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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT02205593
Other study ID # Haut-Tief
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date July 2012
Est. completion date December 2022

Study information

Verified date July 2019
Source University of Zurich
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

'Haut-Tief' (Skin Deep) is an educational, stress reducing program for patients with psoriasis or atopic dermatitis. A range of support activities will be offered in order to learn effective self-management strategies and attitude to one's chronic skin disease and consequently improving quality of life.


Description:

The educational program consists of 2-hours of educational (dermatology, specialized nurse, psychologist) and stress-reduction sessions (yoga, meditation, physiotherapy) twice a week during 9 weeks.

A multidisciplinary team of trainers is involved. Primary endpoint is the general and skin dependent quality of life measured by questionnaires. HRQoL (Health-Related Quality of Life) is measured at baseline, after 3 months, 6 months and 9 months follow up. Patients are recruited from the out-patient clinic at the Department of Dermatology of the University Hospital Zurich. Patients are randomized in an intervention and control group. Intervention group receives the education program additionally to follow-up visits whereas the control group receives follow-up visits. Several runs are planned.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 80
Est. completion date December 2022
Est. primary completion date October 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- Chronic psoriasis (disease for more than 3 months)

- Chronic eczema (disease for more than 3) months)

- Age = 18 years

- Oral and written informed consent

Exclusion Criteria:

- systemic antiinflammatory therapy

- treatment with other investigational products

- other clinically significant concomitant disease states (e.g., renal failure, hepatic dysfunction, cardiovascular disease, etc),

- known or suspected non-compliance, drug or alcohol abuse,

- inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia or confusional state of the subject

- participation in another study within the 30 days preceding and during the present study, (viii) previous enrollment into the current study,

- enrolment of the investigator, his/her family members, employees and other dependent persons.

Study Design


Intervention

Behavioral:
Control
Regular follow-up and treatment WITHOUT behavioural intervention

Locations

Country Name City State
Switzerland University Hospital Zurich, Department of Dermatology Zurich ZH

Sponsors (1)

Lead Sponsor Collaborator
University of Zurich

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary change in DLQI (Dermatology Life Quality Index) score [ ] DLQI is a questionnaire measuring Health related quality of life 10 questions baseline, 3 months, 6 months, 9 months
Primary change in Skindex-29 score [ ] Questionnaire measuring Health related quality of life 29 questions baseline, 3 months, 6 months, 9 months
Primary change in ShortForm 36 score [ ] Questionnaire measuring Health related quality of life baseline, 3 months, 6 months, 9 months
Primary change in EQ 5D score [ ] Questionnaire measuring Health related quality of life baseline, 3 months, 6 months, 9 months
Primary change in EQ VAS (EQ visual analogue scale) score [ ] Questionnaire measuring Health related quality of life baseline, 3 months, 6 months, 9 months
Secondary change in EASI (eczema area and severity index) score [ ] clinical score for atopic dermatitis baseline, 3 months, 6 months, 9 months
Secondary change in PASI (psoriasis area and severity index) [ ] clinical score for psoriasis baseline, 3 months, 6 months, 9 months
Secondary BDI (Beck Depression Inventory) score [ ] baseline, 3 months, 6 months, 9 months
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