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

NCT00257400 · ClinicalTrials.gov registry record · Phase 1

Comparison of Two Psychotherapy Treatments for Depressed Women With a History of Sexual Abuse

A Phase 1 study of Depression, sponsored by University of Rochester.

Completed
Registry status
Phase 1
Development phase
70
Enrollment target
1
Study location

NCT00257400: Completed Phase 1 study of Depression, sponsored by University of Rochester.

NCT00257400 is a Phase 1 study of Depression that has completed, run by University of Rochester. The registered enrollment target is 70 participants, below the 786-participant average among 679 other Depression trials with a reported enrollment target (91% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00257400, a Phase 1 study of Depression, has completed, sponsored by University of Rochester.

COMPLETED
Registry status
Phase 1
Development phase
70 participants
Enrollment target
1
Study location

Study Summary

This study will compare the effectiveness of individual versus interpersonal psychotherapy in treating depressed women with a history of sexual abuse.

Conditions Studied

Interventions

  • BEHAVIORAL Interpersonal Psychotherapy (IPT)
  • BEHAVIORAL Individual Psychotherapy

Study Locations (1)

New York

  • University of Rochester Medical Center - Rochester

Trial Details

FieldValue
Enrollment Target 70 participants
Start Date 2003-05
Est. Completion 2007-08
Phase Phase 1
University of Rochester

636 total trials

What the finished NCT00257400 record still lists

NCT00257400 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 70 participants, a relatively small participant target, below the 786-participant average among 679 other Depression trials with a reported enrollment target (91% lower).

The record links to 1 condition, with Depression appearing as the primary indexed condition, and to 2 interventions - of which Interpersonal Psychotherapy (IPT) is the first listed.

NCT00257400 reports a single indexed study location in New York.

Frequently Asked Questions

What is clinical trial NCT00257400 about?

NCT00257400 is a clinical study titled "Comparison of Two Psychotherapy Treatments for Depressed Women With a History of Sexual Abuse". This study will compare the effectiveness of individual versus interpersonal psychotherapy in treating depressed women with a history of sexual abuse.

What is the current status of trial NCT00257400?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 70 participants. The study started on 2003-05. Estimated completion is 2007-08.

What conditions does trial NCT00257400 study?

This clinical trial studies the following conditions: Depression.

What interventions are being tested in trial NCT00257400?

The interventions under investigation include: Interpersonal Psychotherapy (IPT) (BEHAVIORAL), Individual Psychotherapy (BEHAVIORAL).

Who is sponsoring clinical trial NCT00257400?

This trial is sponsored by University of Rochester, which has 636 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00257400 being conducted?

This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Depression

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT00257400's enrollment target sits among peer trials

70 407th of 679 higher than 266 of 679 other Depression trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Depression trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

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

Similar enrollment target

  • NCT00969111 · 70 participants · NA

    Postoperative or Salvage Radiotherapy (RT) for Node Negative Prostate Cancer Following Radical Prostatectomy

  • NCT01712620 · 70 participants · Phase 2

    Spironolactone for Pulmonary Arterial Hypertension

  • NCT02143830 · 70 participants · Phase 2

    HSCT for Patients With Fanconi Anemia Using Risk-Adjusted Chemotherapy

  • NCT02601339 · 70 participants

    NIRS Monitoring in Premature Infants

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 NCT00257400, the US trial registry maintained by the National Library of Medicine. NCT00257400 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.