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Oxytocin, Trauma Disclosure and Intrusions

Effects of a Prolonged Oxytocin Treatment on Intrusions and Amygdala Reactivity in an Analogue Trauma Model

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03425929
Enrollment
70
Registered
2018-02-08
Start date
2016-06-01
Completion date
2017-03-18
Last updated
2018-02-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy

Keywords

amygdala, fear, intrusion, oxytocin, trauma disclosure

Brief summary

Severe traumatic experiences such as falling victim to assault, torture, or rape have deleterious effects. Clinical manifestations include intrusions, avoidance behavior, and hyperarousal, which are associated, at a circuit level, with hyperfunction of the amygdala and hypofunction of prefrontal cortex (PFC) subregions. In up to 50 % of the cases, resilience is not sufficient and trauma-exposed individuals develop posttraumatic stress disorder (PTSD). Oxytocin (OXT) is a hypothalamic peptide hormone that exerts anxiolytic effects. Recent clinical trials provide preliminary evidence that post-trauma administration of OXT could be effective as a preventive intervention for PTSD in a subsample of individuals exhibiting early PTSD symptoms prior to the onset of the disorder. However, the underlying neurobiological mechanisms are unclear. Therefore, the rationale of the present project is to expose a sample of healthy participants to experimental trauma in order to explore the circuit mechanisms by which OXT influences, and interferes with, traumatic experience. Functional magnetic resonance imaging (fMRI) will be employed in order to elucidate the long-term effects of intranasal OXT on trauma-induced intrusions, amygdala and PFC responses during an emotional face matching task and resting state functional connectivity.

Detailed description

Participants will be exposed to an experimental trauma (i.e. a highly aversive movie) at days 1 and 4 of the study. After the first experimental trauma and after the first functional magnetic resonance imaging (fMRI) measurement, the participants will receive intranasal OXT or placebo in three different groups (1. OXT for six days, 2. OXT for three days and then placebo for three days, 3. placebo for six days). The same fMRI tasks will be used after the first and second trauma exposure (i.e. one measurement before the treatment and one measurement after three days of treatment).

Interventions

DRUGOxytocin

Intranasal administration, 24 international units (IU) oxytocin.

DRUGPlacebo

The placebo nasal sprays contain identical ingredients except for the peptide itself.

Sponsors

University Hospital, Bonn
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy female volunteers * Right-handed

Exclusion criteria

* Current or past psychiatric disease * Current or past physical illness * Psychoactive medication * Hormonal contraception * MRI contraindication (e.g. metal in body, claustrophobia)

Design outcomes

Primary

MeasureTime frameDescription
Trauma disclosure (time spend discussing the movie)Six days following the first trauma movie exposure.The intrusion diaries will contain a question for how long participants discussed the trauma movie.
Total number of intrusions following the first trauma movie exposure.Three days following the first trauma movie exposure.The participants will be asked to complete intrusion diaries at home in the evening of the days 1 to 3. Intrusions will be defined as involuntary recollections relating to film events that appear, apparently spontaneously, in consciousness.
Total number of intrusions following the second trauma movie exposure.Three days following the second trauma movie exposure.The participants will be asked to complete intrusion diaries at home in the evening of the days 4 to 6. Intrusions will be defined as involuntary recollections relating to film events that appear, apparently spontaneously, in consciousness.
Neural responses to emotional faces in the amygdala.Neural activations will be measured with fMRI in an emotional face matching task that lasts 20 min.Functional magnetic resonance imaging (fMRI) will be performed to measure blood-oxygen-level dependent signal in response to emotional face stimuli. The investigators specifically plan to investigate amygdala responses to emotional faces, because pilot data indicate that neural responses to emotional faces in these regions are associated with the total number of intrusions.
Neural responses to emotional faces in the prefrontal cortex.Neural activations will be measured with fMRI in an emotional face matching task that lasts 20 min.Functional magnetic resonance imaging (fMRI) will be performed to measure blood-oxygen-level dependent signal in response to emotional face stimuli. The investigators specifically plan to investigate prefrontal cortex responses to emotional faces, because pilot data indicate that neural responses to emotional faces in these regions are associated with the total number of intrusions.
fMRI resting state dataFunctional data will be acquired for 6 min.Participants will be instructed to lie still with open eyes during the resting state measurement and not think of anything in particular.

Secondary

MeasureTime frameDescription
Changes in pupil diameter in response to the trauma movie2 min baseline before the trauma movie and during 15 min of the trauma movie.Changes in pupil diameter will be measured.
Changes in skin conductance level in response to the trauma movie2 min baseline before the trauma movie and during 15 min of the trauma movie.Changes in skin conductance level will be measured.
Changes in respiration rate in response to the trauma movie2 min baseline before the trauma movie and during 15 min of the trauma movie.Changes in respiration rate will be measured.
Salivary oxytocin concentrationsImmediately before the trauma movie, immediately after the trauma movie and 40 min after the trauma movie.Saliva samples will be collected before and after the trauma movie to assess changes in oxytocin concentrations.
Salivary cortisol concentrationsImmediately before the trauma movie, immediately after the trauma movie and 40 min after the trauma movie.Saliva samples will be collected before and after the trauma movie to assess changes in cortisol concentrations.
Questionnaire measurement of mood (PANAS)10 min before and 10 min after the trauma movie.Positive and negative affect will be assessed via self-rating questionnaire 'The Positive and Negative Affect Schedule' using a categorical 5 point scale.

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026