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Changes in Perception and Cognition During a Meditation Retreat (LONGIMED)

Civil Hospices of Lyon logo

Civil Hospices of Lyon

Status

Completed

Conditions

Healthy Volunteers

Treatments

Behavioral: 10 days intensive meditation retreat
Behavioral: Waiting for a 10 days intensive meditation retreat

Study type

Interventional

Funder types

Other

Identifiers

NCT04449913
69HCL20_0003
2020-A00669-30 (Other Identifier)

Details and patient eligibility

About

This study aims at assessing neuro-behavioral changes occuring during an intensive ten days meditation retreat. The investigator will study changes in tactile, auditory and pain perceptions as well as changes in cognitive and affective mental contents and their neural markers, as measured by self-reports, EEG event-related potentials, and functional connectivity of resting state fMRI. He will recruit healthy participants with a prior meditation experience. They will be randomly assigned to two groups, one active group who will undergo measurements just before, during and 3 weeks after the retreat. The other group will serve of control for task habituation, control participants will undergo the same measurements, equally spaced in time, but before the retreat. The main hypothesis is that meditation training strengthens meta-awareness, attention capacities resulting in enhanced bodily- and self-awareness during sensory perception and emotion regulation during pain.

Enrollment

58 patients

Sex

All

Ages

18 to 67 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age between 18 and 67
  • Regular meditation practice (at least 20 minutes 3 times a week) arising from a formal teaching (buddhist tradition, MBSR, mindfulness) for at least one year.
  • Having taken part to at least one intensive retreat (more than six hours of sitting meditation a day, during at least two days) in the past.
  • Affiliated to french social security
  • Motivated to take part in the study
  • Having signed an informed consent
  • Normal or corrected vision
  • Sufficient mastering of French to be able to understand correctly written and auditory instructions

Exclusion criteria

  • neurological or psychiatric antecedents
  • chronical pain or any other medical condition giving rise to acute pain or sensitivity to pain.
  • Motor or sensory deficit in the hands
  • severe auditory loss
  • regularly taking medical drugs acting on the central nervous system
  • regularly taking opioids or antidepressant drugs
  • alcohol consumption above the safety threshold recognized by the French healthy agency (10 drinks a week, 2 drinks a day, 5 drinks for special occasions)
  • drugs consumption (except tabacco) qualified as addictive according to medical criteria (https://www.drogues.gouv.fr/comprendre/l-essentiel-sur-les-addictions/qu-est-ce-qu-une-addiction)
  • alcohol or drug consumption the day before or the day of experiment and during the full duration of the retreat
  • being pregnant, breastfeading or having given birth less than 6 months ago
  • Will be excluded from the fMRI task only, participants presenting contraindication to a MRI scan : being claustrophobic, body mass index over 30, people, having a pacemaker or an insuline pump, metallic prothesis, intracranial clip, neurosensory stimulator, in-body defibrillator, cochlear implants, ocular or brain feromagnetic bodies close to nervous structures, neurosurgery stunts, dental brace.

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

58 participants in 2 patient groups

Active group
Experimental group
Description:
10 days intensive meditation retreat
Treatment:
Behavioral: 10 days intensive meditation retreat
Control group
Other group
Description:
Waiting for a 10 days intensive meditation retreat
Treatment:
Behavioral: Waiting for a 10 days intensive meditation retreat

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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