Grant: Project Grant
McMaster University
$378,427.00
An International Study to Develop a Patient-Reported Outcome Instrument for Conditions Associated with a Facial Difference: FACE-Q Kids
EF 2015-16
Résumé
Patient-reported outcome instruments (PROs) are questionnaires that measures patient concerns about their health by asking them directly. In surgery, the patient's perspective is particularly relevant as many key outcomes require the patient to self-report. For patients, surgeons and healthcare managers to make well-informed decisions, reliable and meaningful PRO data are needed. Our team is internationally known for creating a series of PRO instruments for adult plastic and reconstructive surgery patients. Our methods include a systematic review (Phase I), a qualitative study (Phase 2) and an international field test (Phase 3). To address the shortage of PROs for pediatric plastic surgery patients, we recently created FACE-Q Kids. This PRO instrument covers the concerns of patients who have conditions associated with a facial difference, including ear anomalies, facial paralysis and skeletal and soft tissue conditions. FACE-Q Kids is composed of 21 independently functioning scales that measure facial appearance, quality of life and facial function. Our GOAL is to finish the development of FACE-Q Kids. Our specific AIMS are: (1) field test FACE-Q Kids in Canada, USA and UK; (2) train/mentor new PRO scientists; and (3) promote the use of FACE-Q Kids through knowledge translation and exchange activities. Data will be collected from 624 patients aged 8-25 years and from 4 pediatric centres each in Canada, USA and UK (n=12). Patients will be invited to complete FACE-Q Kids scales directly into a web-based database (REDCap). The analysis will aim to identify the best subset of items to keep in the final version of FACE-Q Kids.
Programme
Project Grant
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
345118
Name
Klassen Anne F
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Health Services and Policy Research
Theme2
Health systems / services
Prcname2
Project Grant Competition
Projecttitle
An International Study to Develop a Patient-Reported Outcome Instrument for Conditions Associated with a Facial Difference: FACE-Q Kids
Programtype2
Operating Grants
Orgnameinp2
McMaster University
Cihramount2
$378,427
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Appearance; Craniofacial; Health Services Research; Outcomes; Patient-Reported Outcome; Plastic Surgery; Psychometrics; Quality Of Life; Rasch Measurement Theory; Surgery
Abstract
Patient-reported outcome instruments (PROs) are questionnaires that measures patient concerns about their health by asking them directly. In surgery, the patient's perspective is particularly relevant as many key outcomes require the patient to self-report. For patients, surgeons and healthcare managers to make well-informed decisions, reliable and meaningful PRO data are needed. Our team is internationally known for creating a series of PRO instruments for adult plastic and reconstructive surgery patients. Our methods include a systematic review (Phase I), a qualitative study (Phase 2) and an international field test (Phase 3). To address the shortage of PROs for pediatric plastic surgery patients, we recently created FACE-Q Kids. This PRO instrument covers the concerns of patients who have conditions associated with a facial difference, including ear anomalies, facial paralysis and skeletal and soft tissue conditions. FACE-Q Kids is composed of 21 independently functioning scales that measure facial appearance, quality of life and facial function. Our GOAL is to finish the development of FACE-Q Kids. Our specific AIMS are: (1) field test FACE-Q Kids in Canada, USA and UK; (2) train/mentor new PRO scientists; and (3) promote the use of FACE-Q Kids through knowledge translation and exchange activities. Data will be collected from 624 patients aged 8-25 years and from 4 pediatric centres each in Canada, USA and UK (n=12). Patients will be invited to complete FACE-Q Kids scales directly into a web-based database (REDCap). The analysis will aim to identify the best subset of items to keep in the final version of FACE-Q Kids.
Competitiondate
201603
Approvedterm2
2 yrs 0 mth
Pinamesdelim
Klassen, Anne F; Wong, Karen
Approvedterm
2 ans 0 mois
Cihrcontribution2
~ $378,427~ $0~