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NCT04132024 · ClinicalTrials.gov registry record · NA

Feasibility of Insomnia Tracking and Treatment in IBD

A NA study, sponsored by Dartmouth-Hitchcock Medical Center.

Completed
Registry status
NA
Development phase
39
Enrollment target

NCT04132024: Completed NA study, sponsored by Dartmouth-Hitchcock Medical Center.

NCT04132024 is a NA study that has completed, run by Dartmouth-Hitchcock Medical Center. The registered enrollment target is 39 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04132024, a NA study, has completed, sponsored by Dartmouth-Hitchcock Medical Center.

COMPLETED
Registry status
NA
Development phase
39 participants
Enrollment target

Study Summary

This study is a longitudinal clinical trial designed to characterize sleep patterns in individuals with Inflammatory Bowel Disease (IBD) as well as to assess the feasibility of sleep intervention (Cognitive Behavioral Therapy for Insomnia (CBT-I)) in individuals with both insomnia and Inflammatory Bowel Disease (IBD).

Primary Outcome

Sleep continuity will be measured by sleep onset latency (SOL), wake after sleep onset (WASO), total sleep time (TST), and sleep efficiency (SE), based on ActiGraph data and daily diary data. Sleep parameters measured by the ActiGraph model wGT3X-BT, a wrist-accelerometer. Measured in minutes of sleep per night. Higher number indicating longer sleep duration.

Interventions

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

Trial Details

FieldValue
Enrollment Target 39 participants
Start Date 2019-10-07
Est. Completion 2021-04-15
Phase NA
Dartmouth-Hitchcock Medical Center

427 total trials

What the finished NCT04132024 record still lists

NCT04132024 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 39 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).

The record links to 0 conditions, and to 1 intervention - of which Cognitive Behavioral Therapy for Insomnia (CBT-I) is the first listed.

NCT04132024 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04132024 about?

NCT04132024 is a clinical study titled "Feasibility of Insomnia Tracking and Treatment in IBD". This study is a longitudinal clinical trial designed to characterize sleep patterns in individuals with Inflammatory Bowel Disease (IBD) as well as to assess the feasibility of sleep intervention (Cognitive Behavioral Therapy for Insomnia (CBT-I)) in individuals with both insomnia and Inflammatory B...

What is the current status of trial NCT04132024?

This trial is currently completed. It is a NA study. The enrollment target is 39 participants. The study started on 2019-10-07. Estimated completion is 2021-04-15.

What interventions are being tested in trial NCT04132024?

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

Who is sponsoring clinical trial NCT04132024?

This trial is sponsored by Dartmouth-Hitchcock Medical Center, which has 427 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04132024's enrollment target sits among peer trials

39 1536th of 2000 higher than 463 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 NCT04132024, the US trial registry maintained by the National Library of Medicine. NCT04132024 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.