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NCT06060158 · ClinicalTrials.gov registry record · NA

Feasibility of Internet Group CBT-I for Gyn Oncology Patients

A NA study, sponsored by University of California, Davis.

Completed
Registry status
NA
Development phase
5
Enrollment target

NCT06060158: Completed NA study, sponsored by University of California, Davis.

NCT06060158 is a NA study that has completed, run by University of California, Davis. The registered enrollment target is 5 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06060158, a NA study, has completed, sponsored by University of California, Davis.

COMPLETED
Registry status
NA
Development phase
5 participants
Enrollment target

Study Summary

The goal of this study is to evaluate the feasibility and acceptability of delivering cognitive behavioral therapy for insomnia (CBT-I) to gynecologic cancer patients in an internet-based small-group setting. Secondary objectives: 1. To compare insomnia symptoms before and after intervention. 2. To evaluate any changes in quality of life symptoms while undergoing the intervention. 3. To evaluate the duration of symptoms improvement after the intervention is complete.

Primary Outcome

Main feasibility metric, recorded as number of sessions successfully attended. Participants would need to attend at least 4 sessions of the CBT-I sessions. Therefore, attendance among all participants must be 67% or greater to be considered feasible. A session must be attended for at least 50% of the time or will be counted as missed.

Interventions

  • BEHAVIORAL Cognitive Behavioral Therapy for Insomnia

Trial Details

FieldValue
Enrollment Target 5 participants
Start Date 2024-02-26
Est. Completion 2024-12-10
Phase NA
University of California, Davis

657 total trials

What the finished NCT06060158 record still lists

NCT06060158 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 5 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower).

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

NCT06060158 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06060158 about?

NCT06060158 is a clinical study titled "Feasibility of Internet Group CBT-I for Gyn Oncology Patients". The goal of this study is to evaluate the feasibility and acceptability of delivering cognitive behavioral therapy for insomnia (CBT-I) to gynecologic cancer patients in an internet-based small-group setting. Secondary objectives: 1. To compare insomnia symptoms before and after intervention. 2. T...

What is the current status of trial NCT06060158?

This trial is currently completed. It is a NA study. The enrollment target is 5 participants. The study started on 2024-02-26. Estimated completion is 2024-12-10.

What interventions are being tested in trial NCT06060158?

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

Who is sponsoring clinical trial NCT06060158?

This trial is sponsored by University of California, Davis, which has 657 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06060158's enrollment target sits among peer trials

5 1988th of 2000 higher than 5 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 NCT06060158, the US trial registry maintained by the National Library of Medicine. NCT06060158 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.