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NCT02001077 · ClinicalTrials.gov registry record · NA

Sleep and Pain Interventions in Fibromyalgia

A NA study, sponsored by University of Florida.

Completed
Registry status
NA
Development phase
113
Enrollment target

NCT02001077: Completed NA study, sponsored by University of Florida.

NCT02001077 is a NA study that has completed, run by University of Florida. The registered enrollment target is 113 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02001077, a NA study, has completed, sponsored by University of Florida.

COMPLETED
Registry status
NA
Development phase
113 participants
Enrollment target

Study Summary

This is a single-center, randomized controlled trial study design. Enrolled participants had comorbid fibromyalgia and chronic insomnia. Participants were randomized to a behavioral intervention for pain, a behavioral intervention for insomnia, or a waitlist control. The study intervention period lasted eight weeks. The objective of the study is to examine the impact of two behavioral treatments on sleep and pain and to better understand what causes chronic pain and chronic sleep disturbance.

Primary Outcome

The change in the time participants report spending awake during the night. Sleep will be measured with daily diaries and, means of the 14 days collected at baseline, immediately, and 6 months following treatment will be calculated.

Interventions

  • BEHAVIORAL Cognitive Behavioral Therapy for Insomnia (CBT-I)
  • BEHAVIORAL Cognitive Behavioral Therapy for Pain (CBT-P)

Trial Details

FieldValue
Enrollment Target 113 participants
Start Date 2009-02
Est. Completion 2013-09
Phase NA
University of Florida

1,106 total trials

What the finished NCT02001077 record still lists

NCT02001077 is an interventional study that assigns participants to a tested intervention. The registered 113 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower).

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

NCT02001077 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02001077 about?

NCT02001077 is a clinical study titled "Sleep and Pain Interventions in Fibromyalgia". This is a single-center, randomized controlled trial study design. Enrolled participants had comorbid fibromyalgia and chronic insomnia. Participants were randomized to a behavioral intervention for pain, a behavioral intervention for insomnia, or a waitlist control. The study intervention period la...

What is the current status of trial NCT02001077?

This trial is currently completed. It is a NA study. The enrollment target is 113 participants. The study started on 2009-02. Estimated completion is 2013-09.

What interventions are being tested in trial NCT02001077?

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

Who is sponsoring clinical trial NCT02001077?

This trial is sponsored by University of Florida, which has 1,106 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02001077's enrollment target sits among peer trials

113 813th of 2000 higher than 1,188 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 NCT02001077, the US trial registry maintained by the National Library of Medicine. NCT02001077 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.