Field testing of a Patient-Reported Outcome Measure for Cleft Lip and Palate: The CLEFT-Q
Completed
- Conditions
- 10040789cleft lip and palate
- Registration Number
- NL-OMON42276
- Lead Sponsor
- niversitair Medisch Centrum Groningen
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 200
Inclusion Criteria
* Children/adolescents with CL, CP, CLP between 6 and 29 years of age.
* Who gave written informed consent (and/or their parents in case of minors)
* who are under treatment in our centres or
* who had treatment in our centres in the past:
Exclusion Criteria
* Children with a cognitive disability and/or who cannot read.
* Children who do not understand/speak Dutch.
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Outcome of the study: An internationally validated PROM for use by patients<br /><br>with cleft lip and/or palate.</p><br>
- Secondary Outcome Measures
Name Time Method <p>Not applicable</p><br>