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

NCT00895999 · ClinicalTrials.gov registry record · NA

Psychosocial Treatment for Women With Depression and Pain

A NA study, sponsored by University of Rochester.

Completed
Registry status
NA
Development phase
60
Enrollment target

NCT00895999: Completed NA study, sponsored by University of Rochester.

NCT00895999 is a NA study that has completed, run by University of Rochester. The registered enrollment target is 60 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00895999, a NA study, has completed, sponsored by University of Rochester.

COMPLETED
Registry status
NA
Development phase
60 participants
Enrollment target

Study Summary

Patients with depression and pain have poorer outcomes in response to depression treatments than depressed patients without pain. While psychotherapy treatment studies have demonstrated improvement in pain and depression, no psychosocial interventions have been developed and tested prospectively specifically for patients with both conditions. Interpersonal psychotherapy (IPT), an effective treatment for depression, has been adapted successfully for physically ill patients and demonstrates good adherence, treatment satisfaction, and depression outcomes. The investigators propose to test a modified form of IPT-P for depressed patients with co-morbid pain.

Interventions

  • BEHAVIORAL Interpersonal Therapy for Pain (IPT-P)
  • BEHAVIORAL Enhanced Support and Connection to Counseling

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2007-03
Est. Completion 2011-12
Phase NA
University of Rochester

636 total trials

What the finished NCT00895999 record still lists

NCT00895999 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 60 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 2 interventions - of which Interpersonal Therapy for Pain (IPT-P) is the first listed.

NCT00895999 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00895999 about?

NCT00895999 is a clinical study titled "Psychosocial Treatment for Women With Depression and Pain". Patients with depression and pain have poorer outcomes in response to depression treatments than depressed patients without pain. While psychotherapy treatment studies have demonstrated improvement in pain and depression, no psychosocial interventions have been developed and tested prospectively spe...

What is the current status of trial NCT00895999?

This trial is currently completed. It is a NA study. The enrollment target is 60 participants. The study started on 2007-03. Estimated completion is 2011-12.

What interventions are being tested in trial NCT00895999?

The interventions under investigation include: Interpersonal Therapy for Pain (IPT-P) (BEHAVIORAL), Enhanced Support and Connection to Counseling (BEHAVIORAL).

Who is sponsoring clinical trial NCT00895999?

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

How this trial's enrollment target compares

Where NCT00895999's enrollment target sits among peer trials

60 1164th of 2000 higher than 745 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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

  • NCT00576069 · 60 participants

    Mechanism(s)of Airflow Limitation in Moderate-severe Persistent Asthma

  • NCT01297400 · 60 participants · Phase 2

    Phase 2 Pilot Study of the Safety and Efficacy of Topical MW-III in Thermal Burns

  • NCT01734122 · 60 participants

    Stereotactic Radiosurgery for Essential Tremor and Parkinsonian Tremor

  • NCT01804634 · 60 participants · Phase 2

    Reduced Intensity Haploidentical BMT for High Risk Solid Tumors

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 NCT00895999, the US trial registry maintained by the National Library of Medicine. NCT00895999 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.