Evidence map›Paper›PMID 39316998›Full record

Trial reportPsychiatry research2024

A 4-week morning light treatment reduces amygdala reactivity and clinical symptoms in adults with traumatic stress.

Helen J Burgess, Muneer Rizvydeen, Brooke Huizenga, Masumi Prasad, Sonal Bahl, Elizabeth R Duval, Hyungjin Myra Kim, K Luan Phan, Israel Liberzon, James Abelson and 5 more

Registry-linked trialAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Psychiatry research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04117347 (Morning Light Treatment for Traumatic Stress), which is not on this map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–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.

NCT04117347 nacompletednot on this map

Morning Light Treatment for Traumatic Stress: The Role of Amygdala Reactivity

TypeinterventionalSponsorUniversity of MichiganRan2020 to 2023Enrolled50ConditionsStressArmsLight therapy A via the Re-Timer®, Light therapy B via the Re-Timer®, Light therapy C via the Re-Timer®
3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
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

15 authors.

Helen J BurgessDepartment of Psychiatry, University of Michigan, Ann Arbor, MI, USA. Electronic address: bhelen@med.umich.edu.
Muneer RizvydeenDepartment of Psychiatry, University of Michigan, Ann Arbor, MI, USA.
Brooke HuizengaDepartment of Psychiatry, University of Michigan, Ann Arbor, MI, USA.
Masumi PrasadDepartment of Psychiatry, University of Michigan, Ann Arbor, MI, USA.
Sonal BahlDepartment of Psychiatry, University of Michigan, Ann Arbor, MI, USA.
Elizabeth R DuvalDepartment of Psychiatry, University of Michigan, Ann Arbor, MI, USA.
Hyungjin Myra KimDepartment of Biostatistics, University of Michigan, Ann Arbor, MI, USA.
K Luan PhanDepartment of Psychiatry, Ohio State University, Columbus, OH, USA.
Israel LiberzonDepartment of Psychiatry, Texas A&M University, College Station, TX, USA.
James AbelsonDepartment of Psychiatry, University of Michigan, Ann Arbor, MI, USA.
Heide KlumppDepartment of Psychiatry, University of Illinois at Chicago, Chicago, IL, USA.
Adam HorwitzDepartment of Psychiatry, University of Michigan, Ann Arbor, MI, USA.
Ann MooneyDepartment of Psychiatry, University of Michigan, Ann Arbor, MI, USA.
Greta B RaglanDepartment of Psychiatry, University of Michigan, Ann Arbor, MI, USA.
Alyson K ZaltaDepartment of Psychological Science, University of California Irvine, Irvine, CA, USA.

Funding

Upgrade for MRI Instrument for Functional Brain ImagingS10OD026738 · OD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI NOLL, DOUGLAS C · 2019 to 2019
$1.8M
Morning Light Treatment for Traumatic Stress: the Role of Amygdala ReactivityR61MH117157 · NIMH · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BURGESS, HELEN JULIA, ZALTA, ALYSON KAY · 2019 to 2020
$1.6M
NIH HHS S10 OD026738NIMH NIH HHS R61 MH117157
6 · The paper itself

Abstract

Trauma leads to mental health problems including posttraumatic stress disorder (PTSD), depression, and anxiety. New treatments are needed for traumatic stress that can overcome barriers to care while targeting underlying biological mechanisms of the pathology. Morning light treatment has potential as a novel intervention for traumatic stress. We conducted a randomized clinical trial testing 3 doses of a 4-week morning light treatment in people with traumatic stress to evaluate brain mechanisms underlying the treatment. Forty-six participants completed a baseline week followed by a 4-week morning light treatment (15, 30 or 60 mins each morning). Functional magnetic resonance imaging was conducted at pre- and post-treatment using an emotional faces task to probe the amygdala, based on prior work showing direct effects of light on the amygdala and the role of amygdala in traumatic stress. Clinician-rated symptoms and self-reported symptoms were also assessed at pre- and post-treatment. No group differences were observed in left amygdala reactivity, but right amygdala reactivity reduced only in the 30 and 60 min groups with medium effect sizes. Clinical symptoms reduced in all groups with medium to large effect sizes. Self-reported depression and anxiety scores reduced more in the 60 min than in the 15 min group (p = .02). The results suggest that 4 weeks of morning light treatment of at least 30 min per day can reduce amygdala reactivity and symptoms of traumatic stress. Morning light treatment should be further explored as a potential treatment for traumatic stress, given it is relatively safe, acceptable, accessible and scalable.

Indexed as

AmygdalaMagnetic Resonance ImagingStress Disorders, Post-TraumaticAdultAnxietyDepressionFemaleHumansMaleMiddle AgedPhototherapyTreatment OutcomeYoung AdultActigraphyLightSleepStressTrauma

Identifiers

PMID39316998
PMCPMC11617273

What Socratic holds

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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 Socratic graph.