Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00152529 · ClinicalTrials.gov registry record

C.A.T.C.H.-I.T.Competent Adulthood Transition With Cognitive, Humanistic and Interpersonal Teaching

A clinical trial, sponsored by University of Chicago.

Terminated
Registry status
8
Enrollment target

NCT00152529: Clinical Trial study, sponsored by University of Chicago.

NCT00152529 is a clinical trial that was terminated before completion, run by University of Chicago. The registered enrollment target is 8 participants. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00152529 was terminated before completion, sponsored by University of Chicago.

TERMINATED
Registry status
8 participants
Enrollment target

Study Summary

The purpose of this study is to adapt depression prevention interventions of proven benefit to the primary care setting in a manner that would be acceptable and potentially available to young adults in the community.

Interventions

  • BEHAVIORAL Screening (Behavior)

Trial Details

FieldValue
Enrollment Target 8 participants
Start Date 2003-10
Est. Completion 2004-06
University of Chicago

796 total trials

Why NCT00152529 stopped before completion

NCT00152529 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 8 participants, a relatively small participant target.

The record links to 0 conditions, and to 1 intervention - of which Screening (Behavior) is the first listed.

NCT00152529 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00152529 about?

NCT00152529 is a clinical study titled "C.A.T.C.H.-I.T.Competent Adulthood Transition With Cognitive, Humanistic and Interpersonal Teaching". The purpose of this study is to adapt depression prevention interventions of proven benefit to the primary care setting in a manner that would be acceptable and potentially available to young adults in the community.

What is the current status of trial NCT00152529?

This trial is currently terminated. The enrollment target is 8 participants. The study started on 2003-10. Estimated completion is 2004-06.

What interventions are being tested in trial NCT00152529?

The interventions under investigation include: Screening (Behavior) (BEHAVIORAL).

Who is sponsoring clinical trial NCT00152529?

This trial is sponsored by University of Chicago, which has 796 total clinical trials registered on ClinicalTrials.gov.

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00152529, the US trial registry maintained by the National Library of Medicine. NCT00152529 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.