Comparison of the Effect on Anxiety of Combining Hypnosis and Aromatherapy Through Olfactory Anchoring Versus Standard Care in Patients Undergoing Alcohol Withdrawal
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Usual treatment, Experimental treatment.
- Who it may be relevant to
- Registry conditions: Alcohol Withdrawal, Anxiety. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- France
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Randomized Trial Comparing the Effect on Anxiety of Combining Hypnosis and Aromatherapy Through Olfactory Anchoring Versus Standard Care in Patients Undergoing Alcohol Withdrawal
Overview
According to a meta-analysis published in 2019, hypnosis has demonstrated positive effects in the treatment of certain mental illnesses, particularly anxiety. This technique aims to put the subject into a particular state of consciousness conducive to therapeutic action. The safe place in hypnosis is the basis for anxiety relief work, the first step towards the use of hypnotic metaphors. Smell is an excellent way to stimulate the imagination in creating this safe place. Anchoring allows the effects of a hypnosis session to be reactivated, enabling the subject to re-experience its benefits through tactile stimulation, a key word, or an image. The investigators use olfactory stimulation as a hypnotic anchor while also utilizing the anxiolytic properties of essential oils. While there are already studies on the use of hypnosis or aromatherapy in the treatment of patients who use psychotropic drugs, no study to date has focused on their combined use. The innovative aspect of this treatment lies in the prolongation and reinforcement of the effect of the hypnosis session through olfactory stimulation. The literature shows that memories triggered by a smell have the ability to materialize physiologically in the areas of the brain that process spatial and temporal information. This is also a goal that hypnosis aspires to achieve. The investigators hypothesize that the use of these two tools in formalized, time-limited nursing interviews can provide patients in the complex withdrawal unit with the means to reduce their anxiety in the short and medium term.
Interventions
- Other Usual treatment
Withdrawal care provided according to standard practice - Other Experimental treatment
Treatment for withdrawal using hypnosis and aromatherapy
Primary outcome measures
- Change of anxiety disorders as assessed by the Hamilton Anxiety Scale between the start and end of the patient's hospitalization. [Time frame: Day 0 and Day 15]
Eligibility criteria
Inclusion criteria
- Patients aged 18 or over
- Patients hospitalized in an addiction unit for acute alcohol withdrawal and suffering from anxiety disorders
- Patients affiliated with a social security health insurance scheme, beneficiaries or dependents
- Patients who speak/read French, are able to understand the objectives and risks associated with the research, and can give dated and signed informed consent
- Patients who adhere to complementary therapies
- For women of childbearing age, patients for whom the beta HCG test (urine or blood, performed routinely) is negative and who are using effective contraception.
Exclusion criteria
- Allergy(ies)/contraindication(s) to essential oils selected for the project
- Patients with psychosis or complex psychological trauma
- Anosmia, hyposmia, or other olfactory disorders limiting the quality of smell
- Asthma
- Ear, nose and throat pathology(ies) contraindicating essential oils in olfaction
- Skepticism regarding the effectiveness of hypnosis and aromatherapy
- Patient under guardianship/curatorship
- Patients excluded from a previous or ongoing study
- Patients in an emergency or life-threatening situation
- Patients under legal guardianship
- Patients who have already participated in this study
- Pregnancy
- Breastfeeding
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Treatment
Study locations
France · 1 center
- Hôpitaux Universitaires de Strasbourg — Strasbourg
Identifiers
NCT: NCT07444255 · RC25-0040