Interest of Hypnosis on Pain Management During a Guided Echo Infiltration of the Hand

Study Results

Results available

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

80 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-10-08

Study Completion Date

2022-09-02

Brief Summary

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Ultrasound-guided infiltration is a common procedure and is known to be locally painful. This care-induced pain leads to strong apprehension in patients who need to benefit from this procedure.

The practice of hypnosis to improve the patient's comfort during a treatment has appeared progressively in hospital departments.

Among the various existing conversational hypnosis techniques, there is the "magic glove" technique. This is the technique that will be used in this study.

The investigators wish to evaluate the interest of hypnosis on the pain felt by the patient when performing an echo-guided infiltration of the hand, one of the most painful extremities during infiltrations.

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Detailed Description

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Conditions

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Hand Injuries

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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Infiltration

Ultrasound-guided hand infiltration

Group Type ACTIVE_COMPARATOR

Infiltration

Intervention Type PROCEDURE

Ultrasound-guided hand infiltration

Hypnosis

Hypnosis before Ultrasound-guided hand infiltration

Group Type EXPERIMENTAL

Hypnosis

Intervention Type PROCEDURE

conversational hypnosis technique call the "magic glove"

Infiltration

Intervention Type PROCEDURE

Ultrasound-guided hand infiltration

Interventions

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Hypnosis

conversational hypnosis technique call the "magic glove"

Intervention Type PROCEDURE

Infiltration

Ultrasound-guided hand infiltration

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Patient with an indication of a first hand infiltration under ultrasound examination
* Major patient
* Patient with capacity to understand the protocol and has given oral consent to participate in the research,
* Patient with social security coverage.

Exclusion Criteria

* Patient having preventively applied a pain patch to the area to be infiltrated
* Contraindication to infiltrations ( imbalanced diabetes, imbalanced,hypertension, ongoing infections).
* Hearing impaired patient
* Patient under guardianship/curtel
* Minor
* Pregnant woman
* Patient participating in another intervention research protocol
* Patient unable to follow the protocol as judged by the investigator.

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No