted exercise of pressing Hard object 15 reps

Interventions

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imaginary resisted exercises

1. Imagination of squeezing a Sponge ball 15 reps
2. Imagination of Finger Exerciser 15 reps
3. Imagination of Theraband 15 reps
4. Imagination of pressing Rubber ball 15 reps
5. Imagination of pressing Hard object 15 reps

Intervention Type OTHER

physical resisted exercises

1. Resisted exercise of Squeezing a Sponge ball 15 reps
2. Resisted exercise of Finger Exerciser 15 reps
3. Resisted exercise of pulling theraband 15 reps
4. Resisted exercise of pressing Rubber ball 15 reps
5. Resisted exercise of pressing Hard object 15 reps

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Congenital infantile hemiplegia.
* Aged between 6 and 12 years.
* Lack of use of the affected upper limb.
* Level I-III of the Manual Ability Classification System (MACS).
* Students scoring of Modified Ashworth Scale should be 3 or less than 3 out of 5 for the same muscle groups of previously mentioned movements.

Exclusion Criteria

* Low cognitive level compatible with attending a special education school.
* Presence of contractures in the affected upper limb affecting the functional movement.
* Surgery in the six months previously to the treatment.
* Botulinum toxin in the two months previously to or during the intervention.
* Pharmacologically uncontrolled epilepsy
Minimum Eligible Age

6 Years

Maximum Eligible Age

12 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Riphah International University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Dr. Nosheen Manzoor, MS OMPT

Role: PRINCIPAL_INVESTIGATOR

Riphah International University

Locations

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Govt. National special education centre

Lahore, Punjab Province, Pakistan

Site Status RECRUITING

Countries

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Pakistan

Central Contacts

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Dr. Nosheen Manzoor, MS OMPT

Role: CONTACT

03236877879

Facility Contacts

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Naseer Khan

Role: primary

03076913927

Other Identifiers

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REC/RCR & AHS/23/0721

Identifier Type: -

Identifier Source: org_study_id

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