Cognitive Trance, Hypnosis and Meditation in Oncology
Cancer, Distress, Emotional, Pain
About this trial
This is an interventional supportive care trial for Cancer focused on measuring Hypnosis, Cognitive trance, Meditation, Cancer, Oncology, Quality of life, Neurophysiology, Phenomenology
Eligibility Criteria
Inclusion Criteria:
- ≥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.
Exclusion Criteria:
- < 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
Sites / Locations
- University of LiègeRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Experimental
Experimental
Experimental
No Intervention
Hypnosis
Cognitive trance
Meditation
Control group
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.
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.
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.
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.