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Virtual Reality for Pain and Anxiety Distraction Strategy on Office Hysteroscopy

Effectiveness of Virtual Reality as a Pain and Anxiety Distraction Strategy on Office Hysteroscopy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04721587
Acronym
VRPAD
Enrollment
160
Registered
2021-01-22
Start date
2020-02-18
Completion date
2023-06-30
Last updated
2023-12-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety, Pain, Acute

Keywords

Hysteroscopy, Pain, Virtual Reality, Anxiety

Brief summary

Hysteroscopy is a minimally invasive endoscopic technique that allows direct visualization of the uterine cavity and constitutes the gold standard for the diagnosis and treatment of most intrauterine pathology, such as heavy menstrual bleeding, fibroids, endometrial polyps, uterine malformations, etc. The see and treat strategy allows diagnosis and treatment in the same surgical act, and gives the technique a high resolution capacity, reducing the number of procedures the patient must undergo. The technological development of instruments has made it possible to have small-caliber endoscopic systems that have made this technique possible in an outpatient setting. Outpatient management allows patients to avoid the possible risks and inconveniences associated with the surgical environment, such as the waiting list and the need for anesthesia, as well as an earlier return to their activities of daily life. Despite the high resolution rates, a not inconsiderable percentage of women experience anxiety or pain during outpatient hysteroscopy, and this is the leading cause of treatment failure. In order to improve the tolerance and comfort of the patient, the usefulness of various strategies, both pharmacological and non-pharmacological, has been evaluated for pain reduction, with different results. Virtual Reality (VR) has been used successfully to reduce perceived pain in various procedures such as chronic pain, burns, dental processes, chronic pruritus or venipuncture. There is no published study to our knowledge that evaluates the usefulness of VR in reducing the levels of anxiety and pain perceived during a hysteroscopic procedure. The working hypothesis to be evaluated with this study is that the use of a VR device with reproduction of relaxing and distraction environments reduces the perception of pain and anxiety of the patient during an outpatient hysteroscopy.

Interventions

DEVICEVirtual Reality

The patients of the VR Group will be subjected to the same hysteroscopy technique as the Standard of Care Group, but additionally a VR device will be applied where a distraction VR environment (Underwater Game) will be reproduced during the exploration

Sponsors

Psious
CollaboratorUNKNOWN
Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Being over 18 years * Understand and accept the study procedures * Sign the informed consent. * Indication of outpatient hysteroscopy according to the care protocols of the center * Not taking drugs for the treatment of anxiety.

Exclusion criteria

* Not being able to understand the nature of the study and / or the procedures to be followed * Not signing the informed consent * Be under the age of 18 * Pregnancy * Being diagnosed with anxiety disorder or being treated with anxiolytics * Patients suffering from vertigo * Patients with epilepsy * Active ear infection * Patients with diagnosed hypertension * Patients with cardiovascular disease * Patients with psychosis or severe mental illness

Design outcomes

Primary

MeasureTime frameDescription
Pain scoreIntraprocedureDecrease of 1 point or more in the level of pain measured by an 11-point visual analog scale, a validity scale that comprises 11 consecutive values from 0 to 10, with 0 corresponding to no pain and 10 to worst pain imaginable.

Secondary

MeasureTime frameDescription
Heart RateIntraprocedureChanges in basal Heart Rate, maximum Heart Rate, mean Heart Rate, and final Heart Rate.
Blood PressureIntraprocedureChanges in pre and postprocedure blood pressure
Skin conductaceIntraprocedureChange between basal and maximum skin conductance levels during pocedure measured by a small sensor placed on two hand fingers. Skin conductance depends directly on the state of relaxation or stress, making it a commonly used and very precise stress indicator.

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026