Sensory Motor Integration Training in Erb's Palsy Childern

March 15, 2024 updated by: Sara Elsayed Ali Abdelnaby Ali

Effect of Sensory Motor Training on Activities of Daily Living in Erb's Palsy Childern

The aim of the study is to Study effect of sensory motor integration training on ADL activities in children with Erb's palsy.

Study Overview

Status

Not yet recruiting

Detailed Description

Thirty-two participants , their age ranged from two to six years for both genders (sixteen children treated with designed occupational therapy program group A and sixteen treated with designed occupational therapy program and sensory motor integration training group B )

Study Type

Interventional

Enrollment (Estimated)

35

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  1. Their ages will be ranged from 2 to 6 years in both sexes.
  2. The infants with Erb's palsy (C5-C6).
  3. Can follow verbal commend
  4. Muscle tone within normal and muscle power within functional range.
  5. Intact vision and hearing.

Exclusion Criteria:

  1. Children undergoing surgical treatment.
  2. Cognitive problem and cognitive anomalies.
  3. Children with Erb's engram.
  4. Complete sensory loss.
  5. Shoulder subluxation or dislocation.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Use Designed occupational therapy program in childern with erb's palsy
1st group treated by strengthening exercises , stretching ,and occupational therapy
one group treated by strengthening exercises , stretching ,and occupational therapy and other group treated by strengthening exercises , stretching ,and occupational therapy and sensory motor integration training
Experimental: Use designed occupational therapy program and sensory motor integration training
2nd group treated by strengthening exercises , stretching ,and occupational therapy and sensory motor integration training (use different textures and different temperature)
one group treated by strengthening exercises , stretching ,and occupational therapy and other group treated by strengthening exercises , stretching ,and occupational therapy and sensory motor integration training

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Effect of sensory motor integration training on ADL
Time Frame: 3 months
Assessment of bimanual performance and family-reported upper-extremity use by Assisting Hand Assessment
3 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Sara Elsayed ali abdelnaby, Bachelor's, Kafrelsheikh University
  • Study Chair: Abd Elaziz Ali sherif, Professor of pediatric department- Faculty of physical therapy- kafrelsheikh university
  • Study Chair: Osama Abd Elfattah El-Agamy, professor and head of department of pedateric-faculty of medicine -kafrelsheik university
  • Study Director: Sara Yousef Abdel Elglil Elsebahy, Lecturer of pediatric department -Faculty of physical therapy- Kafrelshiekh University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

April 1, 2024

Primary Completion (Estimated)

April 1, 2025

Study Completion (Estimated)

April 1, 2025

Study Registration Dates

First Submitted

March 15, 2024

First Submitted That Met QC Criteria

March 15, 2024

First Posted (Actual)

March 22, 2024

Study Record Updates

Last Update Posted (Actual)

March 22, 2024

Last Update Submitted That Met QC Criteria

March 15, 2024

Last Verified

March 1, 2024

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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