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CompletedNCT02971852Updated Jul 21, 2017

Effects of Hypnosis on Skin Temperature

An observational study in Hypnosis and Healthy Volunteers, sponsored by Claude Bernard University. Completed at 3 sites in France. Open to participants aged 18 Years to 75 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2017-07-21.

Sponsored by Claude Bernard University · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
30
Ages
18 Years to 75 Years
Sex
All
01

Study summary

Hypnotic glove anesthesia is a hypnosis technique wherein the patient, following the suggestions of the hypnotherapist, is mentally capable to create a loss of sensation in areas of the hand that would be covered by a glove. We investigated the effects of hypnotic glove anesthesia on skin temperature measured by thermography.

Read the detailed description

After 20 min installation and temperature equilibration (T0), the subject skin temperature was recorded in 5 regions of both hands (1 = distal hand, 2 = proximal hand, 3 = wrist, 4 = distal forearm, 5 = proximal forearm) using infrared thermography.

After 10 min of latency, skin temperature was recorded again in both hands (T1).

A first noxious stimulus (NOX1) is then applied by the hypnotherapist by pinching the webbing between the thumb and index fingers of the dominant hand between the thumb and the index. Pain intensity is assessed on a 0-10 (0 = no pain, 10 = maximal pain imaginable) numerical rating scale (NRS1).

The hypnotic glove is then mentally created by the subject on his dominant hand following the suggestions of the hypnotherapist (T2). To assess the efficacy of the hypnotic glove, a second noxious stimulus (NOX2) is applied similarly to NOX1 and the NRS was recorded (NRS2).

The subject is then invited to mentally wear off the glove (T3). Skin temperature is then recorded in both hands, and a third noxious stimulus (NOX3) is applied similarly to NOX1 and NOX2 to verify the disappearance of hypnotic anesthesia.

A last record of skin temperature in both hands is performed 5 min after the glove is withdrawn (T4).

02

Conditions studied

  • Hypnosis
  • Healthy Volunteers

Keywords

  • Hypnosis
  • Anesthesia
  • Suggestion
  • Thermography
03

In context

Lead sponsor

Claude Bernard University is the lead sponsor of 29 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Healthy volunteers

Inclusion criteria

  • Healthy volunteers aged from 18 to 75

Exclusion criteria

Exclusion Criteria:

  • Neurologic or psychiatric disorder
  • Upper limb amputation
  • Microcirculation abnormalities (e.g. Raynaud syndrome)
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
30 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Change in skin temperature during the experiment in the hand and forearm

    Comparison of skin temperature between the dominant ("wearing" the hypnotic glove) and the non-dominant hand and forearm in the 5 predefined regions from Time 0 to Time 4.

    Time frame: During the study experiment, from the beginning of the experiment, after 20 min installation and temperature equilibration, to the end of the experiment, 5 min after the glove is mentally withdrawn (approximately 1 h).

Secondary outcomes

  1. Change in pain intensity during the experiment following noxious stimulation

    Comparison of pain intensity following noxious stimulation assessed by 0-10 NRS scale at Time 1, Time 2 and Time 3 in the dominant hand ("wearing" the hypnotic glove).

    Time frame: During the study experiment, from 10 min after the beginning of the experiment to 5 min before the end of the experiment, when the glove is mentally withdrawn (approximately 45 min).

07

Study locations

3 sites
  • Institut Émergences
    Rennes, 35000, France
  • Centre hospitalier privé Saint-Grégoire
    Saint-Grégoire, 35768, France
  • Centre Clinical
    Soyaux, 16800, France
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 21, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02971852
Lead sponsor
Claude Bernard University
Collaborators
Centre Clinical, France, Saint-Gregoire Private Hospital Center, Institut Émergences, France
Responsible party
Emmanuel Boselli (MD, PhD, Claude Bernard University) — Principal investigator
First posted
Nov 23, 2016
Start date
Nov 2016
Primary completion
Mar 2017
Completion
Mar 2017
Last update
Jul 21, 2017

Study contacts

Xavier Paqueron, MD, PhD
principal investigator · Centre Clinical, France

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2017. You cannot join it, but the record below documents what was studied.

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