Evidence map›Paper›PMID 28407727›Full record

Trial reportThe American journal of psychiatry2017

Randomized Clinical Trial of Real-Time fMRI Amygdala Neurofeedback for Major Depressive Disorder: Effects on Symptoms and Autobiographical Memory Recall.

Kymberly D Young, Greg J Siegle, Vadim Zotev, Raquel Phillips, Masaya Misaki, Han Yuan, Wayne C Drevets, Jerzy Bodurka

4 registry-linked trialsOpen access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in The American journal of psychiatry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 4 registered trials, which are not on this map. Cited by 162 papers, 15 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
162citing papers in PubMed, 15 pooled it
18.7field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03428828 nacompletednot on this mapstarted 2018, after this paper: background citation

Amygdala rtfMRI Neurofeedback for Treatment Resistant Depression

TypeinterventionalSponsorKymberly YoungRan2018 to 2026Enrolled60ConditionsTreatment Resistant DepressionArmsAmygdala Neurofeedback, Parietal Neurofeedback
NCT05627895 completednot on this mapstarted 2023, after this paper: background citation

A Feasibility Study of fMRI-neurofeedback in Parkinson's Disease

TypeobservationalSponsorMaastricht UniversityRan2023 to 2024Enrolled12ConditionsBasal-ganglia fMRI NeurofeedbackArmsNeurofeedback
NCT05703256 narecruitingnot on this mapstarted 2023, after this paper: background citation

Confirmatory Efficacy Randomized Clinical Trial of Amygdala Neurofeedback for Major Depressive Disorder

TypeinterventionalSponsorKymberly YoungRan2023 to 2028Enrolled200ConditionsMajor Depressive DisorderArmsAmygdala real-time fMRI neurofeedback, Sham feedback
NCT06582355 narecruitingnot on this mapstarted 2025, after this paper: background citation

MOTOR-NF - a Randomized Controlled Trial of FMRI-based Neurofeedback for Motor Symptoms of Parkinson's Disease

TypeinterventionalSponsorMaastricht University Medical CenterRan2025 to 2026Enrolled60ConditionsParkinson DiseaseArmsNeurofeedback, Kinesthetic imagery
3 · Its place in the literature

Who cites it

162 citing papers in PubMed, 15 syntheses or guidelines pooled it, 354 citations in OpenAlex.

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  5. Mood-congruent memory revisited.Psychological review · 2023
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102 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Kymberly D YoungFrom the Laureate Institute for Brain Research, Tulsa, Okla.; the Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh; the Stephenson School of Biomedical Engineering, University of Oklahoma, Norman; Janssen Research and Development, New Brunswick, N.J.; and the Biomedical Engineering Center, University of Oklahoma College of Engineering, Norman.
Greg J SiegleFrom the Laureate Institute for Brain Research, Tulsa, Okla.; the Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh; the Stephenson School of Biomedical Engineering, University of Oklahoma, Norman; Janssen Research and Development, New Brunswick, N.J.; and the Biomedical Engineering Center, University of Oklahoma College of Engineering, Norman.
Vadim ZotevFrom the Laureate Institute for Brain Research, Tulsa, Okla.; the Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh; the Stephenson School of Biomedical Engineering, University of Oklahoma, Norman; Janssen Research and Development, New Brunswick, N.J.; and the Biomedical Engineering Center, University of Oklahoma College of Engineering, Norman.
Raquel PhillipsFrom the Laureate Institute for Brain Research, Tulsa, Okla.; the Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh; the Stephenson School of Biomedical Engineering, University of Oklahoma, Norman; Janssen Research and Development, New Brunswick, N.J.; and the Biomedical Engineering Center, University of Oklahoma College of Engineering, Norman.
Masaya MisakiFrom the Laureate Institute for Brain Research, Tulsa, Okla.; the Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh; the Stephenson School of Biomedical Engineering, University of Oklahoma, Norman; Janssen Research and Development, New Brunswick, N.J.; and the Biomedical Engineering Center, University of Oklahoma College of Engineering, Norman.
Han YuanFrom the Laureate Institute for Brain Research, Tulsa, Okla.; the Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh; the Stephenson School of Biomedical Engineering, University of Oklahoma, Norman; Janssen Research and Development, New Brunswick, N.J.; and the Biomedical Engineering Center, University of Oklahoma College of Engineering, Norman.
Wayne C DrevetsFrom the Laureate Institute for Brain Research, Tulsa, Okla.; the Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh; the Stephenson School of Biomedical Engineering, University of Oklahoma, Norman; Janssen Research and Development, New Brunswick, N.J.; and the Biomedical Engineering Center, University of Oklahoma College of Engineering, Norman.
Jerzy BodurkaFrom the Laureate Institute for Brain Research, Tulsa, Okla.; the Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh; the Stephenson School of Biomedical Engineering, University of Oklahoma, Norman; Janssen Research and Development, New Brunswick, N.J.; and the Biomedical Engineering Center, University of Oklahoma College of Engineering, Norman.
University of Oklahoma · US

Funding

Effects of amygdala neurofeedback on depressive symptoms and processing biasesK99MH101235 · NIMH · LAUREATE INSTITUTE FOR BRAIN RESEARCH · PI YOUNG, KYM · 2014 to 2015
$179k
NIMH NIH HHS K99 MH101235
6 · The paper itself

Abstract

objectivePatients with depression show blunted amygdala hemodynamic activity to positive stimuli, including autobiographical memories. The authors examined the therapeutic efficacy of real-time functional MRI neurofeedback (rtfMRI-nf) training aimed at increasing the amygdala's hemodynamic response to positive memories in patients with depression.

methodIn a double-blind, placebo-controlled, randomized clinical trial, unmedicated adults with depression (N=36) were randomly assigned to receive two sessions of rtfMRI-nf either from the amygdala (N=19) or from a parietal control region not involved in emotional processing (N=17). Clinical scores and autobiographical memory performance were assessed at baseline and 1 week after the final rtfMRI-nf session. The primary outcome measure was change in score on the Montgomery-Åsberg Depression Rating Scale (MADRS), and the main analytic approach consisted of a linear mixed-model analysis.

resultsIn participants in the experimental group, the hemodynamic response in the amygdala increased relative to their own baseline and to the control group. Twelve participants in the amygdala rtfMRI-nf group, compared with only two in the control group, had a >50% decrease in MADRS score. Six participants in the experimental group, compared with one in the control group, met conventional criteria for remission at study end, resulting in a number needed to treat of 4. In participants receiving amygdala rtfMRI-nf, the percent of positive specific memories recalled increased relative to baseline and to the control group.

conclusionsrtfMRI-nf training to increase the amygdala hemodynamic response to positive memories significantly decreased depressive symptoms and increased the percent of specific memories recalled on an autobiographical memory test. These data support a role of the amygdala in recovery from depression.

Indexed as

Memory, EpisodicAdolescentAdultAmygdalaDouble-Blind MethodFemaleHemodynamicsHumansImage Interpretation, Computer-AssistedMagnetic Resonance ImagingMajor Depressive DisorderMaleMiddle AgedNeurofeedbackYoung AdultBrain Imaging TechniquesEmotionfMRI neurofeedbackMemoryMood Disorders-UnipolarOther Psychosocial Techniques/Treatments

Identifiers

PMID28407727
PMCPMC5538952
OpenAlexW2607313129

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.