New York, NYNCT06899165Now EnrollingIRB Ready

Psychological Stress Clinical Trial in New York, NY

Access cutting-edge psychological stress treatment through this phase 2 clinical trial at a research site in New York. Study-provided care at no cost to qualified participants.

Sponsored by Rachel Yehuda

Quick Self-Assessment

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Expert Care in New York

Access psychological stress specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related psychological stress treatment provided free

Apply for This New York Location

Check if you qualify for this psychological stress clinical trial in New York, NY

Secure & Confidential

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

Why Participate?

  • No-Cost Study Care

  • Local to New York

    Convenient for NY 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 New York site if eligible
  4. 4Begin participation

About This Psychological Stress Study in New York

This is an open-label psilocybin-assisted therapy study that will examine the safety and tolerability of psilocybin-assisted therapy in the offspring of genocide survivors with mood and anxiety disorders. The study will also investigate the efficacy of psilocybin-assisted therapy in reducing symptoms such as depression, anxiety and stress, as well as changes to the psychological effects of parental exposure to genocide, and changes to psychological resilience.

Sponsor: Rachel Yehuda

Who Can Participate

Inclusion Criteria

Age at least 18 years old at time of signing the informed consent
Biological child of at least one parent who directly survived/escaped a genocide
Meets diagnostic criteria for a depressive or anxiety disorder
Capable of providing informed consent and complying with study procedures
Currently using or agreeing to use adequate contraceptive methods.
Fluent in speaking and reading English
Able to swallow pills
Agrees to have study visits recorded with audio and video
Able to provide a contact person who can be reached by investigators in the event of the participant becoming unwell or unreachable
Agrees to inform the investigators within 48 hours of any medical conditions and procedures
Agrees to release of outside medical and psychiatric records
Must not participate in any other interventional clinical trials for the duration of the study.
Must commit to medication dosing, therapy, and all study procedures.

Exclusion Criteria

Not able to give adequate informed consent.
Was directly exposed to or survived a genocide.
Has a history of any medical condition, or any significant clinical finding on screening tests, that could make receiving psilocybin harmful.
Has acute, severe or unstable medical illness.
Has a history of stroke or Transient Ischemic Attack (TIA).
Has a history of psychiatric hospitalization within the last 6 months.
Current serious suicide risk.
Unable or unwilling to safely taper off prohibited psychiatric medications.
Abusing alcohol or other substances.
Has used psychedelics within 3 months of enrollment.
Are pregnant or nursing or able to become pregnant and are not practicing an effective means of contraception.

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 New York?

Yes, this clinical trial (NCT06899165) has an active research site in New York, NY 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.

Psychological Stress Treatment Options in New York, NY

If you're searching for psychological stress treatment options in New York, NY, this clinical trial (NCT06899165) 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 New York research site is actively enrolling participants for this phase 2 clinical trial. You'll receive care from experienced psychological stress 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 psychological stress clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · New York, NY