Ashtabula, OHNCT06018285Now EnrollingIRB Ready

Suicidal Ideation Clinical Trial in Ashtabula, OH

Access cutting-edge suicidal ideation treatment through this clinical trial at a research site in Ashtabula. Study-provided care at no cost to qualified participants.

Sponsored by Cynthia Fontanella

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Expert Care in Ashtabula

Access suicidal ideation specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related suicidal ideation treatment provided free

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Check if you qualify for this suicidal ideation clinical trial in Ashtabula, OH

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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 Ashtabula

    Convenient for OH 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 Ashtabula site if eligible
  4. 4Begin participation

About This Suicidal Ideation Study in Ashtabula

Suicide is the second leading cause of death among young people aged 12-17 years in the United States, yet many youth at risk for suicide are not identified or go untreated. Stepped care approaches have been shown to be effective at reducing suicide risk in clinical settings, including primary care. The goal of this hybrid I stepped wedge effectiveness-implementation study is to test the effectiveness of a population-based quality improvement (QI) intervention, entitled STARRS-PC (Stepped Approach to Reducing Risk of Suicide in Primary Care) compared to treatment as usual (TAU), in reducing the risk of suicidal behavior among youth in the pediatric primary care setting. STARRS-PC implements a clinical pathway for youth at elevated risk for suicide in pediatric primary care clinics. Clinical pathways are tools used by health professionals to guide evidence-informed practice. The STARRS-PC pathway consists of three evidence-based suicide clinical care processes: risk detection, assessment and triage, and, if needed, follow-up transitional care. STARRS-PC is guided by the Practical, Robust Implementation, and Sustainability Model (PRISM), which allows for the study of factors that influence effective implementation of the suicide prevention clinical pathway and is focused on scalability. The main questions the study aims to answer are: * Will STARRS-PC be more effective than TAU at reducing the rate of suicide attempt at 12 months post-baseline (primary outcome)? * Will STARRS-PC be more effective than TAU at reducing suicidal ideation and non-suicidal self-injury, and improving family satisfaction at 12 months post-baseline (secondary outcomes)? * What are the barriers and facilitators of effective implementation and sustainability of STARRS-PC?

Sponsor: Cynthia Fontanella

Who Can Participate

Inclusion Criteria

(Youth and Parent):
All patients between the ages of 12 - 17 years and their parent/guardian at time of consent who are identified as being at risk for suicide and receive primary care services at one of 14 participating sites are eligible for study inclusion.
Youth will be recruited without regard to current or past histories of mental health problems.
Youth with comorbid physical illness (e.g., asthma) and those receiving medication treatment for a comorbid physical or psychiatric condition will be eligible to participate provide they otherwise meet study entry criteria. Inclusion Criteria (Provider):
Providers must work with patients at one of the participating PCCs.

Exclusion Criteria

(Youth and Parent): Subjects will be excluded for being:
medically or cognitively unable to participate in study procedures
without permanent residence or access to a telephone
unable to speak English adequately to understand study procedures Exclusion Criteria (Provider):
Unable to give consent
Unable to speak English adequately to understand study procedures.

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 Ashtabula?

Yes, this clinical trial (NCT06018285) has an active research site in Ashtabula, OH 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.

Suicidal Ideation Treatment Options in Ashtabula, OH

If you're searching for suicidal ideation treatment options in Ashtabula, OH, this clinical trial (NCT06018285) 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 Ashtabula research site is actively enrolling participants for this clinical trial. You'll receive care from experienced suicidal ideation 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 suicidal ideation clinical trials near you to find additional studies recruiting in your area.

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