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Comparing high altitude treatment with current best care in children with Atopic Dermatitis (AD) and asthma within the atopic syndrome by the Wilhelmina Children?s Hospital, Utrecht-Dutch Asthma Centre, DAVOS

Not Applicable
Completed
Conditions
Atopic dermatitis and asthma within the atopic syndrome
Skin and Connective Tissue Diseases
Atopic dermatitis
Registration Number
ISRCTN88136485
Lead Sponsor
niversity Medical Center Utrecht (UMCU) (Netherlands)
Brief Summary

1. 2014 protocol in: http://www.ncbi.nlm.nih.gov/pubmed/24670079 2. 2017 results in https://www.ncbi.nlm.nih.gov/pubmed/29121432 (added 31/01/2019) 3. 2018 results in: https://www.ncbi.nlm.nih.gov/pubmed/29575251 (added 01/10/2019)

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
80
Inclusion Criteria

1. Moderate to severe atopic dermatitis
2. 8-18 years
3. Be able to speak and write in Dutch
4. Internet access and be able to use the Digital Eczema Center Utrecht
5. Willing to stay for 6 weeks in the Dutch Asthma Centre Davos

Exclusion Criteria

Current participation in another study

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<br> Current primary outcome measures as of 03/12/2013:<br> 1. Disease coping and acceptance, measured with the COPEKI/JUCCKI questionnaire<br> 2. Disease-specific quality of life, measured with Children's Dermatology Life Quality Index (CDQLI)<br> 3. Self Administered Eczema Area and Severity Index (SA-EASI)<br> All measured before the intervention, directly after the intervention, 6 weeks after the intervention and 6 months after the intervention<br><br> Previous primary outcome measures:<br> 1. Disease coping and acceptance, measured with the COPEKI/JUCCKI questionnaire directly after the intervention and 6 months after the intervention<br> 2. Disease-specific quality of life, measured with Children's Dermatology Life Quality Index (CDQLI) directly after the intervention, 6 weeks after the intervention and 6 months after the intervention<br>
Secondary Outcome Measures
NameTimeMethod
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