Wearable Emotion Prosthetics for Post Traumatic Stress Disorder
EP-PTSD
1 other identifier
interventional
16
1 country
1
Brief Summary
Involuntary stress reactions including hyper-reactivity and dissociation are key diagnostic features of many psychiatric disorders, are difficult to treat, and predict poor outcomes in conventional and neurobehavioral interventions. Here, we evaluate the extent to which a novel intervention, Tuned Vibroacoustic Stimulation (TVS), capitalizing on a preserved neurocircuitry for sympathetic and parasympathetic system activity can be used to modify arousal responses, overriding otherwise prepotent negative stress reactions. PTSD has been characterized by dysregulated responses to stress as a result of severe acute or chronic trauma resulting in significantly impaired functioning, quality of life, and morbidity/mortality. Physiologically, PTSD severity has been associated with elevated sympathetic tone and low heart rate variability suggesting that parasympathetic tone is suppressed. Lower heart rate variability specifically, as a measure of parasympathetic tone, is closely associated with impaired performance and resilience. In our first study (in review), we showed that in some individuals, TVS is associated with increased heart rate variability and performance under stress along with reduced subjective stress. These results suggest that TVS could provide some therapeutic benefit in PTSD. N=100 individuals with mild-moderate PTSD (as assessed by PCL-5/CAP5), at least half of which are military Veterans, will be assessed physiologically during active interventions. Mechanisms of attentional focus on cognitive and emotional stimuli will be assessed. Participants will also have a real-world intervention to determine if TVS helps alleviate stress, symptoms, and medication burden in the real world when stress has been identified. Success will suggest a new intervention pathway for a traditionally treatment-resistant dimension of psychopathology.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Apr 2018
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 9, 2018
CompletedFirst Submitted
Initial submission to the registry
April 16, 2018
CompletedFirst Posted
Study publicly available on registry
May 21, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 18, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
December 18, 2021
CompletedJanuary 28, 2022
January 1, 2022
3.7 years
April 16, 2018
January 13, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Change in symptom ratings from pre- to post-
Subjective affect / symptom ratings will be obtained daily. Spline fitting will be used to create a smoothed estimate of trajectory, the beginning and end points of which will be compared.
Change in symptom ratings over the approximately two weeks of the acute intervention (pre- to post- assessment)
Change in resting Heart Rate Variability (HRV) from pre- to post-
HRV, an index of parasympathetic reactivity, will be obtained throughout the day during the study. Increased HRV indicates increased parasympathetic reactivity, which suggests an increased physiological indicator of emotion regulation. Spline fitting will be used to create a smoothed estimate of trajectory, the beginning and end points of which will be compared.
HRV will be measured during the entire study which is two weeks
Secondary Outcomes (3)
Change in Heart Rate Variability (HRV) during information processing tasks (composite)
HRV will be measured during the approximately 1 hour of information processing tasks, which will be administered approximately 2 weeks apart, at the pre- and post- intervention assessment visits.
Galvanic skin response (GSR) during information processing tasks (composite)
GSR will be measured during the approximately 1 hour of information processing tasks, which will be administered approximately 2 weeks apart, at the pre- and post- intervention assessment visits.
prefrontal gamma band EEG during information processing tasks (composite)
EEG will be measured during the approximately 1 hour of information processing tasks, which will be administered approximately 2 weeks apart, at the pre- and post- intervention assessment visits.
Study Arms (2)
Stress incidents without TVS
ACTIVE COMPARATORa fraction of physiological detected stress incidents will not trigger TVS
TVS in response to participant initiation or stress detection
EXPERIMENTALThe majority of detected stress incidents will trigger TVS. Participants can also trigger TVS voluntarily
Interventions
TVS is an exteroceptive cue that may reduce subjective and physiological indicators of stress and increase behavioral performance
Eligibility Criteria
You may qualify if:
- Male/female who are 18 - 58 years of age
- For PTSD participants, must meet current DSM-V criteria for PTSD based on the PCL-5 (Score \> 33) and MINI PTSD Scale (administered in lab).
- If taking psychoactive medications, must be on a stable regimen for 3 weeks or more.
- Must have a functioning smartphone with Apple iOS or Android
You may not qualify if:
- Refusal or inability to provide informed consent
- Current suicidal or homicidal ideation with intent and/or plan that, in the judgment of the investigator, should be the focus of treatment.
- Current or recent (within the last 8 weeks) physically aggressive behavior.
- Meets current DSM-V criteria for substance dependence ((serious substance use in DSM-V parlance, not in remission) except nicotine and caffeine), traumatic brain injury, bipolar affective disorder, schizophrenia or any psychotic disorder.
- Has unstable or serious medical illness, including history of stroke, epileptic disorder, or unstable cardiac disease, that would interfere with participation in treatment.
- Taking medications that could affect thinking which must be taken on the day of testing, or dependence on psychoactive drugs (prescription or non-prescription) that could affect thinking. That is, participants need to be able to think clearly to complete the proposed information processing tasks. And they need to be able to learn to be able to make use of the intervention. Examples of drugs which could affect performance on cognitive tasks or the administered physiological measures include beta-blockers, benzodiazepines, antipsychotics, stimulants (except for treatment of ADD/ADHD), narcotics, and anti--Parkinsonian drugs.
- Severe cognitive impairment or severe trauma
- Unable to comprehend or communicate in English, and unable to complete questionnaires written in English.
- Having any eye problems or difficulties in corrected vision or hearing, including poor color vision
- Having a North American Adult Reading Test (NAART) equivalent FSIQ \< 85
- Severe or poorly controlled concurrent medical disorders or require medication that could cause negative thinking
- \-- Any electrical implant (pacemaker, vagus nerve stimulator, etc).
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Western Psychiatric Institute and Clinic
Pittsburgh, Pennsylvania, 15213, United States
Related Publications (37)
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PMID: 27769879RESULT
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Greg Siegle, MD
Western Psychiatric Institute and Clinic
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- QUADRUPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
- Masking Details
- On-demand intervention was provided on only some physiologically detected stress events
- Purpose
- BASIC SCIENCE
- Intervention Model
- FACTORIAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Professor
Study Record Dates
First Submitted
April 16, 2018
First Posted
May 21, 2018
Study Start
April 9, 2018
Primary Completion
December 18, 2021
Study Completion
December 18, 2021
Last Updated
January 28, 2022
Record last verified: 2022-01
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP, ICF, CSR, ANALYTIC CODE
- Time Frame
- Following publication - available to all. Before publication - upon negotiation with qualified investigators
- Access Criteria
- Before publication - available in negotiation with Greg Siegle (gsiegle@pitt.edu). After publication the location of a data repository will be listed
Following publication of primary results, individual anonymized data on primary outcome measures will be made available to other researchers. Before publication, primary outcome measures will be shared in negotiation with a proposed analysis plan from qualified investigators.