Evidence map›Paper›PMID 29696166›Full record

ArticleContemporary clinical trials communications2017

Design, rationale and feasibility of a multidimensional experimental protocol to study early life stress.

M Dillwyn Bartholomeusz, Philip S Bolton, Robin Callister, Virginia Skinner, Deborah Hodgson

Abstract read
In one paragraph

Article in Contemporary clinical trials communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

5 authors.

M Dillwyn BartholomeuszSchool of Psychology, Faculty of Science, University of Newcastle, Callaghan, NSW 2308, Australia.
Philip S BoltonSchool of Biomedical Sciences & Pharmacy, Faculty of Health, University of Newcastle, Callaghan, NSW 2308, Australia.
Robin CallisterSchool of Biomedical Sciences & Pharmacy, Faculty of Health, University of Newcastle, Callaghan, NSW 2308, Australia.
Virginia SkinnerOffice of the Chief Nursing and Midwifery Officer, Department of Health, Northern Territory Government, University Fellow Charles Darwin University, PO Box 40596, Casuarina, NT 0811, Australia.
Deborah HodgsonSchool of Psychology, Faculty of Science, University of Newcastle, Callaghan, NSW 2308, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is a rapidly accumulating body of evidence regarding the influential role of early life stress (ELS) upon medical and psychiatric conditions. While self-report instruments, with their intrinsic limitations of recall, remain the primary means of detecting ELS in humans, biological measures are generally limited to a single biological system. This paper describes the design, rationale and feasibility of a study to simultaneously measure neuroendocrine, immune and autonomic nervous system (ANS) responses to psychological and physiological stressors in relation to ELS. Five healthy university students were recruited by advertisement. Exclusion criteria included chronic medical conditions, psychotic disorders, needle phobia, inability to tolerate pain, and those using anti-inflammatory medications. They were clinically interviewed and physiological recordings made over a two-hour period pre, during and post two acute stressors: the cold pressor test and recalling a distressing memory. The Childhood Trauma Questionnaire and the Parental Bonding Index were utilised to measure ELS. Other psychological measures of mood and personality were also administered. Measurements of heart rate, blood pressure, respiratory rate, skin conductance, skin blood flow and temporal plasma samples were successfully obtained before, during and after acute stress. Participants reported the extensive psychological and multisystem physiological data collection and stress provocations were tolerable. Most (4/5) participants indicated a willingness to return to repeat the protocol, indicating acceptability. Our protocol is viable and safe in young physically healthy adults and allows us to assess simultaneously neuroendocrine, immune and autonomic nervous system responses to stressors in persons assessed for ELS.

Indexed as

Adverse-childhood-eventsANS, Autonomic nervous systemChildhood-stressChildhood-trauma questionnaireCPT, Cold pressor testCTQ, Childhood Trauma QuestionnaireDASS, Depression, Anxiety and Stress ScaleDS14, Type D ScaleECG, lectrocardiogramELS, Early life stressEPQRs, Eysenck Personality Questionnaire Revised – short formHPA, Hypothalamic-pituitary-adrenalParental-bonding-instrumentPBI, Parental Bonding InstrumentPTSD, Post-traumatic Stress DisorderRDM, Recall of distressing memoryType D scale (DS14)

Identifiers

PMID29696166
PMCPMC5898516

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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.