Effectiveness of Visual and Auditory Feedback on Eye-hand Coordination in Children With Hemiplegic Cerebral Palsy
1 other identifier
interventional
45
1 country
1
Brief Summary
The aim of this study was to investigate potential benefits of adding augmented biofeedback training to standard therapy in improving eye-hand coordination in children with hemiplegic cerebral palsy .Participants were divided randomly into three equal groups. Group (A) received specially designed program of physical therapy intervention strategies to facilitate visual motor integration and visual perception over a period of three months. Group (B) received augmented biofeedback training only, and group (C) received augmented biofeedback training and same physical therapy program as group (A).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jul 2018
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 1, 2018
CompletedFirst Submitted
Initial submission to the registry
November 10, 2018
CompletedFirst Posted
Study publicly available on registry
November 15, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 20, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
January 1, 2019
CompletedNovember 15, 2018
November 1, 2018
6 months
November 10, 2018
November 14, 2018
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change from Baseline Peabody Developmental Motor Scale at 3 months (2nd edition) (PDMS-2)
Peabody Developmental Motor Scale provides assessment and training or remediation of gross and fine motor skills for children. It composed of two scores (Gross Motor and Fine Motor) divided into six subtests (Reflexes, Stationary, Locomotion, Object Manipulation, Grasping, Visual-Motor Integration). scale ranges from 2, 1, or 0 ( 2 is the better outcome, 0 is the worse outcome)
10-15 minutes total, it is taken at base line and after 3 months of treatment
Study Arms (3)
group A
ACTIVE COMPARATORGroup (A) physical therapy program for 60 minutes per session, three times a week for three consecutive months
group B
ACTIVE COMPARATORGroup (B) E-Link Upper Limb Exerciser (augmented biofeedback training)for 60 minutes per session, three times a week for three consecutive months
group C
EXPERIMENTALgroup (C) physical therapy program and E-Link Upper Limb Exerciser
Interventions
this group received specially designed physical therapy program to facilitate eye-hand coordination and fine motor to improve VMI, VP and MC, which included: unbutton buttons, and button in all again; put the pellets in the bottle as fast as he/she can; place the shapes on its form board; build steps, wall, pyramid and a tower from cubes; cut out a line, square, triangle, and rectangular shapes on a paper by scissor; string squared cubes and lace the holes of strip. Children were trained for 60 minutes per session, three times a week for three consecutive months.
The exercises in the E-Link Upper Limb Exerciser System are in the form of simple and exciting games such as soccer, hitting walls, space shooting, driving, arnd throwing balls into a bucket.Children were trained for 60 minutes per session, three times a week for three consecutive months
physical therapy program and E-Link Upper Limb Exerciser. Children were trained for 60 minutes per session, three times a week for three months
Eligibility Criteria
You may qualify if:
- Grade of spasticity between 1 to 1+ according to Modified ashworth Scale,
- The ability to handle objects independently was between level (I) and (II)
- According to Manual Ability Classification System (MACS)
- No history of epilepsy
- No botulinum toxin A treatment for the upper extremities in the previous 6 months
- Able to understand and follow verbal commands and instructions
You may not qualify if:
- Presence of visual or auditory impairments
- Significant tightness or fixed deformities in the upper limbs
- Severe spasticity
- Autism
- Severe cognitive impairment
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Disabled Children's Association
Riyadh, 25058, Saudi Arabia
Study Officials
- PRINCIPAL INVESTIGATOR
Reem M Alwhaibi, PhD
Princess Nourah Bint Abdulrahman University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- associate professor
Study Record Dates
First Submitted
November 10, 2018
First Posted
November 15, 2018
Study Start
July 1, 2018
Primary Completion
December 20, 2018
Study Completion
January 1, 2019
Last Updated
November 15, 2018
Record last verified: 2018-11
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP, ICF, CSR, ANALYTIC CODE
- Time Frame
- 12 months after study completion
- Access Criteria
- data access requests will be reviewed by an external independent review panel. requestors will be required to sign a data access agreement.
data from participants will be made available