Hypnosis und Progressive Musclerelaxation for stressreduction for mild depression– a prospective, randomized, controlled, exploratory telemedicine pilot study
- Conditions
- F32.0Mild depressive episode
- Registration Number
- DRKS00032115
- Lead Sponsor
- Charité - Universitätsmedizin Berlin Institut für Sozialmedizin, Epidemiologie und Gesundheitsokönomie
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 60
Women, men, and individuals of diverse genders between the ages of 18 and 70.
-Subjective stress level in the past week on the Visual Analog Scale (VAS) 40 mm (VAS 0 - 100 mm, 0 = no stress and 100 = maximum imaginable stress).
-Diagnosis of mild depression according to ICD-10 (F32.0, F33.0) by a specialist in psychiatry and psychotherapy or a licensed psychological psychotherapist.
-Duration of depressive symptoms for at least 2 weeks.
-Capacity to provide informed consent and signed informed consent form.
-Technical equipment to participate in online courses and complete online questionnaires.
-Known history of severe trauma resulting in post-traumatic stress disorder.
-Diagnosed personality disorder.
-Current or past psychotic disorder
-Acute self-harm or suicidality
-Known severe obsessive-compulsive disorder.
-Alcohol and drug dependency.
-Presence of moderate or severe acute or chronic physical illness. -Participation in another study on depression within the last 2 months prior to study enrollment.
-Lack of understanding of the German language.
-Ongoing disability retirement process.
-Use of hypnosis, self-hypnosis, autogenic training, or progressive muscle relaxation (PMR) currently or within the last 2 months.
-Diagnosis of moderate and severe depressive episode according to ICD-10 (F32.1, F32.2, F33.1, F33.2) by a specialist in psychiatry and psychotherapy or a licensed psychological psychotherapist.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method