Virtual Reality as a tool for counselling about office hysteroscopy can reduce anxiety
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/07/071148
- Lead Sponsor
- Tanvir
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Women above 18 years of age planned for OH. Those who are able to provide informed consent.
Exclusion Criteria
Those who have hearing problems. Those who cannot give consent. Those who decline participation. Women who have undergone previous office hysteroscopy by vaginoscopy technique. Women with a prior history of psychological disease.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome measured is the comparison of preoperative anxiety scores as assessed by <br/ ><br>VAS - A, in both interventional and control groups.Timepoint: At baseline
- Secondary Outcome Measures
Name Time Method To compare the postoperative pain scores, success rate & Likert scale of satisfaction in the interventional group & the control group.Timepoint: At baseline