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Study identifier: NCT06895395 Synced from ClinicalTrials.gov · July 28, 2026
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High and Low Intensity Speech Intervention in Children With a Cleft Palate: Perceptions of Children, Their Caregivers and Speech-language Pathologists

Condition: Cleft Lip and Palate · Speech Disorders in Children  ·  Sponsor: University Ghent

PhaseN/A
Planned participants175
Who can joinAll sexes, 4 Years to 12 Years
Healthy volunteersNo

About this study

A cleft (lip and) palate (CP±L) is the most common congenital abnormality of the face and skull with a significant social impact, affecting speech, hearing, feeding, oral behavior, dentition and satisfaction with appearance. These consequences have a long-term and negative impact on social integration and well-being. The World Health Organization (WHO) highlights the significant financial costs, including morbidity, health care costs, emotional distress and social exclusion for patients, their families and society. The purpose of this study is to compare high- and low-intensity speech intervention in children with CP±L based on the perceptions of the providers of the intervention (primary care speech-language pathologists) and the recipients of the intervention (children with CP±L and their caregivers). Individual semi-structured interviews will be conducted with both intervention providers and recipients to explore perceptions and experiences, as well as acceptability of the two speech intervention intensities. Potential participants will be told that the interview will be recorded. The actual interviews will take place at a location and time that is most convenient for the participants. Each interview will be recorded using a Roland R-05 high-quality audio recorder. After conducting the interviews, all participants will be asked to complete a questionnaire regarding their demographics. In addition, data regarding the type of cleft, time and manner of closure of the cleft, a…

This description comes directly from the study's public registry record.

Talk to the study team

Tara Mouton  ·  +32 496 44 63 08  ·  tara.mouton@ugent.be

Always discuss trial participation with your own doctor first.

Locations (1)

Ghent University HospitalGhent, BelgiumRecruiting

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Source record: clinicaltrials.gov/study/NCT06895395