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The Effects of Oral Facial Facilitation and Oral Motor Therapy in Dysphagia

Not Applicable
Not yet recruiting
Conditions
Dysphagia
Spastic Cerebral Palsy (sCP)
Registration Number
NCT06785220
Lead Sponsor
Kafrelsheikh University
Brief Summary

The objective of this research is to investigate the impact of oral facial facilitation and oral motor therapy dysphagia in individuals with spastic cerebral palsy. Specifically, the study aims to:

* Evaluate changes in dysphagia and severity following a regimen of oral motor therapy and oral facial facilitation.

* Assess improvements in swallowing function, including ease of swallowing and reduction in dysphagia symptoms, after implementing oral motor therapy and oral facial facilitation.

Detailed Description

Not available

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
13
Inclusion Criteria
    1. Confirmed diagnosis of spastic cerebral palsy (CP) by a qualified medical professional.

    2. Participants aged 3 to 7 years, as this is a common demographic affected by spastic CP.

    3. Clinical diagnosis of dysphagia, confirmed by a speech-language pathologist or related healthcare provider.

    4. No recent significant changes in neurological status or medical condition within the last six months.

    5. Sufficient cognitive ability to follow simple instructions during therapy sessions, as assessed by a qualified professional.

    6. Parental or guardian consent obtained for participants under 18, along with assent from participants when appropriate.

    7. No recent (within the last three months) oral motor therapy interventions that could confound results.

    8. Willingness and ability of the participant to engage in therapy sessions consistently.

    9. Clearance from a physician to participate in oral motor therapy and related interventions.

Exclusion Criteria
    1. Diagnosis of other neurological disorders or conditions that may affect swallowing or motor skills.

    2. Serious medical conditions or comorbidities that could interfere with therapy (e.g., severe respiratory issues).

    3. Any surgical interventions affecting the oral or pharyngeal region within the last year.

    4. Concurrent participation in other clinical trials or interventions that could affect swallowing outcomes.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
functional oral intake scalethrough study completion, an average of 6 months
Simplified dysphagia severity rating scalethrough study completion, an average of 6 months
Eating Assessment Tool-10through study completion, an average of 6 months
Secondary Outcome Measures
NameTimeMethod
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