Assessment of Energetic Resonance by Cutaneous Stimulation on Withdrawal Alcohol Symptoms.
Not Applicable
Completed
- Conditions
- Alcohol Withdrawal Syndrome
- Registration Number
- NCT02146716
- Lead Sponsor
- Hospices Civils de Lyon
- Brief Summary
The purpose of RESC study is to assess the efficacy of Energetic Resonance by Cutaneous Stimulation on alcohol withdrawal symptoms measured by CUSHMAN score and in a second time to measure the benzodiazepine amount prescribed during the withdrawal time.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 43
Inclusion Criteria
- Men and women between 18 and 80 years,
- Patient with alcohol addiction,
- Patient needing alcohol withdrawal in a hospital.
- Patient with social Security,
- Patient with inform consent signed.
Exclusion Criteria
- Pregnant women
- Minor.
- Major with guardianship.
- People without sufficient information because of troubles of cognitive functions, or without sufficient knowledge of French language.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Cushman Score measure after Energetic Resonance by Cutaneous Stimulation daily during one week CUSHMAN score is represented by a scale with 7 variables collecting physiological modifications or behavioural manifestations related to adrenergic answer, neurovegetative signs, confusion, nervousness, perceptive or hallucinatory phenomena.
- Secondary Outcome Measures
Name Time Method Quality of life scale day 0 Anxiety depression scale pre-screening, day 3 and day 7 Analogic Visual Scale before and after each Energetic Resonance by Cutaneous Stimulationsession at day 2, day 4 and day 6. prescribed benzodiazepine amount day 0 to day 7
Trial Locations
- Locations (1)
Hôpital croix rousse
🇫🇷Lyon, France
Hôpital croix rousse🇫🇷Lyon, France