The Effectiveness of Virtual Reality on Anxiety Reduction in Women Undergoing Elective Egg Cryopreservation. (VRFORANXIETY)

Hadassah Medical Center

Status: Enrolling

Conditions: Anxiety

Treatments: Device: The VR instrument - Oculus Quest 2

Study type: Interventional

Funder types: Other

Identifiers

NCT06280222

VR FOR ANXIETY-HMO-CTIL

Details and patient eligibility

About

A randomized trial assessing the effectiveness of virtual reality exposure prior to an oocyte retrieval procedure in terms of anxiety level .

Full description

Eligible women, undergoing elective egg freezing, will be offered to participate in the study, and sign a consent form.

The patients will be randomized into 2 groups:

1. No intervention (routine management).
2. Exposure to scenery video, as a VR (virtual reality) session.

All women will be addressed prior to the procedure, while they are waiting, and upon consent will be asked to state their VAS (visual analogue scale) anxiety score and to fill the STAI (The State-Trait Anxiety Inventory questionnaire.) Vital signs (Heart rate, Blood pressure) will be recorded upon arrival.

Patients who were allocated to the VR arm will watch a 20-minute scenery video and following the session before entering the procedure will be asked to rate their VAS score and answer the STAI questionnaire once again. vital signs will be recorded again.

After recovery all women will fill the STAI questionnaire, VAS score and vital signs before they will be discharged.

Enrollment: 30 estimated patients

Sex: Female

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Patients before egg retrieval for social reasons (elective egg freezing)

Exclusion criteria

• Use of any medications for pain relief/ anti -anxiety /anti -depressants medication generally or prior to the intervention

• If suffers from any condition that Use of VR is not recommended:

  1. Risk for seizures
  2. Sensitivity to flashing light/motion
  3. Predisposing to nausea/dizziness (vertigo, etc.) Any injury to the eyes/face/neck that would limit the use of the hardware, including blindness.

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

---

30 participants in 2 patient groups

Routine management

No Intervention group

Description:

Usual care of patients prior to a surgical procedure : oocyte retrieval

Virtual reality management

Experimental group

Description:

20 minutes of scenery VR movies prior to the surgical procedure (oocyte retrieval)

Treatment:

Device: The VR instrument - Oculus Quest 2