Psoriasis Clinical Trial
— DEVISEOfficial title:
DEVISE - Development and Evaluation of an Online Intervention to Reduce Self-stigma in People With Visible Chronic Skin Diseases: a Randomized Controlled Trial
NCT number | NCT06324695 |
Other study ID # | 01GY2105 |
Secondary ID | |
Status | Not yet recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | March 2024 |
Est. completion date | March 2025 |
This project aims to develop and evaluate an online intervention to prevent and/or reduce self-stigma in German patients with visible chronic skin diseases. Evaluation of the intervention with regard to effectiveness and feasibility will follow an open-label randomized controlled design with 550 patients in total. The results of the program are expected to provide new insights and markedly extended knowledge on the mechanisms of self-stigma in chronic skin conditions. The new online intervention can be used in routine care, aiming for better patient care in practice and, ultimately decreased extent of self-stigma, increased quality of life of patients, and decreased rates of depression, anxiety, and suicide ideation.
Status | Not yet recruiting |
Enrollment | 550 |
Est. completion date | March 2025 |
Est. primary completion date | September 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Clinical diagnosis of psoriasis, atopic dermatitis, hidradenitis suppurativa, alopecia areata, or vitiligo; - Age = 18 years; - Sufficient language skills (German) to follow the instructions and content of the intervention; - Access to a desktop/ laptop with internet connection; - Having signed an Informed Consent Form (ICF). Exclusion Criteria: - Age < 18 years; - Lack of informed consent (ICF); - Patients that were treated in the last 12 months by a psychologist, psychotherapist, or psychiatrist for major depression, schizophrenia or other psychotic disorder, major bipolar disorder, major anxiety or obsessive-compulsive disorder, post-traumatic stress disorder, or major personality disorder. |
Country | Name | City | State |
---|---|---|---|
Germany | Deutscher Vitiligo-Bund e.V. | Adelsdorf | |
Germany | Fachklinik Bad Bentheim, Fachbereich Dermatologie und Allergologie | Bad Bentheim | |
Germany | Universitätsklinikum der Ruhr-Universität Bochum (UKRUB), Klinik für Dermatologie, Venerologie und Allergologie | Bochum | |
Germany | Deutscher Psoriasis Bund e.V. (DPB) | Hamburg | |
Germany | Hautarztpraxis Dr. Daniela Kasche | Hamburg | |
Germany | Universitätsklinikum Hamburg-Eppendorf (UKE), Institut für Versorgungsforschung in der Dermatologie und bei Pflegeberufen (IVDP) | Hamburg | |
Germany | Universitätsklinikum Schleswig-Holstein, Klinik für Dermatologie, Venerologie und Allergologie, Psoriasis-Zentrum-Kiel | Kiel | |
Germany | Alopecia Areata Deutschland e.V. | Krefeld | |
Germany | Universitätsmedizin der Johannes-Gutenberg-Universität Mainz, Hautklinik und Poliklinik | Mainz | |
Germany | Technische Universität München, Klinik und Poliklinik für Dermatologie und Allergologie am Biederstein | München | |
Germany | Universitätsklinikum Münster (UKM), Klinik für Hautkrankheiten - Allgemeine Dermatologie und Venerologie | Münster | |
Germany | Dermatologische Spezial- und Schwerpunktpraxis Dr. med. Ralph von Kiedrowski | Selters | |
Germany | Privatpraxis Dr. med. Matthias Hoffmann | Witten |
Lead Sponsor | Collaborator |
---|---|
Universitätsklinikum Hamburg-Eppendorf | German Federal Ministry of Education and Research |
Germany,
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* Note: There are 45 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Changes from baseline to post-intervention and follow-up in illness identity | Evaluated with the Inclusion of Illness in the Self (IIS) scale. Respondents indicate in a single item the degree to which their illness is integrated into their self-concept. The higher the IIS score, the greater patients felt they internalized their illness. | Baseline (t0), immediately post-intervention (t1), 6-months follow-up (t2) | |
Other | Changes from baseline to post-intervention and follow-up in avoidance and acceptance coping | Evaluated with the subscales avoidance (8 items) and positive rational acceptance (11 items) of the Body Image Coping Strategies Inventory (BICSI). The 19 items are answered in a Likert-type response scale ranging from 0 to 3, and an average score is calculated for each subscale, with higher scores indicating more frequent use of the specific coping strategy. | Baseline (t0), immediately post-intervention (t1), 6-months follow-up (t2) | |
Other | Changes from baseline to post-intervention and follow-up in generic body image/ appearance concerns | Evaluated with the Appearance Orientation Subscale of the Multidimensional Body-Self Relations Questionnaire (MBSRQ-AO). This subscale includes 2 items, to be answered on a 5-point Likert scale. The average score for the subscale is computed, with higher scores indicating more appearance concerns. | Baseline (t0), immediately post-intervention (t1), 6-months follow-up (t2) | |
Other | Changes from baseline to post-intervention and follow-up in cutaneous body image | Evaluated with the Cutaneous Body Image Scale (CBIS), which comprises 7 items, to be rated on a response scale from 0 ("not at all") to 9 ("very markedly"). A composite score is derived from the mean ratings of the seven items, where a high score is indicative of greater satisfaction with cutaneous body image: score < 3 = severe dissatisfaction; 3-6 = moderate dissatisfaction; > 6 = mild to no dissatisfaction. | Baseline (t0), immediately post-intervention (t1), 6-months follow-up (t2) | |
Other | Changes from baseline to post-intervention and follow-up in self-compassion | Evaluated with the short version of the Self-Compassion Scale (SCS), which includes 12 items, to be answered in a 5-point response scale ranging from 1 ("Almost never") to 5 ("Almost always"). Mean scores can be computed for six subscales - Self-Kindness, Self-Judgment (reversed scoring), Common Humanity, Isolation (reversed scoring), Mindfulness, and Over-identification (reversed scoring), as well as a total self-compassion score that results from the average of the six subscale mean scores, with higher scores indicating higher levels of self-compassion. | Baseline (t0), immediately post-intervention (t1), 6-months follow-up (t2) | |
Other | Session Feedback | Evaluated with an ad hoc questionnaire that comprises 3 questions tapping into whether the session just completed was interesting, easy to understand, and personally helpful. Respondents are asked to answer the questions on a 5-point Likert scale, where higher scores represent greater agreement. | At the end of each session of the program | |
Primary | Changes from baseline to post-intervention and follow-up in self-stigma | Evaluated with the Weight Bias Internalization Scale (WBIS) - adapted for skin disease. The scale includes 10 items with a Likert-type response scale ranging from 1 to 7 and provides a total sum score ranging from 10 to 70, with higher scores indicating higher internalization of stigma and biases associated with own skin disease. | Baseline (t0), immediately post-intervention (t1), 6-months follow-up (t2) | |
Secondary | Changes from baseline to post-intervention and follow-up in generic quality of life | Evaluated with the EUROHIS-QOL 8-item index. The instrument includes 8 items assessing overall QOL, general health, energy, daily life activities, esteem, relationships, finances, and home environment, to be scored on a 5-point Likert scale. A total score is generated, with higher scores indicating better quality of life. | Baseline (t0), immediately post-intervention (t1), 6-months follow-up (t2) | |
Secondary | Changes from baseline to post-intervention and follow-up in skin-generic quality of life | Evaluated with the Dermatology Life Quality Index (DLQI), which includes 10 items, to be answered on a 4-point Likert scale ranging from 0 ("not at all"/ "not relevant") to 3 ("very much"). A total sum score ranging from 0 to 30 is computed, with higher scores indicating larger impairments. According to the Hongbo classification, DLQI scores > 10 are considered as large or extremely large impairments on patients' life. | Baseline (t0), immediately post-intervention (t1), 6-months follow-up (t2) | |
Secondary | Changes from baseline to post-intervention and follow-up in depression | Evaluated with the nine-item Patient Health Questionnaire (PHQ-9), which is a validated screening measure for diagnosing and monitoring depression. The response scale ranges from 0 ("not at all") to 3 ("nearly every day"); the sum score ranges from 0 to 27 and a cut-off point = 10 has showed maximized sensitivity and specificity to detect major depression. | Baseline (t0), immediately post-intervention (t1), 6-months follow-up (t2) | |
Secondary | Changes from baseline to post-intervention and follow-up in anxiety | Evaluated with the General Anxiety Disorder (GAD-7), which is a brief validated instrument to screen for anxiety disorders. It comprises seven items that represent core anxiety symptoms. The response scale ranges from 0 ("not at all") to 3 ("nearly every day"); the 7 items can be summed into a total score ranging from 0 to 21, with scores = 10 indicating high likelihood of clinical anxiety disorders. | Baseline (t0), immediately post-intervention (t1), 6-months follow-up (t2) | |
Secondary | Changes from baseline to post-intervention and follow-up in suicidal ideation | Evaluated with Paykel's Suicidal Feelings in the General Population Questionnaire, which is one of the most widely used measures of suicidal ideation in different populations, including medical settings. It comprises 5 questions about life-weariness, death wishes, and suicidal thoughts, plans and attempts, to be answered in a yes/no response scale. A "yes"-response to questions 3 to 5 indicates the presence of suicidal ideation. | Baseline (t0), immediately post-intervention (t1), 6-months follow-up (t2) | |
Secondary | Feasibility of the HautKompass online program | Measured through general statistics of website utilization (e.g., time spent on each session). Durations of individuals sessions of > 45 minutes are considered not feasible for implementation. | continuously tracked during intervention | |
Secondary | Feasibility of the HautKompass online program - dropouts | Measured through dropout rate. | continuously tracked during intervention | |
Secondary | User satisfaction with the HautKompass online program | Evaluated with the Client Satisfaction Questionnaire Adapted to Internet-Based Interventions (CSQ-I), which includes 8 questions on a Likert scale of 1 to 4, with higher scores indicating greater satisfaction. | Immediately post-intervention (t1) | |
Secondary | Acceptability of the HautKompass online program | Evaluated with an ad hoc questionnaire that comprises 5 questions about the general acceptability of the website. Respondents are asked to answer the questions on a 4-point Likert scale, where higher scores represent higher acceptability. | Immediately post-intervention (t1) |
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