Investigating the effect of Virtual Reality in intrauterine sperm inseminatio

Not Applicable

Recruiting

• Conditions: Condition 1: Adjustment disorders (occurrence of worry, anxiety and depression following a special and critical situation in life). Condition 2: Reaction to extreme stress, unspecified (commonly seen in infertility). Condition 3: Dangerously obsessive thoughts or ruminations (which prevents the infertile person from going to the hospital to receive further treatment and can lead to more dangerous results for the person).; Adjustment disorders; Reaction to severe stress, unspecified; Predominantly obsessional thoughts or ruminations; F43.2; F43.9; F42.0

• Registration Number: IRCT20231013059702N2
• Lead Sponsor: Oroumia University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 6 March 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 114

Inclusion Criteria

Consent to participate in the study
Not having children at home
The first treatment experience with sperm intrauterine insemination
Infertility of female origin
No physical illness
Not having mental disorders and no history of drug use in the mental and psychological field
No visual impairments
No hearing disorders
No movement disorders
No addiction to smoking, drugs and alcohol
The absence of stressful events in the last 6 months, such as the death of loved ones, accidents, etc

Exclusion Criteria

Infertility of male origin
A candidate for treating infertility with methods other than intrauterine sperm insemination

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Worry score in the Pennsylvania Worry Questionnaire. Timepoint: Measuring people's level of concern using a questionnaire one hour before the start of the sperm transfer process into the uterus and half an hour after the sperm transfer process into the uterus. Method of measurement: Pennsylvania Anxiety Inventory.;Hospital anxiety and depression score in Zigmond and Snaith hospital anxiety and depression questionnaire. Timepoint: Measuring the level of anxiety and depression of people using a questionnaire one hour before the start of the sperm transfer process into the uterus and half an hour after the sperm transfer process into the uterus. Method of measurement: Zigmond and Snaith Hospital Anxiety and Depression Questionnaire.

Secondary Outcome Measures

Name	Time	Method
The percentage of people who have a positive or negative pregnancy test result. Timepoint: 14 days after the sperm transfer process into the uterus. Method of measurement: Beta pregnancy blood test.