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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05036772
Other study ID # Daphné
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 30, 2022
Est. completion date March 8, 2024

Study information

Verified date March 2024
Source Poitiers University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Compare the maximum pain and anxiety experienced between the group using a virtual reality headset and the control group in an adult woman during a hysterosalpingography examination


Description:

In France, 1 couples out of 5 consults for suspected infertility. Hysterosalpingography is the first line diagnostic examination in this course and can sometimes be therapeutic. This gynecological examination is invasive in nature, this exam requires an administration of iodinated contrast product by the endocavitary route. Hysterosalpingography is the most painful examination in this treatment path and pain's assessment is classified as strong by the French National Authority for Health (Haute Autérité de Santé) and anxiety-inducing. For these patients, drug analgesic treatments remain ineffective or contraindicated in outpatient mode. Ionizing irradiation is a constraint that makes hypnosis unsuitable. Several studies show the contribution of a virtual reality headset in reducing pain and anxiety by inducing patients in an hypnotic environment. This tool standardizes interventions based on changes in consciousness. It is an easy-to-use, non-drug analgesia with few side effects and inexpensive. The environment offered by this medical device is based on evidence to peacefully escort patients on a journey of natural elements. Calm music is made up of key elements of musical therapy. A medical anesthesiologist and hypnotherapist wrote the hypnotic induction. And, the voice is the one of an experienced sociologist in practice. A simple meditation modeled on heart synchronization sets a persistent goal during this immersion.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date March 8, 2024
Est. primary completion date March 8, 2024
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - patients over 18 years old - patients with a prescription for hysterosalpingography - patients able to answer the questionnaire independently (French-speaking or understanding French) - informed consent, signed by the patient - patients benefiting from a social security scheme or benefiting through a third party Exclusion Criteria: - patients with a contraindication to virtual reality headset. - refusal to participate in the study - Contraindication to the realization of hysterosalpingography (pregnancy / lactation or infection) - patient under guardianship, curatorship or subordination

Study Design


Intervention

Device:
Virtual reality
The experimental arm will have the possibility to use a distracting virutel environment for the duration of hysterosalpingography.

Locations

Country Name City State
France Centre Hospitalier Universitaire Poitiers

Sponsors (1)

Lead Sponsor Collaborator
Poitiers University Hospital

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary visual analog scale (EVA) The patient rates her pain level between 0 and 10. The standard question is: "From 0 to 10, with 0 absence of pain and 10 maximum pain, how much will you rate the maximum pain experienced during your examination?" through study completion, an average of 1 year
Secondary anxiety assessment State Trait Inventory Anxiety (STAI Y-A) anxiety assessment questionnaire through study completion, an average of 1 year
Secondary Dosimetry Collection of the dose report produced surface in mGy.cm² through study completion, an average of 1 year
Secondary Time of exam Measurement of the time in minutes between the first shot and the last shot (the late evacuation shot will not be taken into account) through study completion, an average of 1 year
Secondary - Cybersickness evaluation simplified Virtual Reality Sickness Questionnaire (VRSQ) cybersickness scale. (Questionnaire in 9 items) through study completion, an average of 1 year
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