search  
 


Home

Who are we?

Why
register?


Signup for
registration


Online registration

Log in to register
your trial


Search a trial

NRT en CCMO

Contact

NEDERLANDS





MetaRegister
van CCT (UK)


ISRCTN-Register
van CCT (UK)


Field testing the CLEFT-Q


- candidate number21125
- NTR NumberNTR4934
- ISRCTNISRCTN no longer applicable
- Date ISRCTN created
- date ISRCTN requested
- Date Registered NTR8-dec-2014
- Secondary IDsNL 51730 
- Public TitleField testing the CLEFT-Q
- Scientific TitleField testing of a Patient-Reported Outcome Measure for Cleft Lip and Palate: The CLEFT-Q
- ACRONYM
- hypothesis
- Healt Condition(s) or Problem(s) studiedQuality of life, Patient reported outcomes, Schisis
- 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.
- mec approval receivedno
- multicenter trialyes
- randomisedno
- group[default]
- Type[default]
- Studytypeobservational
- planned startdate 16-jan-2015
- planned closingdate15-jun-2015
- Target number of participants200
- InterventionsSubjects will fill in a Patient reported outcome measure
- Primary outcomeOutcome of the study: An internationally validated PROM for use by patients with cleft lip and/or palate.
- Secondary outcomenot applicable
- Timepointsnot applicable
- Trial web site
- statusplanned
- CONTACT FOR PUBLIC QUERIES M. Dreise
- CONTACT for SCIENTIFIC QUERIES M. Dreise
- Sponsor/Initiator University Medical Center Groningen (UMCG)
- Funding
(Source(s) of Monetary or Material Support)
McMasters University, Canada
- Publications
- Brief summarySo far outcomes in cleft treatment have mainly been measured in objective and biomedical outcomes. Patient perspectives are often overlooked, because an appropriate, well-defined, valid, reliable and responsive Patient Reported Outcome measurement tool is not available. An international team of experts from Candada, USA and UK has taken up the challenge and is developing this PRO instrument, called the CLEFT-Q. The cleft team in the UMCG/MCL will take part in field testing the CLEFT-Q
- Main changes (audit trail)
- RECORD8-dec-2014 - 2-feb-2015


  • Indien u gegevens wilt toevoegen of veranderen, kunt u een mail sturen naar nederlands@trialregister.nl