Geneva, Sept. 21 -- International Clinical Trials Registry received information related to the study (NCT07815249) titled 'Speech Therapy for Children With Rare Genetic Conditions and Childhood Apraxia of Speech' on Sept. 6.
Study Type: Interventional
Study Design:
Allocation: N/A. Intervention model: Single Group Assignment. Primary purpose: Treatment. Masking: None (Open Label).
Primary Sponsor: Murdoch Childrens Research Institute
Condition:
Childhood Apraxia of Speech
Genetic Condition
Intervention:
Behavioral: Rapid Syllable Transition Treatment
Recruitment Status: Recruiting
Phase: N/A
Date of First Enrollment: July 1, 2026
Target Sample Size: 20
Countries of Recruitment:
Australia
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