Intervention Study to Evaluate the Importance of Information Given to Patients With Contact Allergy
Not Applicable
Completed
- Conditions
- Dermatitis, Allergic Contact
- Interventions
- Behavioral: extended information
- Registration Number
- NCT01953380
- Lead Sponsor
- Region Skane
- Brief Summary
The purpose of this study is to determine whether extended information given to patients with contact allergy improves knowledge, treatment efficacy and daily functioning.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 400
Inclusion Criteria
- Patients with suspected contact allergy
- Age above 18 years
- Participants have given informed consent
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Exclusion Criteria
- Mental or language disabilities
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Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description extended information extended information Extended information on specific allergy
- Primary Outcome Measures
Name Time Method knowledge one year after inclusion knowledge about specific contact allergies and exposure, assessed by questionnaire, a modified version of Nordic Occupational Skin Questionnaire NOSQ-2002/Long, and patient records.
- Secondary Outcome Measures
Name Time Method clinical improvement one year after inclusion assessed by questionnaire, a modified version of Nordic Occupational Skin Questionnaire NOSQ-2002/Long, and patient records.
quality of life one year after inclusion assessed by questionnaire, Dermatology Life Quality Index (DLQI).
effect on daily functioning one year after inclusion assessed by questionnaire, a modified version of Nordic Occupational Skin Questionnaire NOSQ-2002/Long, and Dermatology Life Quality Index (DLQI).
Trial Locations
- Locations (1)
Hudmottagningen SUS
🇸🇪Lund, Skåne, Sweden