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Recruiting NCT05800925

Triage Survey for Psychiatry Research Eligibility

Observational Major Depressive Disorder Borderline Personality Disorder Generalized Anxiety Disorder

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Survey.
Who it may be relevant to
Registry conditions: Major Depressive Disorder, Borderline Personality Disorder, Generalized Anxiety Disorder. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

TRIAGE-Psych is a survey study designed to assess potential participants' eligibility to screen for industry-sponsored psychiatry clinical trials.

Interventions

  • Other Survey
    Participants will be surveyed on demographics, medical history, and current psychiatric symptoms. Vital signs, urine drug screens, and urine pregnancy tests may be collected.

Primary outcome measures

  • The proportion of participants who are eligible for industry-sponsored clinical trials, as defined as those who go on to screen for a study [Time frame: Up to 52 weeks]
Secondary outcome measures (2)
  • The proportion of participants who enroll in industry-sponsored clinical trials [Time frame: Up to 52 weeks]
  • The prevalence of disqualifying comorbid conditions that prevent screening or enrollment in industry-sponsored clinical trials [Time frame: Up to 52 weeks]

Eligibility 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.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Case-only

Study locations

United States · 6 centers
  • Adams Clinical, Boston — Boston
  • Adams Clinical, Watertown — Watertown
  • Adams Clinical, Harlem — New York
  • Adams Clinical, Bronx — The Bronx
  • Adams Clinical, Philadelphia — Philadelphia
  • Adams Clinical, Dallas — DeSoto

Identifiers

NCT: NCT05800925 · TRIAGE-Psych-101

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗