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NCT05169346 · ClinicalTrials.gov registry record · NA

Neurofeedback to Treat Depression

A NA study, sponsored by University of Pennsylvania.

Completed
Registry status
NA
Development phase
71
Enrollment target

NCT05169346: Completed NA study, sponsored by University of Pennsylvania.

NCT05169346 is a NA study that has completed, run by University of Pennsylvania. The registered enrollment target is 71 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT05169346, a NA study, has completed, sponsored by University of Pennsylvania.

COMPLETED
Registry status
NA
Development phase
71 participants
Enrollment target

Study Summary

This study tests the efficacy of a new psychotherapeutic strategy for reducing negative attention bias (and therefore depression severity) in participants with MDD (60 in R61 phase and 80 in R33 Phase). This real-time fMRI neurofeedback therapy uses cloud-based pattern classification to decode a patient's attentional state and dynamically modulate task stimuli (in a closed loop) based on this state.

Primary Outcome

Associate neurofeedback related changes in our hypothesized attentional mechanism of depression (i.e. neural perseveration of negative states) with changes in depression severity as measured by the Montgomery Asberg Depression Rating Scale (MADRS).

Interventions

  • BEHAVIORAL Active Closed Loop Real Time fMRI Neurofeedback
  • BEHAVIORAL Sham Closed Loop Real Time fMRI Neurofeedback

Trial Details

FieldValue
Enrollment Target 71 participants
Start Date 2022-05-25
Est. Completion 2025-06-13
Phase NA
University of Pennsylvania

1,423 total trials

What the finished NCT05169346 record still lists

NCT05169346 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 71 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower).

The record links to 0 conditions, and to 2 interventions - of which Active Closed Loop Real Time fMRI Neurofeedback is the first listed.

NCT05169346 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05169346 about?

NCT05169346 is a clinical study titled "Neurofeedback to Treat Depression". This study tests the efficacy of a new psychotherapeutic strategy for reducing negative attention bias (and therefore depression severity) in participants with MDD (60 in R61 phase and 80 in R33 Phase). This real-time fMRI neurofeedback therapy uses cloud-based pattern classification to decode a pat...

What is the current status of trial NCT05169346?

This trial is currently completed. It is a NA study. The enrollment target is 71 participants. The study started on 2022-05-25. Estimated completion is 2025-06-13.

What interventions are being tested in trial NCT05169346?

The interventions under investigation include: Active Closed Loop Real Time fMRI Neurofeedback (BEHAVIORAL), Sham Closed Loop Real Time fMRI Neurofeedback (BEHAVIORAL).

Who is sponsoring clinical trial NCT05169346?

This trial is sponsored by University of Pennsylvania, which has 1,423 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05169346's enrollment target sits among peer trials

71 1102nd of 2000 higher than 898 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 NCT05169346, the US trial registry maintained by the National Library of Medicine. NCT05169346 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.