Using the Paediatric Gastroesophageal Reflux Disease Symptom and Quality of Life Questionnaire (PGSQ) in Children With Cerebral Palsy: a Preliminary Validation Study
Status: Recruiting
Location: See all (2) locations...
Study Type: Observational
SUMMARY
This study assesses the content validity of the PGSQ for parents/carer of children with cerebral palsy and GORD, including features such as readability, face validity and acceptability for completion. This will be done via 6 interviews, with the PGSQ being altered as identified as required. Reliability (test-retest) of the adapted version of the PGSQ being assessed with a sample of 20 parents/carers.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 2
Maximum Age: 16
Healthy Volunteers: f
View:
• Parents or carers of children with cerebral palsy (GMFCS level III-V) with symptoms of GORD or on treatment for presumed GORD, aged between 2-16 years.
Locations
Other Locations
United Kingdom
Poole Hospital
RECRUITING
Poole
Poole Hospital NHSFT
RECRUITING
Poole
Contact Information
Primary
Lee Tbaily
researchsponsorship@uhd.nhs.uk
+44 (0)1202 442025
Time Frame
Start Date: 2021-01-22
Estimated Completion Date: 2024-03
Participants
Target number of participants: 26
Treatments
Phase 1: Content Validity Testing
Cohort of 6 parents/carers of children with cerebral palsy and GORD, who will be interviewed regarding the content validity of the PGSQ when used to assess symptoms of GORD in children with cerebral palsy.
Phase 2: Reliability (test-retest) Testing
Cohort of 20 parents/carers of children with cerebral palsy and GORD, who will review and complete the adapted version of the PGSQ (post Phase 1) at two time points, two weeks apart.
Related Therapeutic Areas
Sponsors
Leads: Poole Hospital NHS Foundation Trust
Collaborators: British Society of Paediatric Gastroenterology, Hepatology and Nutrition