Effectiveness of a web-based educational, quality of life intervention in non-segmental vitiligo patients: a randomized controlled trial.
Completed
- Conditions
- Non-segmental vitiligo10035023
- Registration Number
- NL-OMON42778
- Lead Sponsor
- Academisch Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 100
Inclusion Criteria
• Diagnosis of non-segmental vitiligo
• Patient visiting the NIPD during regular outpatient clinic visit and receives standard of care
• Skindex-29 emotions subscore of >= 35 and/or functioning subscores of >= 32 (moderate and severe impairment)
• Age of 18 years or older
• Patient is willing and able to give written consent
Exclusion Criteria
• No access to a computer with internet connection
• Mental and/or physical impairment that could obstruct participation in the study
• Psychiatric comorbidity (e.g. depression, anxiety disorders)
• Insufficient mastery of Dutch
• Participation in another study with HRQoL as primary outcome.
• Currently receiving psychological and/or psychiatric treatment.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p> Mean differences in emotion and functioning scores of the Skindex-29 between<br /><br>baseline and 3 or 6 months in both study groups. </p><br>
- Secondary Outcome Measures
Name Time Method <p>Secondary outcome measures are improvement on self-efficacy, coping strategies,<br /><br>feelings of stigmatisation and symptoms of depression and anxiety.</p><br>