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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03903263
Other study ID # Req-2018-00772; sp19Mueller
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 21, 2018
Est. completion date January 31, 2019

Study information

Verified date April 2019
Source University Hospital, Basel, Switzerland
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study is to investigate sleep disorders in patients with dermatologic diseases by taking into consideration dermatologic (itch, pain) and non- dermatologic (medication, depression) factors.


Recruitment information / eligibility

Status Completed
Enrollment 624
Est. completion date January 31, 2019
Est. primary completion date January 31, 2019
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Outpatients of the dermatologic university clinic

Exclusion Criteria:

- Insufficient knowledge of German language

- Illiteracy

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
survey on sleep disorders
self-administered patient questionnaire regarding the different aspects of sleep disorders in patients with dermatologic diseases

Locations

Country Name City State
Switzerland Department of Dermatology, University Hospital Basel Basel

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Basel, Switzerland

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Regensburg Insomnia Scale (RIS) Self-rating scale: Five items cover quantitative and qualitative sleep parameters: Sleep latency (1), sleep duration (2), sleep continuity (3), early awakening (4) and sleep depth (5). Four items cover the psychological aspects of psychophysiological insomnia (PI), such as the experience of sleepless nights (6), focussing on sleep (7), fear of insomnia (8), and daytime fitness (9), one item covers sleep medication (10). A 5-step Likert scale was provided for response.The total score ranges from 0 to 40 points (score from 0-12 points considered as normal and a higher score as indicative of PI symptoms). single time point assessment at baseline
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