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临床试验/NCT04873661
NCT04873661进行中(未招募)不适用

Hypnosis, Meditation and Cognitive Trance on Cancer Patients: Impact on Quality of Life and Neurophysiology

University of Liege1 个研究点 分布在 1 个国家目标入组 160 人开始时间: 2021年1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
进行中(未招募)
入组人数
160
试验地点
1
主要终点
Change in Emotional distress

研究概览

简要总结

Patients with cancer often suffer from a symptom cluster, including pain, fatigue, sleep difficulties, emotional distress and cognitive impairments. In oncology settings, there is a growing interest in "mind-body" intervention, to relieve them in a non-pharmacological way. Hypnosis and meditation are two modified state of consciousness shown to positively this symptom cluster. Cognitive trance is also a modified state of consciousness, but is induced by body movements and/or vocalizations. Subjective reports of experts in cognitive trance showed a modification of self, emotion regulation, pain perception, attention and concentration. However, we still need to develop studies to better characterise this particular state of consciousness and its clinical applications. Our randomized-controlled trial aims at comparing both interventions in terms of (1) benefits on cancer patients' quality of life (pain, fatigue, sleep, distress, cognitive impairments), (2) phenomenological/subjective experiences and neurophysiological correlates, and (3) mechanisms involved in patients' responsiveness, based on the biopsychosocial model of hypnosis.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Supportive Care
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
否

入选标准

  • •≥18 years old
  • •No neurological/psychiatric disorders/history of alcohol or drug abuse
  • •No current and regular practice of hypnosis, meditation or cognitive trance
  • •Diagnosis of cancer (all localisations accepted except brain tumours to avoid any effect on EEG data and cognitive impairments)
  • •Active treatments (surgery, chemotherapy, radiotherapy) finished for less than a year.
  • •Score of at least 4/10 for one of these four symptoms at baseline: pain, fatigue, sleep difficulties, emotional distress.

排除标准

  • •< 18 year old
  • •No cancer diagnosis
  • •Neurological or psychiatric disorder
  • •Brain tumour ou other tumour with brain metastases
  • •Active treatments still ongoing or finished for more than a year
  • •No baseline symptom at 4/10

研究组 & 干预措施

Hypnosis

Experimental

In the hypnosis-based intervention, patients (in groups of approximately 10 participants) will participate in 8 weekly sessions (2 hours each) during which they will benefit from guided hypnosis exercises, and learn how to implement self-hypnosis. They will also receive a CD with hypnosis exercises for home practice. At-home practice is encouraged between sessions.

干预措施: Hypnosis group intervention (Behavioral)

Cognitive trance

Experimental

The cognitive trance-based intervention will consist of a two-day workshop in groups of approximately 10 participants, where they will learn how to induce the cognitive trance, with the use of different sound-loops that can induce trance in untrained people in a safe way. After two weeks of home practice, participants will redo a two-day consolidation training. At-home practice is encouraged between sessions.

干预措施: Cognitive trance group intervention (Behavioral)

Meditation

Experimental

The meditation-based intervention will consist of 8 weekly sessions (2h45 each) in groups of approximately 10 participants, as well as half a day of intensive practice between the fifth and the sixth session. Participants will learn how to implement self-compassion meditation, through practical exercises proposed during the sessions. At-home practice is encouraged between sessions.

干预措施: Meditation group intervention (Behavioral)

Control group

No Intervention

Participants in the control group will not receive any intervention during the whole duration of the study. They will be assessed at the same times and in the same ways than the 3 experimental groups. After the study, they will have the opportunity to participe in one of the 3 interventions if they want to.

结局指标

主要结局

Change in Emotional distress

时间窗: Assessed before the intervention (T0), immediately after the intervention (T1), and at 3- and 12-month follow-up (T3 and T4)

Assessed with a questionnaire (Hospital Anxiety and Depression Scale; HADS). Score range from 0 to 42, with a higher score indicating higher emotional distress

Change in Fatigue

时间窗: Assessed before the intervention (T0), immediately after the intervention (T1), and at 3- and 12-month follow-up (T3 and T4)

Assessed with a questionnaire (Multidimensional Fatigue Inventory; MFI-20)

Change in Pain

时间窗: Assessed before the intervention (T0), immediately after the intervention (T1), and at 3- and 12-month follow-up (T3 and T4)

Assessed with a visual analogue scale (VAS) (score range from 0 to 10/10, a higher score indicating a higher pain)

Change in Sleep difficulties

时间窗: Assessed before the intervention (T0), immediately after the intervention (T1), and at 3- and 12-month follow-up (T3 and T4)

Assessed with a questionnaire (Insomnia Severity Index; ISI). Score range from 0 to 28, with a higher score indicating higher sleep difficulties.

Change in Perceived cognitive difficulties

时间窗: Assessed before the intervention (T0), immediately after the intervention (T1), and at 3- and 12-month follow-up (T3 and T4)

Assessed with a questionnaire (FACT-Cog), investigation 4 dimensions (perceived cognitive impairments, score range 0-72, higher score indicating less impairments ; impact of cognitive impairments on quality of life, score range 0-16, with higher scoe indicating less impact ; Comments from others, score range 0-16 with higher score indicating less comments ; perceived cognitive abilities, score range 0-28, with higher score indicating more cognitive abilities)

次要结局

  • Change in the quality of the relationship with the therapist who animated the group sessions(Assessed immediately after the intervention (T1), and at 3- and 12-month follow-up (T3 and T4))
  • Change in body temperature(Resting state : Assessed before the intervention (T0), immediately after the intervention (T1), and at 12-month follow-up (T4). During hypnosis, trance or meditation : T1, T4.)
  • Fantasy Proneness (imaginative experiences)(Assessed before the intervention (T0))
  • Change in Empowerment(Assessed before the intervention (T0), immediately after the intervention (T1), and at 3- and 12-month follow-up (T3 and T4))
  • Change in Characteristics of the intense memory described above(Assessed immediately after the intervention (T1), and at 3- and 12-month follow-up (T3 and T4))
  • Change in body movements(Resting state : Assessed before the intervention (T0), immediately after the intervention (T1), and at 12-month follow-up (T4). During hypnosis, trance or meditation : T1, T4.)
  • Change in Psychological flexibility(Assessed before the intervention (T0), immediately after the intervention (T1), and at 3- and 12-month follow-up (T3 and T4))
  • Personnality characteristics(Assessed before the intervention (T0))
  • Expectations and motivation to participate in the chosen intervention(Assessed before the intervention (T0))
  • Change in the characteristics of a free recall of an intense hypnosis/cognitive trance/meditation episode (or an intense autobiographical episode for the participants in the control group)(Assessed immediately after the intervention (T1), and at 3- and 12-month follow-up (T3 and T4))
  • Change in presence during the intense memory described above(Assessed immediately after the intervention (T1), and at 3- and 12-month follow-up (T3 and T4))
  • Change in Emotion regulation(Assessed before the intervention (T0), immediately after the intervention (T1), and at 3- and 12-month follow-up (T3 and T4))
  • Change in Mystical characteristics of the intense memory described above(Assessed immediately after the intervention (T1), and at 3- and 12-month follow-up (T3 and T4))
  • Change in Mental Adjustment to Cancer(Assessed before the intervention (T0), immediately after the intervention (T1), and at 3- and 12-month follow-up (T3 and T4))
  • Personal definition of hypnosis/cognitive trance/meditation(Assessed before the intervention (T0))
  • Change in cerebral activity(Resting state : Assessed before the intervention (T0), immediately after the intervention (T1), and at 12-month follow-up (T4). During hypnosis, trance or meditation : T1, T4.)
  • Change in heart rate(Resting state : Assessed before the intervention (T0), immediately after the intervention (T1), and at 12-month follow-up (T4). During hypnosis, trance or meditation : T1, T4.)
  • Change in respiration(Resting state : Assessed before the intervention (T0), immediately after the intervention (T1), and at 12-month follow-up (T4). During hypnosis, trance or meditation : T1, T4.)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Audrey Vanhaudenhuyse

PhD in Medical Sciences

University of Liege

研究点 (1)

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