Evidence map›Paper›PMID 33206061›Full record

ArticleJMIR research protocols2020

Posttraumatic Stress Disorder and Neuroprogression in Women Following Sexual Assault: Protocol for a Randomized Clinical Trial Evaluating Allostatic Load and Aging Process Acceleration.

Bruno Messina Coimbra, Mary Yeh, Ana Teresa D'Elia, Mariana Rangel Maciel, Carolina Muniz Carvalho, Ana Carolina Milani, Adriana Mozzambani, Mario Juruena, Sintia Iole Belangero, Andrea Parolin Jackowski and 3 more

Abstract read
In one paragraph

Article in JMIR research protocols, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

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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

13 authors.

Bruno Messina CoimbraDepartment of Psychiatry, Universidade Federal de São Paulo, São Paulo, Brazil.ORCID https://orcid.org/0000-0001-5092-9625
Mary YehDepartment of Psychiatry, Universidade Federal de São Paulo, São Paulo, Brazil.ORCID https://orcid.org/0000-0003-0958-1860
Ana Teresa D'EliaDepartment of Psychiatry, Universidade Federal de São Paulo, São Paulo, Brazil.ORCID https://orcid.org/0000-0002-9891-5123
Mariana Rangel MacielDepartment of Psychiatry, Universidade Federal de São Paulo, São Paulo, Brazil.ORCID https://orcid.org/0000-0002-1428-3553
Carolina Muniz CarvalhoDepartment of Psychiatry, Universidade Federal de São Paulo, São Paulo, Brazil.ORCID https://orcid.org/0000-0002-3376-9831
Ana Carolina MilaniDepartment of Psychiatry, Universidade Federal de São Paulo, São Paulo, Brazil.ORCID https://orcid.org/0000-0002-9190-654X
Adriana MozzambaniDepartment of Psychiatry, Universidade Federal de São Paulo, São Paulo, Brazil.ORCID https://orcid.org/0000-0002-4145-0003
Mario JuruenaCentre for Affective Disorders, Department of Psychological Medicine, Institute of Psychiatry, Psychology and Neuroscience, Biomedical Research Centre, South London and Maudsley NHS Foundation Trust and King's College, London, United Kingdom.ORCID https://orcid.org/0000-0001-8558-3396
Sintia Iole BelangeroDepartment of Psychiatry, Universidade Federal de São Paulo, São Paulo, Brazil.ORCID https://orcid.org/0000-0002-2419-4351
Andrea Parolin JackowskiDepartment of Psychiatry, Universidade Federal de São Paulo, São Paulo, Brazil.ORCID https://orcid.org/0000-0001-8842-5406
Dalva PoyaresDepartment of Psychobiology, Universidade Federal de São Paulo, São Paulo, Brazil.ORCID https://orcid.org/0000-0003-0664-0968
Andrea Feijo MelloDepartment of Psychiatry, Universidade Federal de São Paulo, São Paulo, Brazil.ORCID https://orcid.org/0000-0001-8498-7751
Marcelo Feijo MelloDepartment of Psychiatry, Universidade Federal de São Paulo, São Paulo, Brazil.ORCID https://orcid.org/0000-0002-0475-4729

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPosttraumatic stress disorder (PTSD) is a prevalent, chronic, and severe disorder related to traumatic events. Women are disproportionately affected by PTSD than men and are more at risk in the occurrence of sexual assault victimization. Estimates suggest that 50% of women develop PTSD following sexual assault and successful clinical management can be challenging. Growing evidence has implicated neural, immune, and endocrine alterations underpinning PTSD, but only few studies have assessed the evolution of acute PTSD in women.

objectiveThis study aims to measure whether the onset of PTSD is associated with accelerated aging in women following sexual assault. We hypothesize that the increase of allostatic load caused by PTSD leads to neuroprogression. We will implement a randomized clinical trial to compare responses to treatment with either interpersonal psychotherapy adapted for PTSD (IPT-PTSD) or the selective serotonin reuptake inhibitor sertraline.

methodsWe will include women between 18 and 45 years of age, who experienced sexual assault from 1 to 6 months before the initial evaluation, and present with a Diagnostic and Statistical Manual of Mental Disorders, fifth edition (DSM-5) diagnosis of PTSD. Baseline evaluation will comprise clinical and psychometric assessments, structural and functional magnetic resonance imaging, neuropsychological testing, polysomnography, evaluation of immune and endocrine parameters, and genetic analyses. Age-matched female healthy controls will be included and subjected to the same evaluation. Patients will be randomized for treatment in 1 of the 2 arms of the study for 14 weeks; follow-up will continue until 1 year after inclusion via treatment as usual. The researchers will collect clinical and laboratory data during periodic clinical assessments up to 1-year follow-up.

resultsData collection started in early 2016 and will be completed by the end of the first semester of 2020. Analyses will be performed soon afterward, followed by the elaboration of several articles. Articles will be submitted in early 2021. This research project has obtained a grant from the Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP 2014/12559-5).

conclusionsWe expect to provide insight into the consequences of recent sexual assault exposure in women by investigating the degree of neuroprogression developing from an early stage of PTSD. We also expect to provide important evidence on the efficacy of a non-exposure psychotherapy (IPT-PTSD) to mitigate PTSD symptoms in recently sexually assaulted women. Further, we aim to obtain evidence on how treatment outcomes are associated with neuroprogression measures.

trial registrationBrazilian Clinical Trials Registry RBR-3z474z; http://www.ensaiosclinicos.gov.br/rg/RBR-3z474z/. INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): DERR1-10.2196/19162.

Indexed as

agingallostatic loadneuroprogressionPTSDrandomized clinical trialsexual assaultthematic researchtrauma

Identifiers

PMID33206061
PMCPMC7710442

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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.