Meditation in Inflammatory Dermatosis

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorAssistance Publique - Hôpitaux de Paris

About this trial

Psoriasis and atopic dermatitis are multifactorial inflammatory dermatoses, with a very high prevalence, reaching more than 120 million patients in the world. Although the physiopathological mechanisms are not yet clearly defined, these inflammatory dermatoses involve an interaction between the immune system and the epidermal cells, severe skin inflammation and often very intense pruritus. The objectives of an effective management should be to treat lesions in order to reduce them, but also to reduce itching and allow the patients to accept and cope with their pathology, without neglecting an improvement in the "Dermatology Life Quality Index" (DLQI) and in the psychological state, sometimes depressive, of the patient. Itching is defined as "a feeling that needs to be scratched urgently" and can cause significant distress along with pain. It severely impacts the quality of life and the quality of sleep. Chronic itching is associated with increased stress, anxiety, and other mood disorders. In turn, stress and anxiety exacerbate the itching, leading to a vicious cycle of pruritus - scratching that affects patient behavior (excessive scratching) and worsens disease prognosis and quality of life. Much research over the past few decades has demonstrated the effect of mindfulness meditation on emotional and cognitive responsiveness, cognitive flexibility, rumination, self-compassion and mindfulness, but also on acute pain, anxiety, stress, depression, cardiovascular disease, eating disorders, cancer and cognitive loss with age. Several studies have shown the impact of mindfulness on brain function and immunity, with evidence for the association between mindfulness and changes in the levels of markers characteristic of immune system activity and inflammation, known to be increased in psoriasis or atopic dermatitis. The objective is to evaluate the effect of mental training in the regulation of stress and emotions through mindfulness meditation in patients with moderate, itchy atopic dermatitis or psoriasis, not treated with systemic agents (e.g.: biotherapies). This project is based on the premise that mental training in the regulation of stress and emotions through meditation would reduce the effects of the infernal itch-scratch cycle, alleviating pruritus, thus improving the well-being and mental health of patients while reducing their inflammatory skin lesions and limiting the appearance of new lesions.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patient aged 18 years old or older

With health insurance coverage

Significant pruritus defined by a Visual Analogical Scale (VAS) pruritus ≥ 4

Patient with plaque psoriasis

Disqualifiers

Current systemic treatment or treatment discontinued within the last month

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

Trial design

Design model

Parallel

Treatments tested in this trial

  • MBSR (Mindfulness-Based Stress Reduction)

    Other intervention

    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

Treatment groups

72 Participants
are divided into 2 treatment groups
Group A: MBSR (Mindfulness-Based Stress Reduction) groupExperimental treatment 1 intervention
Group B: Standard groupNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Pruritus assessed by Visual Analogue Scale (VAS)

VAS Pruritus scale is a scale going from 0 to 10. 0 corresponds to no pruritus et 10 to the maximum of prurit.

Time frame
at 8 weeks

Secondary outcomes

1

Pruritus assessed by Visual Analogue Scale (VAS)

VAS Pruritus scale is a scale going from 0 to 10. 0 corresponds to no pruritus et 10 to the maximum of prurit.

Time frame
at 16 weeks
2

Pruritus assessed by 5-D Itch Scale 5-D (5-D IQ)

The 5-D itch scale is a multidimensional questionnaire. The scores of each of the domains are achieved separately and then summed together : total 5-D score can potentially range between 5 (no pruritus) and 25 (most severe pruritus).

Time frame
at 8 weeks
3

Pruritus assessed by 5-D Itch Scale 5-D (5-D IQ)

The 5-D itch scale is a multidimensional questionnaire. The scores of each of the domains are achieved separately and then summed together : total 5-D score can potentially range between 5 (no pruritus) and 25 (most severe pruritus).

Time frame
at 16 weeks as compared to 8 weeks
4

Number of dermatocorticoides tubes

Time frame
at 8 weeks

Other outcomes

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