Tulsa, OKNCT07710417Now EnrollingIRB Ready

Posttraumatic Stress Symptoms Clinical Trial in Tulsa, OK

Access cutting-edge posttraumatic stress symptoms treatment through this early phase 1 clinical trial at a research site in Tulsa. Study-provided care at no cost to qualified participants.

Sponsored by Laureate Institute for Brain Research, Inc.

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Expert Care in Tulsa

Access posttraumatic stress symptoms specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related posttraumatic stress symptoms treatment provided free

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Check if you qualify for this posttraumatic stress symptoms clinical trial in Tulsa, OK

Secure & Confidential

Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Tulsa

    Convenient for OK residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Tulsa site if eligible
  4. 4Begin participation

About This Posttraumatic Stress Symptoms Study in Tulsa

This early-stage pilot trial aims to examine the feasibility, tolerability, and safety of Floatation-REST, or Reduced Environmental Stimulation Therapy via floatation in frontline healthcare workers, first responders, and emergency medical personnel who experience post-traumatic stress symptoms.

Sponsor: Laureate Institute for Brain Research, Inc.

Who Can Participate

Inclusion Criteria

Work-related post-traumatic stress dysfunction as measured by either of the following inclusion pathways: (A) PTSS Pathway: PCL-5 greater than or equal to 20, OR meets criteria for full or partial PTSD on the MINI International Neuropsychiatric Interview 7 (DSM-V) (Criteria A + at least 2 B-E Criteria) OR (B) Functionally Anchored Pathway: evidence of work-related trauma exposure on the MINI International Neuropsychiatric Interview 7 (DSM-V) (Criterion A) or Life Events Checklist-5, and at least one of the following: Moral Injury and Distress Scale greater than or equal to 27, Sheehan Disability Scale greater than or equal to 5 on at least 1 of the 3 subscales, high or very high level of perceived stress (measured by PhenX Perceived Stress Scale greater than or equal to 16).
First responder or other emergency medical personnel
Ability to read, speak and understand English
Capable of providing consent

Exclusion Criteria

History of neurological conditions
Skin conditions or open wounds
DSM-5 diagnosis of psychotic spectrum disorders, obsessive-compulsive disorder, bipolar disorder, severe substance use disorder, or eating disorder
Inability to lay comfortably in a shallow pool of water
Failure to adhere to "pre-float checklist"
Breathalyzer test positive for alcohol or a drug-positive urine test
Unwillingness to provide consent or complete major aspects of protocol
MRI contraindications
Unstable medical diagnoses
Evidence of inability to comply with study procedures based on experimenter judgement
Change in the dose or prescription of a medication within the 6 weeks before enrolling in the study that could affect brain functioning (e.g., anxiolytics, antipsychotics, antidepressants, benzodiazepines, or mood stabilizers)

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Tulsa?

Yes, this clinical trial (NCT07710417) has an active research site in Tulsa, OK that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Posttraumatic Stress Symptoms Treatment Options in Tulsa, OK

If you're searching for posttraumatic stress symptoms treatment options in Tulsa, OK, this clinical trial (NCT07710417) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Tulsa research site is actively enrolling participants for this early phase 1 clinical trial. You'll receive care from experienced posttraumatic stress symptoms specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all posttraumatic stress symptoms clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Tulsa, OK