Recruiting NCT05800925
Triage Survey for Psychiatry Research Eligibility
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 →
Unsure about the terms? Read our patient guide →
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