BridgeMD
New treatment option for PTSD - Post Traumatic Stress Disorder
Official title REVEAL Study - Diagnostic Testing for PTSD Using the Senseye Diagnostic Tool
ClinicalTrials.gov ID: NCT07280065
What this study is testing
- What it's testing
- The goal of the REVEAL PTSD study is to test how well the Senseye DT works as a diagnostic test for Post-traumatic Stress Disorder (PTSD) in adults 18 and older who are experiencing one or more symptoms that might be related to PTSD. The Senseye DT is software as a medical device (SaMD) and is an iPhone app that administers a series of simple tasks on the phone while recording video during the tasks through the front-facing camera.
- Phase 3: a large, late-stage study
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older. Healthy volunteers may be eligible.
You may be able to join if
- The participant is willing and able to read, understand, and sign the approved Informed Consent Form (ICF).
- Age 18 years old or older.
- In the past month, participant presents with at least one of the following:
- nightmares or unwanted, intrusive thoughts
- avoidance of specific thoughts or situations
You likely can't join if
- Current diagnosis of epilepsy and/or other seizure disorders.
- A history of at Screening OR positive at Visit 1 for bipolar I or II, mania, or one or more schizophrenia-spectrum or other psychotic disorders...
- Compromised facial neuro-ophthalmic integrity (e.g., due to stroke, MS, ALS, or other neurological conditions).
- Current diagnosis of dementia, delirium, amnestic disorders, autism, hydrocephalus, posterior cortical atrophy, aphasia, multiple sclerosis, or...
- Current eye disorders which prevent the patient from using the Senseye DT:
- Vision impairment preventing ability to read with correction (including corneal disease, dense cataract, diabetic retinopathy, macular degeneration...
See the full eligibility criteria
Who can join
- The participant is willing and able to read, understand, and sign the approved Informed Consent Form (ICF).
- Age 18 years old or older.
- In the past month, participant presents with at least one of the following:
- nightmares or unwanted, intrusive thoughts
- avoidance of specific thoughts or situations
- feelings of being constantly on guard, watchful, or easily startled
- feeling numb or detached from people, activities, or surroundings; and/or
- persistent feelings of guilt or self blame for things that have happened.
- excessive anxiety and worry (apprehensive expectation), occurring more days than not for at least 6 months, about a number of events or activities (such as work or school performance)
- sleep disturbance (difficulty falling or staying asleep, or restless unsatisfying sleep)
- depressed mood: most of the day, nearly every day, feeling sad, empty, or hopeless
- markedly diminished interest or pleasure in activities: loss of interest or pleasure in most activities, nearly every day
- self-report of significant weight loss or gain and/or changes in appetite
- insomnia or hypersomnia: sleeping too little or too much
- psychomotor agitation or retardation: observable restlessness or slowed movements
- abnormal fatigue or loss of energy: feeling tired or lacking energy more than usual
- Deemed likely to comply with the study protocol by the study team, including willing communication of adverse events (AEs), mental health history, current and past psychiatric medication \& treatments, and ability to...
- Participant agrees to provide emergency contact information at Screening Visit and their physical location at each visit (if they are joining the visit remotely).
- Participant is psychologically stable as determined by the investigator or delegate.
- Participant has access to the following:
- a device with stable internet and Wi-Fi connection capable of supporting video calls (e.g., tablet, computer with webcam, etc.)
- a second smart device that must be an iPhone 13 or newer (Not inclusive of the iPhone13 Mini)
- Participant home/environment meets criteria for Senseye DT setup (remote visits only)
What rules you out
- Current diagnosis of epilepsy and/or other seizure disorders.
- A history of at Screening OR positive at Visit 1 for bipolar I or II, mania, or one or more schizophrenia-spectrum or other psychotic disorders, including schizophrenia, schizoaffective disorder, delusional disorder...
- Compromised facial neuro-ophthalmic integrity (e.g., due to stroke, MS, ALS, or other neurological conditions).
- Current diagnosis of dementia, delirium, amnestic disorders, autism, hydrocephalus, posterior cortical atrophy, aphasia, multiple sclerosis, or stroke-related cognitive dysfunction.
- Current eye disorders which prevent the patient from using the Senseye DT:
- Vision impairment preventing ability to read with correction (including corneal disease, dense cataract, diabetic retinopathy, macular degeneration, glaucoma, etc.).
- Use of corrective lenses including glasses and contacts is permitted. Colored contacts and cosmetic lenses that obscure or enhance the pupil are not permitted.
- Significant eye lid droop blocking the pupil.
- Persistent blurry vision, headaches, and/or light sensitivity resulting from conditions including abnormal pupil dilation or reactivity (e.g, mydriasis).
- Recent eye surgeries (within 2 weeks) or planned eye surgeries within the study duration.
- Intraocular inflammation, including iritis and anterior uveitis.
- Ocular trauma resulting in uncorrected or permanent bilateral damage.
- Active suicidal and/or homicidal intent or other self-injurious behavior which may put the participant and/or others at risk per the investigator's clinical judgement, or has suicidal ideation of level 4 or 5 as...
- Suicidal behavior within the last year as determined by the C-SSRS at the time of screening.
- Significant suicidal ideation within the last 6 months as determined by ideation of level 4 or 5 by the C-SSRS at the time of screening.
- Current reported usage (within 2 weeks of Screening Visit and/or planned ongoing usage during the study) of psychotropic drugs and/or non-psychotropic drugs or medication which may affect use of the Senseye DT:
- Narcotics/opioids (e.g., Heroin, Vicodin, oxycodone, codeine, Tramadol, etc.).
- Tricyclic antidepressants (TCAs) (e.g., Tofranil, Pamelor, amitriptyline, doxeprin, etc.).
- Monoamine Oxidase Inhibitors (MAOIs) (e.g., Emsam, Parnate, Nardil, Marplan, etc.).
- Select antihypertensive medications (alpha-2 receptor agonists, clonidine, peripheral adrenergic inhibitors, Alpha \& Beta blockers, and Rauwolfia alkaloids). Note: If Prazosin can be abstained from for \> 24 hours...
- Psychedelics/psychotomimetics (Lysergic acid, psilocybin, mescaline, phencyclidine, methoxetamine, etc.).
- Cholinergic or anticholinergic agents (e.g., Urecholine, Pilocar, Aricept, Miostat, Evoxac, ipratropium/Atrovent, oxybutynin/Ditropan, scopolamine, etc.), except antihistamines other than Benadryl or diphenhydramine...
- Spravato or Ketamine.
- Eye drops unless the participant is able to abstain from use for \> 72 hours prior to the Senseye DT visit. Note: Artificial tears can be used if needed during the Senseye DT use.
- Central Nervous System (CNS) depressants (Benzodiazepines and Barbiturates)
- Current reported usage (within 2 weeks of Screening Visit and/or planned ongoing usage during the study) of vagal nerve stimulation, deep brain stimulation, transcranial magnetic stimulation, or other stimulation or...
- Any condition which precludes the ability for patients to safely and accurately complete clinical assessments, questionnaires, or to follow instructions necessary to administer the Senseye DT (e.g., significant...
- Medical diagnosis of Traumatic Brain Injury (TBI) within the last 12 months based on participant self-report.
- Lifetime history of any of the following: surgical procedures involving the brain or meninges, encephalitis, meningitis, degenerative central nervous system (CNS) disorder (e.g., Alzheimer's Disease, Parkinson's...
- Involved in active litigation related to the participant's psychiatric symptoms
- Pregnancy as determined by self-report.
- Currently incarcerated.
- Participant requires a legal authorized representative to consent.
- Prior enrollment in this study or in other Senseye Machine Learning (ML) studies within the last 12 months.
- Unwilling or unable to comply with all study related procedures, in the opinion of the investigator, including medical and non-medical procedures.
The study team makes the final eligibility decision.
Where it's taking place
- Aurora, Colorado, United States
- Savannah, Georgia, United States
- Meridian, Idaho, United States
- Boston, Massachusetts, United States
- Charleston, South Carolina, United States
- Carlton, Victoria, Australia
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Aurora, Colorado, United States; Savannah, Georgia, United States; Meridian, Idaho, United States; Boston, Massachusetts, United States; Charleston, South Carolina, United States; Carlton, Victoria, Australia. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.