Hypnosis and smell therapy join forces to fight alcohol withdrawal anxiety
NCT ID NCT07444255
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a new way to help people going through alcohol withdrawal feel less anxious. It combines hypnosis with aromatherapy, using a calming scent to trigger the relaxation learned during hypnosis. About 80 adults in a hospital addiction unit will either get this combined treatment or standard care. The goal is to see if this approach reduces anxiety more than usual care alone.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 80 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Mar 2026
An estimate. Start dates often move.
- Expected to finish
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May 2029
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Hôpitaux Universitaires de Strasbourg
Strasbourg, France
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