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Clinical Trials/NCT04466956
NCT04466956
Completed
Not Applicable

Virtual Reality as a Distraction Technique for the Management of Acute Pain and Anxiety During Manual Vacuum Aspiration for Miscarriage

Barts & The London NHS Trust2 sites in 1 country50 target enrollmentJuly 1, 2021
ConditionsMiscarriage

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Miscarriage
Sponsor
Barts & The London NHS Trust
Enrollment
50
Locations
2
Primary Endpoint
Anxiety Rating
Status
Completed
Last Updated
last year

Overview

Brief Summary

We are investigating the use of a virtual reality programme to reduce pain and anxiety experienced during manual vacuum aspiration.

Virtual reality (VR) is the computer-generated simulation of a three-dimensional environment that can be interacted with in a seemingly real way by a person using special electronic equipment. In this study a VR headset is worn by the patient allowing them to experience a relaxing environment whilst the procedure manual vacuum aspiration (MVA) is performed.

VR is mostly used in computer gaming but has uses in medical field and has been used in the treatment of long standing pain, treatment of burns, dentistry and treatment of cancer pain. However, its role in the management of pain and anxiety during gynaecological procedures like manual vacuum aspiration has not been researched. This study explores whether it has a place in the treatment of gynaecological pain and reduction of anxiety.

Detailed Description

Many simple gynaecological procedures can be performed in an outpatient setting without the need for general anaesthesia. Such office-based procedures include outpatient hysteroscopy, endometrial biopsy, large-loop-excision of the transformation zone and manual vacuum aspiration for the management of miscarriage. Advantages experienced by patients include reduced anaesthetic risk, enhanced recovery time and flexibility of timings. For the healthcare provider there are significant cost benefits on the basis of reduced theatre time, staff and equipment. Patient satisfaction is generally high but influenced by their experience of pain and feelings of anxiety before, during and after the procedure. The rationale for this study is to invetsigate the role of distraction techniques and the feasibility of using virtual reality for the management of acute pain and anxiety experienced by patients undergoing manual vacuum aspiration Primary objective • Feasibility of using virtual reality as a distraction technique in management of acute pain and anxiety in patients undergoing manual vacuum aspiration for miscarriage. Secondary objectives * Understanding the acceptability and effectiveness of VR interventions in office gynaecology procedures * Understanding the factors that might influence the willingness of patients to participate in a future formal trial of the technology. * Understanding how best to implement the technology and designing of the contents of the VR intervention.

Registry
clinicaltrials.gov
Start Date
July 1, 2021
End Date
January 27, 2023
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients: Clinical indications for undergoing an MVA will be confirmed. Inclusion criteria will include all women of 18 - 50 years of age, planned for a MVA who are able and willing to give informed consent.

Exclusion Criteria

  • Hearing impairments and blindness
  • History of epilepsy or any previous seizures
  • Any known anatomical characteristics that may make performing the office procedure more difficult (e.g., cervical conisation)
  • Any known characteristics that make the patient unsuitable for undergoing MVA (e.g. known bleeding disorder, gestation \>12 weeks)
  • The denial or withdrawal of informed consent

Outcomes

Primary Outcomes

Anxiety Rating

Time Frame: 12 months

Anxiety score (numerical rating score 0 least-10 worst) and questionnaire

Pain Rating

Time Frame: 12 months

Pain score (numerical rating score 0 least-10 worst) and questionnaire

Study Sites (2)

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