Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
72 participants
INTERVENTIONAL
2022-11-15
2026-05-15
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
OTHER
NONE
Study Groups
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MBSR (Mindfulness-Based Stress Reduction) group
MBSR (Mindfulness-Based Stress reduction) program : 1 weekly session of 2 hours and a half for 8 weeks, (first and last session: 3 hours) and an optional day of intensive practice of 6 hours, supervised by an MBSR instructor.
MBSR (Mindfulness-Based Stress Reduction)
MBSR (Mindfulness-Based Stress reduction) program : 1 weekly session of 2 hours and a half for 8 weeks, (first and last session: 3 hours) and an optional day of intensive practice of 6 hours, supervised by an MBSR instructor.
In each weekly session, the instructor creates a supportive environment in which:
* Guided meditation practices;
* Mindfulness stretching and yoga;
* Reflection and group discussion periods aimed at promoting mindfulness in daily life;
* Practice instructions and opportunity to ask questions;
* Instructions for home practice. Audio recordings and a manual are provided to support personal practice.
Audio recordings and a manual are provided to support personal practice
Standard group
No intervention in this group which will be followed according to the standard care
No interventions assigned to this group
Interventions
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MBSR (Mindfulness-Based Stress Reduction)
MBSR (Mindfulness-Based Stress reduction) program : 1 weekly session of 2 hours and a half for 8 weeks, (first and last session: 3 hours) and an optional day of intensive practice of 6 hours, supervised by an MBSR instructor.
In each weekly session, the instructor creates a supportive environment in which:
* Guided meditation practices;
* Mindfulness stretching and yoga;
* Reflection and group discussion periods aimed at promoting mindfulness in daily life;
* Practice instructions and opportunity to ask questions;
* Instructions for home practice. Audio recordings and a manual are provided to support personal practice.
Audio recordings and a manual are provided to support personal practice
Eligibility Criteria
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Inclusion Criteria
* With health insurance coverage
* Significant pruritus defined by a Visual Analogical Scale (VAS) pruritus ≥ 4
* Patient with plaque psoriasis
* Without joint involvement
* Mild to moderate severity (PASI\>10)
* DLQI \> 10
OR Patient with atopic dermatitis:
* Mild to moderate severity (SCORAD\>10)
* DLQI \> 10
* Diagnosis according to Hanifin and Raijka criteria
* Patient in a stable psychological state
* French langage spoken
Exclusion Criteria
* Psychiatric illnesses diagnosed according to the DSM-5 or ICD-10 international criteria of psychotic disorder, severe anxiety disorder, depressive disorder with a current depressive episode of severe intensity, bipolar disorder with a current depressive or manic episode
* Taking psychotropic or neuroleptic treatments
* Participation in another interventional research study or being in the exclusion period at the end of a previous study, if applicable
* Patient under AME
18 Days
ALL
No
Sponsors
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Assistance Publique - Hôpitaux de Paris
OTHER
Responsible Party
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Locations
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Hôpital Saint-Louis
Paris, , France
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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APHP211191
Identifier Type: -
Identifier Source: org_study_id
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