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NCT02970006 · ClinicalTrials.gov registry record · NA

Investigating Mechanisms Underlying Spinal Cord Stimulation Efficacy Using Virtual Reality and Full Body Illusion

A NA study, sponsored by Ohio State University.

Completed
Registry status
NA
Development phase
15
Enrollment target

NCT02970006: Completed NA study, sponsored by Ohio State University.

NCT02970006 is a NA study that has completed, run by Ohio State University. The registered enrollment target is 15 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02970006, a NA study, has completed, sponsored by Ohio State University.

COMPLETED
Registry status
NA
Development phase
15 participants
Enrollment target

Study Summary

The study hypothesis is that spinal cord stimulation (SCS) combined with virtual leg illumination (provided through a wearable headset (OculusRift, OculusVR, Irvine, CA) and a custom-designed virtual reality leg scenario) will lead to controlled analgesia induction, boosting analgesic effects obtained with standard SCS treatments and will further be associated with changes in the perception of the affected body part.

Primary Outcome

10 point Visual Analog pain rating Scale. Subjective pain perception will be measured by pain ratings on a 10cm visual continuous analog scale (VAS). Patients rate their pain, ranging from "no pain" (bottom part of the scale) to "the worst imaginable pain" (upper part of the scale) (Huskisson 1974). The pain reduction will be an average total of the pain scores taken at hours 1, 2, 3, 4, and 5.

Interventions

  • DEVICE neurovisual stimulation

Trial Details

FieldValue
Enrollment Target 15 participants
Start Date 2016-10
Est. Completion 2019-11
Phase NA
Ohio State University

552 total trials

What the finished NCT02970006 record still lists

NCT02970006 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 15 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 1 intervention - of which neurovisual stimulation is the first listed.

NCT02970006 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02970006 about?

NCT02970006 is a clinical study titled "Investigating Mechanisms Underlying Spinal Cord Stimulation Efficacy Using Virtual Reality and Full Body Illusion". The study hypothesis is that spinal cord stimulation (SCS) combined with virtual leg illumination (provided through a wearable headset (OculusRift, OculusVR, Irvine, CA) and a custom-designed virtual reality leg scenario) will lead to controlled analgesia induction, boosting analgesic effects obtain...

What is the current status of trial NCT02970006?

This trial is currently completed. It is a NA study. The enrollment target is 15 participants. The study started on 2016-10. Estimated completion is 2019-11.

What interventions are being tested in trial NCT02970006?

The interventions under investigation include: neurovisual stimulation (DEVICE).

Who is sponsoring clinical trial NCT02970006?

This trial is sponsored by Ohio State University, which has 552 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02970006's enrollment target sits among peer trials

15 1881st of 2000 higher than 92 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 NCT02970006, the US trial registry maintained by the National Library of Medicine. NCT02970006 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.