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Clinical Trials/NCT02528578
NCT02528578
Completed
N/A

Modulation of Painful Perception

Centre Hospitalier Universitaire de Saint Etienne2 sites in 1 country74 target enrollmentJune 2013
ConditionsHealthy

Overview

Phase
N/A
Intervention
Not specified
Conditions
Healthy
Sponsor
Centre Hospitalier Universitaire de Saint Etienne
Enrollment
74
Locations
2
Primary Endpoint
Intensity of the perceived pain assessed by the volunteer by a analog scale (VAS) at each thermal stimulation.
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

The objective of the study is to evaluate in healthy volunteers, the influence of empathy on pain perception.

It is widely accepted in the clinical management that the feeling of listening to the patients' pain would have a favorable influence on the pain, and conversely, the lack of listening would be aggravating.

In this study, the volunteer will receive painful thermal stimuli in empathetic context (l, empathetic or non-empathetic) Two situations will oppose, one where the examiner neglect or minimize the suffering of the voluntary and the other or the contrary, the subject will receive empathy.

The first part of the project is to verify that the pain is influenced by the empathetic context. The second part will be conducted functional MRI, which should isolate the brain regions affected by other people's empathy for pain.

Registry
clinicaltrials.gov
Start Date
June 2013
End Date
November 2015
Last Updated
8 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Right handed

Exclusion Criteria

  • Pregnant or lactating women,
  • Against-indications to MRI
  • Drug intake of less than 12 hours,
  • Neurological history or deficits, psychiatric, auditory or visual.
  • Decline to participate

Outcomes

Primary Outcomes

Intensity of the perceived pain assessed by the volunteer by a analog scale (VAS) at each thermal stimulation.

Time Frame: Day 0

Secondary Outcomes

  • blood-oxygen-level dependent (MRI)(Day 0)

Study Sites (2)

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