San Francisco, CANCT07511088Now EnrollingIRB Ready

Situational Anxiety Clinical Trial in San Francisco, CA

Access cutting-edge situational anxiety treatment through this clinical trial at a research site in San Francisco. Study-provided care at no cost to qualified participants.

Sponsored by PLT Health Solutions

Quick Self-Assessment

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Expert Care in San Francisco

Access situational anxiety specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related situational anxiety treatment provided free

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Check if you qualify for this situational anxiety clinical trial in San Francisco, CA

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

Why Participate?

  • No-Cost Study Care

  • Local to San Francisco

    Convenient for CA 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 San Francisco site if eligible
  4. 4Begin participation

About This Situational Anxiety Study in San Francisco

The purpose of this decentralized, two-arm, double-blinded, crossover clinical study is to test the efficacy of a supplement to reduce symptoms of acute stress or situational anxiety in healthy volunteers. The main questions it aims to answer are: 1. Does a dietary supplement reduce feelings of anxiety after self-identified episodes of stress or anxiety when compared to their experience after taking a placebo? 2. On a scale of 1-5, how much would the volunteer like to take the assigned treatment in the future? 3. Are any adverse events identified after either treatment, supplement, or placebo? The study volunteers will: During weeks 1-2, self-identify episodes of acute stress or situational anxiety and rate feelings of anxiety over the next five hours after taking the study product assigned for Period 1. During week 3, volunteers will not take any study product nor complete any surveys. During weeks 4-5, self-identify an episode of acute stress or situational anxiety and rate feelings of anxiety over the next five hours after taking the study product assigned for Period 2.

Sponsor: PLT Health Solutions

Who Can Participate

Inclusion Criteria

Female and male subjects aged \>18 and \<60 years.
Self-reported experience of episodic stress or situational anxiety of ≥1 x per week.
Score of ≥ 40 on a self-assessment of typical anxiety on a Visual Analog Scale where 0 represents "not stressed or anxious" and 100 represents "extremely stressed or anxious."
Score of ≥ 20 on the Positive Reactivity component of the Perth Emotional Reactivity Scale- Short Form (PERS-S).
Ability to complete surveys on the Alethios digital platform.
Subject is only taking well-established, stable doses of prescription and non-prescription medications that are not indicated to treat anxiety disorder.
Subject is in generally good health as determined by a review of self-reported medical history and in the opinion of the Principal Investigator.
Women of child-bearing potential must agree to use a medically approved form of birth control during the study. Acceptable methods of birth control include hormonal - oral (pill), implantable, injectable (shot), ring, or transdermal (patch) contraceptives; mechanical - spermicide in conjunction with a barrier such as a diaphragm or condom; or an intra-uterine device (IUD.
Subject agrees to abstain from cannabis use for the duration of the study period
Subject agrees to maintain current dietary habits and abstain from using dietary supplements or herbal products thought to affect a sense of calming, including ashwagandha, L-theanine, or St. John's Wort, for the duration of the study period.
Individual is aware of the procedures and agrees to participate in the study.
Participant understands and is willing to sign an Informed eConsent in conformance with 21 CFR Part 50: "Protection of Human Participants."

Exclusion Criteria

Score of \> 9 on the Patient Health Questionnaire (PHQ-9) or any response \> 0 on question 9 of the PHQ-9.
Score \> 24 on the Hamilton Anxiety Scale (HAM-A).
History of severe psychiatric or medical conditions that would interfere with participation.
Use of \>14 alcoholic drinks per week.
Subject is a regular cannabis user, as defined as equal to or greater than 2 times per week over the prior 6 weeks.
Individuals with a history of drug abuse or dependence within the past 6 months.
Changes to medication treatment for any health condition within the prior 3 months.
Use of any prescription medication for anxiety.
Any diagnosis of a mental health condition in the prior 3 months.
Unstable medical conditions.
Known hypersensitivity to study product.
Participant is pregnant, planning to become pregnant, or breastfeeding.
Pregnant or lactating women or women of child-bearing potential unwilling to use a medically approved form of birth control.
Inability to comply with digital study requirements.
Participation in a clinical study within 30 days prior to randomization

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 San Francisco?

Yes, this clinical trial (NCT07511088) has an active research site in San Francisco, CA 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.

Situational Anxiety Treatment Options in San Francisco, CA

If you're searching for situational anxiety treatment options in San Francisco, CA, this clinical trial (NCT07511088) 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 San Francisco research site is actively enrolling participants for this clinical trial. You'll receive care from experienced situational anxiety 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 situational anxiety clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · San Francisco, CA