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NCT03762213 · ClinicalTrials.gov registry record · NA

Audio-Visual Relaxation Technology for Pediatric Amplified Musculoskeletal Pain Syndrome

A NA study, sponsored by Tufts Medical Center.

Completed
Registry status
NA
Development phase
30
Enrollment target

NCT03762213: Completed NA study, sponsored by Tufts Medical Center.

NCT03762213 is a NA study that has completed, run by Tufts Medical Center. The registered enrollment target is 30 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03762213, a NA study, has completed, sponsored by Tufts Medical Center.

COMPLETED
Registry status
NA
Development phase
30 participants
Enrollment target

Study Summary

A pilot randomized controlled trial to assess feasibility, acceptability and generate outcome domains for a future RCT testing the efficacy of immersive virtual reality on pain intensity in pediatric amplified musculoskeletal pain syndrome.

Primary Outcome

The VAS is a self-reported quantitative measure of pain intensity used commonly in clinical practice as well as in pain research. The VAS is a straight horizontal line of fixed length, usually 0 mm to 100 mm where 0 denotes 'no pain' and 100 denotes 'pain as bad as it could possibly be'. The participant marks a point on the line that they feel represents the perception of their current pain. The VAS score is then determined by measuring in millimeters from the left-hand end of the line to the po

Interventions

  • DEVICE Oculus GO VR HMD, application Happy Place (© Mimerse)
  • DEVICE iPad, application Happy Place (© Mimerse)

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2018-12-20
Est. Completion 2019-08-29
Phase NA
Tufts Medical Center

169 total trials

What the finished NCT03762213 record still lists

NCT03762213 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 2 interventions - of which Oculus GO VR HMD, application Happy Place (© Mimerse) is the first listed.

NCT03762213 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03762213 about?

NCT03762213 is a clinical study titled "Audio-Visual Relaxation Technology for Pediatric Amplified Musculoskeletal Pain Syndrome". A pilot randomized controlled trial to assess feasibility, acceptability and generate outcome domains for a future RCT testing the efficacy of immersive virtual reality on pain intensity in pediatric amplified musculoskeletal pain syndrome.

What is the current status of trial NCT03762213?

This trial is currently completed. It is a NA study. The enrollment target is 30 participants. The study started on 2018-12-20. Estimated completion is 2019-08-29.

What interventions are being tested in trial NCT03762213?

The interventions under investigation include: Oculus GO VR HMD, application Happy Place (© Mimerse) (DEVICE), iPad, application Happy Place (© Mimerse) (DEVICE).

Who is sponsoring clinical trial NCT03762213?

This trial is sponsored by Tufts Medical Center, which has 169 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03762213's enrollment target sits among peer trials

30 1593rd of 2000 higher than 299 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03762213, the US trial registry maintained by the National Library of Medicine. NCT03762213 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.