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Virtual Reality in MVA for Miscarriage

B

Barts & The London NHS Trust

Status

Completed

Conditions

Miscarriage

Treatments

Device: Virtual reality

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

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.

Full 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.

Enrollment

50 patients

Sex

Female

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

50 participants in 2 patient groups

Virtual reality for reduction of pain and anxiety during MVA
Active Comparator group
Description:
25 participants randomised to use VR headset during MVA and complete questionnaire and short interview regarding experience
Treatment:
Device: Virtual reality
Control group- no VR
No Intervention group
Description:
25 participants randomised to not use VR headset during MVA and complete questionnaire and short interview regarding experience

Trial documents
1

Trial contacts and locations

2

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Central trial contact

Nandita Deo, MRCOG; Anna A McDougall, MRCOG

Data sourced from clinicaltrials.gov

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