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NCT02615535 · ClinicalTrials.gov registry record · NA

Neurofeedback-enhanced Mindfulness Meditation in Traumatic Brain Injury

A NA study, sponsored by Spaulding Rehabilitation Hospital.

Completed
Registry status
NA
Development phase
25
Enrollment target

NCT02615535: Completed NA study, sponsored by Spaulding Rehabilitation Hospital.

NCT02615535 is a NA study that has completed, run by Spaulding Rehabilitation Hospital. The registered enrollment target is 25 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

NCT02615535, a NA study, has completed, sponsored by Spaulding Rehabilitation Hospital.

COMPLETED
Registry status
NA
Development phase
25 participants
Enrollment target

Study Summary

Spaulding Rehabilitation Hospital is conducting a research study evaluating the effectiveness of the brain-training product, MUSE, an EEG-guided neurofeedback device designed to assist in cultivating a relaxed, attentive state of mind during meditation. The investigators study aims to evaluate whether such a tool could be useful in treating persistent traumatic brain injury symptoms such as inattention, impulsivity, irritability, or dysregulated mood.

Primary Outcome

Measures common symptoms after head injury. This scales ranges from 0-4 on 22 items, for a minimum score of 0 and a maximum score of 88. Higher scores mean a greater severity of symptoms.

Interventions

  • DEVICE EEG neurofeedback-assisted meditation
  • DEVICE Non-EEG feedback-assisted meditation

Trial Details

FieldValue
Enrollment Target 25 participants
Start Date 2015-12
Est. Completion 2019-12
Phase NA
Spaulding Rehabilitation Hospital

101 total trials

What the finished NCT02615535 record still lists

NCT02615535 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 25 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 EEG neurofeedback-assisted meditation is the first listed.

NCT02615535 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02615535 about?

NCT02615535 is a clinical study titled "Neurofeedback-enhanced Mindfulness Meditation in Traumatic Brain Injury". Spaulding Rehabilitation Hospital is conducting a research study evaluating the effectiveness of the brain-training product, MUSE, an EEG-guided neurofeedback device designed to assist in cultivating a relaxed, attentive state of mind during meditation. The investigators study aims to evaluate wheth...

What is the current status of trial NCT02615535?

This trial is currently completed. It is a NA study. The enrollment target is 25 participants. The study started on 2015-12. Estimated completion is 2019-12.

What interventions are being tested in trial NCT02615535?

The interventions under investigation include: EEG neurofeedback-assisted meditation (DEVICE), Non-EEG feedback-assisted meditation (DEVICE).

Who is sponsoring clinical trial NCT02615535?

This trial is sponsored by Spaulding Rehabilitation Hospital, which has 101 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02615535's enrollment target sits among peer trials

25 1712th of 2000 higher than 265 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 NCT02615535, the US trial registry maintained by the National Library of Medicine. NCT02615535 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.