Evidence map›Paper›PMID 42763338›Full record

ArticleMolecular psychiatry2026

Targeting the dopaminergic midbrain with precision 7-Tesla biofeedback training in depression: A proof-of-principle randomized controlled trial.

Laurel S Morris, Jacqueline M Beltrán, Timo L Kvamme, Avijit Chowdhury, Grace Butler, Abigail Adams, Tanvi Patel, Emerald Obie, Samantha Fontaine, Morgan Corniquel and 6 more

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular psychiatry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Laurel S MorrisDepartment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, USA. laurel.morris@mssm.edu.ORCID http://orcid.org/0000-0002-5862-6650
Jacqueline M BeltránDepartment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Timo L KvammeDepartment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, USA.ORCID http://orcid.org/0000-0002-3479-4297
Avijit ChowdhuryDepartment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Grace ButlerDepartment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Abigail AdamsDepartment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Tanvi PatelDepartment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Emerald ObieDepartment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Samantha FontaineDepartment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Morgan CorniquelDepartment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Marishka M MehtaDepartment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, USA.ORCID http://orcid.org/0000-0001-5105-6723
Derek A SmithBioMedical Engineering and Imaging Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Lazar FleysherBioMedical Engineering and Imaging Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Priti BalchandaniBioMedical Engineering and Imaging Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.ORCID http://orcid.org/0000-0001-7709-5835
Yael JacobDepartment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, USA.ORCID http://orcid.org/0000-0003-3278-9264
James W MurroughDepartment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, USA.ORCID http://orcid.org/0000-0001-6286-1242

Funding

Carlsbergfondet (Carlsberg Foundation) CF22-0132
6 · The paper itself

Abstract

The significant heterogeneity of major depressive disorder (MDD) requires the development of interventions that directly target underlying cognitive or neurobiological mechanisms. This work tested the efficacy of self-modulation of the dopaminergic midbrain with high-field 7-Tesla functional MRI biofeedback in a randomized, controlled, proof-of-principle trial that targeted motivation regulation. A total of N = 62 unmedicated participants (MDD and healthy controls) were randomized to receive either Active or Sham 7-Tesla functional MRI biofeedback and completed clinical assessments pre- and up to 30-days post-training. Factor analysis of clinical symptom change revealed a single latent clinical improvement factor that was significantly improved in the Active MDD compared to the Sham MDD group, immediately post-training (β = 15.85, t = 2.31, p = 0.03), and at 24-hours post-training (β = 22.84, t = 2.45, p = 0.02); effects were diminished and no longer significant at 7-day and 30-day follow-ups. Results of specific phenotypic clinical analysis revealed that depressed mood (F = 5.04, p = 0.029) and negative affect (F = 5.21, p = 0.027), but not positive affect, were most improved by the Active biofeedback intervention. Active biofeedback training engaged functional coupling over time between the VTA and the lateral frontal cortex in the MDD group (F = 6.03, p = 0.017), and greater overall VTA regulation was associated with clinical improvement (R = 0.268, p = 0.048). Together, these results indicate the potential utility of dopaminergic midbrain-based biofeedback training for improvement of mood and negative affect in MDD.

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.