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Clinical Trials/NCT06407349
NCT06407349CompletedNot Applicable

Effect of Communication Board on Functional Communication of Children With Cerebral Palsy

Riphah International University2 sites in 1 country20 target enrollmentStarted: May 6, 2024Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
20
Locations
2
Primary Endpoint
Functional Communication

Study Overview

Brief Summary

My aim of the research is to compare the effect of traditional therapy with the AAC device and identify if the AAC device is more effective for CP children than traditional therapy.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Participant)

Eligibility Criteria

Ages
8 Years to 12 Years (Child)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Children of both genders with Cerebral Palsy age group 8 years-12 years
  • Children with Cerebral Palsy having mild to moderate cognitive impairment and communication impairment
  • Children with comorbid conditions (epilepsy, microcephalia)
  • Children with physical abilities of functional Pointing, One Step Command
  • Following, Vocalization, and Imitation.

Exclusion Criteria

  • Children with comorbid conditions (visual impairment, hearing impairment

Outcomes

Primary Outcomes

Functional Communication

Time Frame: 8th week

Baseline measurement of all the individuals who are enrolled in the study will be taken by using the following assessment tools. Functional communication checklist; provide the score with reference to five domains- method of communication, communication interaction, communication function, expressive language skills, and receptive language skills Communication effective index will also be used which consists of sixteen items. Information Carrying words will be used based on age. After baseline measurements communication board intervention will be given to the individuals with cerebral palsy belonging to the experimental group while traditional therapy will be given to the control group. After providing the mentioned treatment to both groups for twenty four sessions, the post-assessment will be taken.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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