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Can Virtual Reality Technology Improve the Patient Experience in Oocyte Retrieval?

P

Peter Humaidan

Status

Enrolling

Conditions

Infertility, Female

Treatments

Device: Virtual reality technology

Study type

Interventional

Funder types

Other

Identifiers

NCT05826938
Virtual Reality-project

Details and patient eligibility

About

A non-pharmacological, non-blinded, randomized cohort study that will investigate the effect of Virtual Reality technology on the patient experience during oocyte retrieval.

The primary objective of the trial is to investigate the impact of Virtual Reality technology on the patient experience

Enrollment

82 estimated patients

Sex

Female

Ages

18 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Women undergoing oocyte retrieval
  • Understanding and speaking Danish

Exclusion criteria

  • Previous participation in the trial
  • Acupuncture as pain relief during oocyte retrieval

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

82 participants in 2 patient groups

Virtual reality
Experimental group
Description:
The intervention group receives stimuli in the form of Virtual Reality technology before and during oocyte retrieval. In addition, patients receive standard treatment
Treatment:
Device: Virtual reality technology
Control
No Intervention group
Description:
The control group, does not receive stimuli in the form of Virtual Reality technology, but only the standard treatment

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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