Evidence map›Paper›PMID 41584059›Full record

ArticleContemporary clinical trials communications2026

A mechanistic trial of the neurobiology of extinction learning and intraparietal sulcus stimulation: Protocol.

Sonalee A Joshi, Tao Lin, Nicholas L Balderston, Kevin G Lynch, Mingcong Tang, Milan Patel, Ivy Sun, Barbara Fureman, Desmond J Oathes, David F Gregory and 2 more

Abstract read
In one paragraph

Article in Contemporary clinical trials communications, 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

12 authors.

Sonalee A JoshiDepartment of Psychiatry, University of Pennsylvania, Philadelphia, PA, United States.
Tao LinDepartment of Psychiatry, University of Pennsylvania, Philadelphia, PA, United States.
Nicholas L BalderstonDepartment of Psychiatry, University of Pennsylvania, Philadelphia, PA, United States.
Kevin G LynchDepartment of Psychiatry, University of Pennsylvania, Philadelphia, PA, United States.
Mingcong TangDepartment of Psychiatry, University of Pennsylvania, Philadelphia, PA, United States.
Milan PatelDepartment of Psychiatry, University of Pennsylvania, Philadelphia, PA, United States.
Ivy SunDepartment of Psychiatry, University of Pennsylvania, Philadelphia, PA, United States.
Barbara FuremanDepartment of Psychiatry, University of Pennsylvania, Philadelphia, PA, United States.
Desmond J OathesDepartment of Psychiatry, University of Pennsylvania, Philadelphia, PA, United States.
David F GregoryDepartment of Psychiatry, University of Pennsylvania, Philadelphia, PA, United States.
Yvette I ShelineDepartment of Psychiatry, University of Pennsylvania, Philadelphia, PA, United States.
Lily A BrownDepartment of Psychiatry, University of Pennsylvania, Philadelphia, PA, United States.

Funding

Translational Research Support CoreP30ES013508 · NIEHS · UNIVERSITY OF PENNSYLVANIA · PI A. Clementina Mesaros · 2006 to 2026
$35.3M
Penn Mental Health AIDS Research CenterP30MH097488 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI Karine Dube, Kelly L Jordan-Sciutto · 2013 to 2026
$23.5M
A mechanistic trial of the neurobiology of extinction learning and intraparietal sulcus stimulationR01MH132740 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI Lily A Brown · 2024 to 2026
$2.4M
NIEHS NIH HHS P30 ES013508NIMH NIH HHS P30 MH097488NIMH NIH HHS R01 MH132740
6 · The paper itself

Abstract

Post-traumatic stress disorder (PTSD) links to impaired extinction learning post-trauma. While treatments like prolonged exposure therapy improve this learning, they benefit only 40-60 % of patients. Optimal arousal supports extinction learning, but excessive arousal can hinder it. The intraparietal sulcus (IPS) is involved in arousal regulation but has not yet been targeted using continuous theta burst stimulation (cTBS) in PTSD. This study is the first to explore the effect of IPS cTBS on extinction learning in PTSD. This study aims to 1) evaluate the impact of IPS cTBS on anxiety potentiated startle (APS) among patients with PTSD compared to sham IPS cTBS, 2) examine whether IPS cTBS improves extinction learning relative to neutral learning, and 3) identify the ideal dose of cTBS. Adults with PTSD will participate in six visits, involving clinical assessments, functional MRI (fMRI), and IPS cTBS. Participants will undergo diagnostic interviews, generate trauma and neutral scripts, and complete script-driven imagery tasks. They will receive active or sham cTBS (counterbalanced) paired with trauma or neutral scripts during separate visits. Follow-up assessments occur at 24 h and 30 days post-intervention. IRB approval and preliminary preparations began in January 2024. Recruitment started in April 2024 and is projected to conclude by April 2028. Ethical procedures are approved by the University of Pennsylvania IRB (Protocol Number: 849571). This will be the first study to evaluate the synergistic effects of extinction training with IPS cTBS in individuals with PTSD. Our findings will strengthen the neurobiological basis of augmenting extinction training with IPS cTBS.

Indexed as

Continuous theta burst stimulationNeuromodulationPosttraumatic stress disorder (PTSD)Transcranial magnetic stimulation

Identifiers

PMID41584059
PMCPMC12828414

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Registered trials

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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.