NCT05800925

Brief Summary

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

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
20,000

participants targeted

Target at P75+ for all trials

Timeline
18mo left

Started Dec 2021

Longer than P75 for all trials

Geographic Reach
1 country

6 active sites

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress74%
Dec 2021Dec 2027

Study Start

First participant enrolled

December 21, 2021

Completed
1.3 years until next milestone

First Submitted

Initial submission to the registry

March 24, 2023

Completed
13 days until next milestone

First Posted

Study publicly available on registry

April 6, 2023

Completed
4.7 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2027

Last Updated

May 20, 2026

Status Verified

May 1, 2026

Enrollment Period

6 years

First QC Date

March 24, 2023

Last Update Submit

May 18, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • The proportion of participants who are eligible for industry-sponsored clinical trials, as defined as those who go on to screen for a study

    Up to 52 weeks

Secondary Outcomes (2)

  • The proportion of participants who enroll in industry-sponsored clinical trials

    Up to 52 weeks

  • The prevalence of disqualifying comorbid conditions that prevent screening or enrollment in industry-sponsored clinical trials

    Up to 52 weeks

Interventions

SurveyOTHER

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

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Participants of any sex, age 18+, who have expressed interest in participating in an industry-sponsored clinical trial of an investigational product for indications in psychiatry will be screened for clinical appropriateness for a study trial.

You may qualify if:

  • Participant or Legally Authorized Representative has signed an ICF prior to study-specific procedures being performed.
  • Participant is at least 18 years old.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (6)

Adams Clinical, Boston

Boston, Massachusetts, 02116, United States

RECRUITING

Adams Clinical, Watertown

Watertown, Massachusetts, 02472, United States

RECRUITING

Adams Clinical, Harlem

New York, New York, 10029, United States

RECRUITING

Adams Clinical, Bronx

The Bronx, New York, 10461, United States

RECRUITING

Adams Clinical, Philadelphia

Philadelphia, Pennsylvania, 19104, United States

RECRUITING

Adams Clinical, Dallas

DeSoto, Texas, 75115, United States

RECRUITING

MeSH Terms

Conditions

Depressive Disorder, MajorBorderline Personality DisorderGeneralized Anxiety Disorder

Interventions

Surveys and Questionnaires

Condition Hierarchy (Ancestors)

Depressive DisorderMood DisordersMental DisordersPersonality DisordersAnxiety Disorders

Intervention Hierarchy (Ancestors)

Data CollectionEpidemiologic MethodsInvestigative TechniquesHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public Health

Central Study Contacts

Miriam Evans, PhD

CONTACT

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
PROSPECTIVE
Sponsor Type
NETWORK
Responsible Party
SPONSOR

Study Record Dates

First Submitted

March 24, 2023

First Posted

April 6, 2023

Study Start

December 21, 2021

Primary Completion (Estimated)

December 31, 2027

Study Completion (Estimated)

December 31, 2027

Last Updated

May 20, 2026

Record last verified: 2026-05

Locations