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Comparison of quality of life between children and teenagers with IBD and celiac disease - a survey among affected children and their parents

Conditions
K90.0
K50
K51
K52.3
Coeliac disease
Crohn disease [regional enteritis]
Ulcerative colitis
Indeterminate colitis
Registration Number
DRKS00027418
Lead Sponsor
niklinik Köln, Klinik und Poliklinik für Kinder- und Jugendmedizin, Kindergastroenterologie
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
119
Inclusion Criteria

Patients who are between 3 and 18 years old (and their parents) who have received a confirmed diagnosis of celiac disease respectively IBD in the department of paediatric gastroenterology and hepatology of the University Medical Centre Cologne and who are being treated here.

Exclusion Criteria

Missing letter of agreement to participate in the survey or its cancellation.

Study & Design

Study Type
observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Two validated and established (illness specific) questionnaires are used with the aim of measuring the patients' quality of life as well as identifying mainly impaired areas of it. <br>In addition and only to be filled out by the parents there is a questionnaire used for assessing socioeconomic status. <br>Answers can be given in physical form as well as online via a survey software. <br>The aim is to get 60 answers of each collective.
Secondary Outcome Measures
NameTimeMethod
Assessment of quality of life of pediatric children and adolescents with coeliac disease respectively inflammatory bowel diseases.
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