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Virtual Reality for pain relief during intrauterine device insertion

Virtual Reality for analgesia during intrauterine device insertion

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12622000088741
Enrollment
70
Registered
2022-01-24
Start date
2022-08-19
Completion date
2024-07-01
Last updated
2025-09-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Intrauterine devices (IUDs) are medical products placed inside the uterus to provide patients with reliable contraception but their use is often limited by pain at the time of insertion. Virtual reality (VR) is a technology that uses a headset to create a 3-dimensional interactive environment for the user and has been shown to be helpful for improving pain in other settings. This research project aims to find whether VR can help reduce the discomfort of having an IUD inserted. The study hypothesis is that VR will help to manage the pain of having an IUD inserted.

Interventions

Virtual reality (VR) is a technology that uses a headset to create a 3-dimensional interactive environment for the user. The user is therefore distracted from the real-world environment where the procedure is being done. It has been shown to be helpful for improving pain in other settings, for example burn victims. This research project aims to find whether VR can help reduce the discomfort of having an IUD inserted in the outpatient clinic setting. It also aims to discover whether it can help

Virtual reality (VR) is a technology that uses a headset to create a 3-dimensional interactive environment for the user. The user is therefore distracted from the real-world environment where the procedure is being done. It has been shown to be helpful for improving pain in other settings, for example burn victims. This research project aims to find whether VR can help reduce the discomfort of having an IUD inserted in the outpatient clinic setting. It also aims to discover whether it can help patients who feel anxious, and overall make it easier for the clinician to insert the IUD. Screening will occur in the Gynaecology outpatient clinic setting. Patients who are having IUD insertion in the clinic setting will be identified and approached for consent. Participants will be randomised to intervention and control groups. A researcher will give the patients in the intervention group a Smileyscope Pty Ltd. headset to deliver the VR experience. The headset will be worn and used for the duration of the IUD insertion procedure, which will last for approximately 5-10 minutes. It is the only addition to the standard care given. The headset will display a 4 minute proprietary virtual reality relaxation video displaying nature content. The control group will receive standard care. Study participants and the doctors inserting the IUD will answer questions about the procedure to help answer our questions about the usefulness of VR in this setting. If the VR intervention is discontinued during the IUD insertion procedure, this information, the reason and any adverse effects suffered will also be recorded.

Sponsors

Monash Health
Lead SponsorHospital

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

- Aged 18 years and over - Requiring IUD insertion - Able and willing to provide written informed consent

Exclusion criteria

- Patients with contraindications to IUD insertion - Patients with a history of epilepsy / vestibular disorders or other contraindications to VR use - Patients who have taken pain relief prior to the procedure - Inability to consent

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026