Sensory Perceptual Training on Activities of Daily Living and Hand Functions

May 9, 2025 updated by: hanaa mohsen, Badr University

Effect of Sensory-Perceptual Motor Training on Activities of Daily Living and Hand Functions in Unilateral Cerebral Palsy

Many risk factors can come to the fore in CP. With the new studies on CP, new risk factors are defined and existing risks are better understood. In the light of current information, general risk factors for CP are defined as premature birth, fetal growth restriction, multiple pregnancies, infections in the fetal or neonatal period, birth asphyxia, perinatal stroke, and congenital developmental disorders In addition, related risk factors are classified as prenatal, perinatal and postnatal

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Children and youth with cerebral palsy face unique challenges when learning, practicing, and mastering activities of daily living (ADLs). Active participation in dressing, feeding, toileting, clothing management, and small space mobility is influenced by body structures and function and environmental and personal factors

Study Type

Interventional

Enrollment (Actual)

52

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 Locations

  • Egypt
      • Cairo, Egypt
        • Badr UNIVERSITY and Cairo University
      • Cairo, Egypt
        • BADR

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:

  • Modified Ashworth 1 and 1 +
  • GMFCS level I and II
  • Able to understand and follow instructions

Exclusion Criteria:

  • fixed contracture or deformities in the spine or extremities
  • visual or respiratory Problems,
  • orthopedic surgery

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
Other: control
physical therapy excersises
Other: physical therapy excersies
1- selected physical therapy exercises
Experimental: intervention
sensory perceptual training
Other: sensory perceptual motor exercises
selected sensory perceptual motor exercises

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Katz Index
Time Frame: pre and post treatment for 12 weeks
It was especially designed to evaluate activities of daily living
pre and post treatment for 12 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Jebsen Taylor Hand Function Test
Time Frame: pre and post treatment for 12 weeks
It was especially designed to evaluate Time motor performance
pre and post treatment for 12 weeks
box and block test
Time Frame: pre and post treatment for 12 weeks
It was especially designed to evaluate the gross manual dexterity
pre and post treatment for 12 weeks

Collaborators and Investigators

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

Sponsor

Badr University

Investigators

  • Principal Investigator: Hanaa mohsen, Associate professor

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 (Actual)

September 15, 2024

Primary Completion (Actual)

March 15, 2025

Study Completion (Actual)

April 30, 2025

Study Registration Dates

First Submitted

August 9, 2024

First Submitted That Met QC Criteria

August 12, 2024

First Posted (Actual)

August 15, 2024

Study Record Updates

Last Update Posted (Actual)

May 14, 2025

Last Update Submitted That Met QC Criteria

May 9, 2025

Last Verified

May 1, 2025

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Hanaa M

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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