Cleft Lip and Palate Clinical Trials

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High and Low Intensity Speech Intervention in Children With a Cleft Palate: Perceptions of Children, Their Parents and Speech-language Pathologists

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Observational
SUMMARY

A cleft (lip and) palate 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 a cleft (lip and) palate based on the perceptions of the providers of the intervention (primary care speech-language pathologists) and the recipients of the intervention (children with a cleft (lip and) palate and their parents). 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, any secondary surgery and otological/audiological data will be collected from the medical records of the children with a cleft (lip and) palate. Based on this qualitative study, possible adjustments to the high-intensity therapy protocol can be made. In doing so, these modifications will be relevant to these key stakeholders. This will also facilitate the implementation and widespread use of high-intensity speech therapy in clinical speech therapy practice.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 4
Healthy Volunteers: f
View:

• Belgian Dutch-speaking children with a cleft palate with or without a cleft lip

• Aged between 4 and 12 years,

• Presence of at least one compensatory speech error in their speech based on the perceptual assessment of one experienced speech-language pathologist

Locations
Other Locations
Belgium
University Hospital Ghent
RECRUITING
Ghent
Contact Information
Primary
Tara Mouton
tara.mouton@ugent.be
+32496446308
Time Frame
Start Date: 2025-03-01
Estimated Completion Date: 2027-12
Participants
Target number of participants: 45
Treatments
High-intensity speech therapy (HISI)
Participants who received high-intensity speech therapy, consisting of five 30-minute sessions per week during two separate 2-week intervention periods, with a 6-week rest period between intervention periods.
Low-intensity speech therapy (LISI)
Participants who received low-intensity speech therapy, consisting of two 30-minute sessions per week over a 10-week intervention period.
Related Therapeutic Areas
Sponsors
Leads: University Ghent
Collaborators: Research Foundation Flanders

This content was sourced from clinicaltrials.gov