Survey to determine eligibility for psychiatry clinical trials
Triage Survey for Psychiatry Research Eligibility
This study is trying to see if people with conditions like depression, anxiety, or personality disorders can join upcoming psychiatry clinical trials.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 2000 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Adams Clinical Research network |
| Locations | 3 sites (Boston, Massachusetts and 2 other locations) |
| Trial ID | NCT05800925 on ClinicalTrials.gov |
What this trial studies
TRIAGE-Psych is an observational survey designed to evaluate potential participants' eligibility for industry-sponsored clinical trials in psychiatry. The study focuses on individuals with conditions such as Major Depressive Disorder, Borderline Personality Disorder, and Generalized Anxiety Disorder. Participants must be at least 18 years old and provide informed consent before participating. The survey aims to streamline the recruitment process for future clinical trials by identifying suitable candidates.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 and older who are experiencing major depressive disorder, borderline personality disorder, or generalized anxiety disorder.
Not a fit: Patients who are pregnant, breastfeeding, or at acute suicidal risk may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance the recruitment process for clinical trials, leading to more effective treatments for psychiatric conditions.
How similar studies have performed: While this approach is primarily observational and focused on eligibility screening, similar studies have successfully streamlined participant recruitment in clinical trials.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Participant or Legally Authorized Representative has signed an ICF prior to study-specific procedures being performed. * Participant is at least 18 years old. Exclusion Criteria: * Participant is pregnant, breast-feeding, or planning to become pregnant. * History of a clinically significant illness which in the investigator's opinion may impact participant safety or the ability to analyze study results. * Participant represents an acute suicidal risk, as defined as a "yes" response to ideation on C-SSRS questions 4 or 5, or answer "yes" to behavior questions within 90 days of screening. * Moderate or severe substance use disorder within 90 days prior to screen, according to DSM-5 criteria that in the investigator's opinion could pose undue risk to the participant. * Any condition that in the investigator's opinion makes a participant unsuitable for the study. * Currently employed by Adams Clinical or a first-degree relative of an employee.
Where this trial is running
Boston, Massachusetts and 2 other locations
- Copley Clinical — Boston, Massachusetts, United States (Recruiting)
- Adams Clinical — Watertown, Massachusetts, United States (Recruiting)
- Berman Clinical — New York, New York, United States (Recruiting)
Study contacts
- Study coordinator: Miriam Evans, PhD
- Email: mevans@adamsclinical.com
- Phone: 617-744-8542
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.