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Neural Correlates of Self

The Neural Correlates of the Self in Altered States of Consciousness

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03206840
Acronym
NeuCoSe
Enrollment
100
Registered
2017-07-02
Start date
2017-10-26
Completion date
2018-11-12
Last updated
2025-11-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy Volunteers

Keywords

mindfulness meditation, hypnosis, meta-awareness, absorption, consciousness, self

Brief summary

Despite the increasing popularity of mindfulness meditation and hypnosis in healthcare and in the general community the underlying neurobiological mechanisms are unclear. The change in the relationship between the self and the conscious experience that they bring about may be crucial. This study aims to identify the neural correlates of self-consciousness in meta-awareness and absorption - using functional Magnetic Resonance Imaging (fMRI) in healthy participants combined with detailed first-person experiential accounts and behavioural tasks. This study will provide important clues about the widely reported effects of mindfulness meditation and hypnosis and shed light on the neural correlates of the conscious experience of self.

Interventions

BEHAVIORALcontrol, meditation, hypnosis.

three instructions will be given to each participant: control, meditation, hypnosis. The order of meditation and hypnosis will be randomized amongst two groups to avoid order effects.

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* aged 18-70 * Body mass index between 18.5 and 30 * Covered by health insurance * motivated to participate * signed informed consent * normal or corrected-to-normal eyesight * sufficient command of French to be able to follow the instructions

Exclusion criteria

* history of neurological or psychiatric conditions * chronic pain or another medical condition altering pain perception * use of medication that affects the central nervous system * use of opioids or antidepressant medication * severe auditory loss * consumption of alcohol or intoxicants on the day of the experiments and the day preceding the experiments * pregnancy, breastfeeding or having given birth \<6months ago * any contra-indication to Magnetic Resonance Imaging (metal implants or foreign bodies), agitation, claustrophobia

Design outcomes

Primary

MeasureTime frameDescription
Reaction time (minutes)at day 1reaction times during behavioural tasks.
Brain activation with IRMAt day 3Activation of different brain areas, as measured with functional Magnetic Resonance

Secondary

MeasureTime frameDescription
personality trait with questionnairesat day 2scores on different personality questionnaires
Scores during behavioural tasksat day 1scores on likert scale (1-5 and 1-9) about intensity of the stimui presented during the task
salivary volume (millimeter)at day 1salivary volume after behavioural tasks

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026