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临床试验/NCT07444255
NCT07444255尚未招募不适用

Randomized Trial Comparing the Effect on Anxiety of Combining Hypnosis and Aromatherapy Through Olfactory Anchoring Versus Standard Care in Patients Undergoing Alcohol Withdrawal

University Hospital, Strasbourg, France1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2026年3月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
80
试验地点
1
主要终点
Change of anxiety disorders as assessed by the Hamilton Anxiety Scale between the start and end of the patient's hospitalization.

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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.

排除标准

  • 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
  • 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

研究组 & 干预措施

Patients Undergoing Alcohol Withdrawal treated by usual treatment

Active Comparator

干预措施: Usual treatment (Other)

Patients Undergoing Alcohol Withdrawal treated with Hypnosis and Aromatherapy

Experimental

干预措施: Experimental treatment (Other)

结局指标

主要结局

Change of anxiety disorders as assessed by the Hamilton Anxiety Scale between the start and end of the patient's hospitalization.

时间窗: Day 0 and Day 15

次要结局

未报告次要终点

研究者

发起方
University Hospital, Strasbourg, France
申办方类型
Other
责任方
Sponsor

研究点 (1)

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