The Hand Eczema Trial (HET): design of a randomised clinical trial of the effect of classification and individual counselling versus no intervention among health-care workers with hand eczema

被引:12
|
作者
Ibler, Kristina Sophie [1 ]
Agner, Tove [2 ]
Hansen, Jane Lindschou [3 ]
Gluud, Christian [3 ]
机构
[1] Roskilde Hosp, Dept Dermatol, Roskilde, Denmark
[2] Bispebjerg Hosp, Dept Dermatol, Copenhagen, Denmark
[3] Ctr Clin Intervent Res, Copenhagen Trial Unit, Copenhagen, Denmark
来源
BMC DERMATOLOGY | 2010年 / 10卷
关键词
D O I
10.1186/1471-5945-10-8
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Hand eczema is the most frequently recognized occupational disease in Denmark with an incidence of approximately 0.32 per 1000 person-years. Consequences of hand eczema include chronic severe eczema, prolonged sick leave, unemployment, and impaired quality of life. New preventive strategies are needed to reduce occupational hand eczema. Methods/Design: We describe the design of a randomised clinical trial to investigate the effects of classification of hand eczema plus individual counselling versus no intervention. The trial includes health-care workers with hand eczema identified from a self-administered questionnaire delivered to 3181 health-care workers in three Danish hospitals. The questionnaire identifies the prevalence of hand eczema, knowledge of skin-protection, and exposures that can lead to hand eczema. At entry, all participants are assessed regarding: disease severity (Hand Eczema Severity Index); self-evaluated disease severity; number of eruptions; quality of life; skin protective behaviour, and knowledge of skin protection. The patients are centrally randomised to intervention versus no intervention 1:1 stratified for hospital, profession, and severity score. The experimental group undergoes patch and prick testing; classification of the hand eczema; demonstration of hand washing and appliance of emollients; individual counselling, and a skin-care programme. The control group receives no intervention. All participants are reassessed after six months. The primary outcome is observer-blinded assessment of disease severity and the secondary outcomes are unblinded assessments of disease severity; number of eruptions; knowledge of skin protection; skinprotective behaviour, and quality of life. Trial registration: The trial is registered in ClinicalTrials. Gov, NCT01012453.
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页数:10
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