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NCT00127790 · ClinicalTrials.gov registry record · NA

Treatment of Insomnia Secondary to Chronic Pain

A NA study, sponsored by University of Rochester.

Completed
Registry status
NA
Development phase
28
Enrollment target

NCT00127790: Completed NA study, sponsored by University of Rochester.

NCT00127790 is a NA study that has completed, run by University of Rochester. The registered enrollment target is 28 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00127790, a NA study, has completed, sponsored by University of Rochester.

COMPLETED
Registry status
NA
Development phase
28 participants
Enrollment target

Study Summary

Several studies have shown that behavioral therapy for chronic pain can be beneficial for chronic pain and that behavioral therapy for insomnia can be beneficial for insomnia. However, seldom do chronic pain patients with insomnia receive a behavioral treatment for insomnia. The purpose of this study is to evaluate whether treatment for insomnia is helpful for pain and whether treatment for pain is helpful for insomnia. It will also assess whether a combined treatment is any more or less effective for pain or for sleep. Finally, the study will assess whether any of these treatments leads to improvements in immune function.

Primary Outcome

Total Score from the 7-item Insomnia Severity Index where total score ranges from 0-28 and higher scores indicate greater severity of insomnia.

Interventions

  • BEHAVIORAL CBT for Insomnia (CBT-I)
  • BEHAVIORAL CBT for Pain (CBT-P)

Trial Details

FieldValue
Enrollment Target 28 participants
Start Date 2005-06
Est. Completion 2008-11
Phase NA
University of Rochester

636 total trials

What the finished NCT00127790 record still lists

NCT00127790 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 28 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 2 interventions - of which CBT for Insomnia (CBT-I) is the first listed.

NCT00127790 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00127790 about?

NCT00127790 is a clinical study titled "Treatment of Insomnia Secondary to Chronic Pain". Several studies have shown that behavioral therapy for chronic pain can be beneficial for chronic pain and that behavioral therapy for insomnia can be beneficial for insomnia. However, seldom do chronic pain patients with insomnia receive a behavioral treatment for insomnia. The purpose of this stud...

What is the current status of trial NCT00127790?

This trial is currently completed. It is a NA study. The enrollment target is 28 participants. The study started on 2005-06. Estimated completion is 2008-11.

What interventions are being tested in trial NCT00127790?

The interventions under investigation include: CBT for Insomnia (CBT-I) (BEHAVIORAL), CBT for Pain (CBT-P) (BEHAVIORAL).

Who is sponsoring clinical trial NCT00127790?

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 NCT00127790's enrollment target sits among peer trials

28 1704th of 2000 higher than 293 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

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Source: ClinicalTrials.gov NCT00127790, the US trial registry maintained by the National Library of Medicine. NCT00127790 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.