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NCT05875129 · ClinicalTrials.gov registry record · NA

Device Feasibility and Acceptability to Improve Insomnia in Cancer

A NA study, sponsored by Medstar Health Research Institute.

Completed
Registry status
NA
Development phase
15
Enrollment target

NCT05875129: Completed NA study, sponsored by Medstar Health Research Institute.

NCT05875129 is a NA study that has completed, run by Medstar Health Research Institute. The registered enrollment target is 15 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05875129, a NA study, has completed, sponsored by Medstar Health Research Institute.

COMPLETED
Registry status
NA
Development phase
15 participants
Enrollment target

Study Summary

Sleep disruption is common among young adult cancer survivors for a variety of reasons. Cognitive behavioral therapy for insomnia (CBT-I) has been shown to improve chronic sleep disorders. This project will test the feasibility and acceptability of a new voice-activated virtual assistant (VAVA) device to deliver CBT-I to improve sleep among young adult cancer survivors with chronic sleep disorders.

Primary Outcome

Number of days that a participant interacted with the VAVA

Interventions

  • DEVICE VAVA prototype

Trial Details

FieldValue
Enrollment Target 15 participants
Start Date 2022-07-20
Est. Completion 2023-12-31
Phase NA
Medstar Health Research Institute

115 total trials

What the finished NCT05875129 record still lists

NCT05875129 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 15 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 1 intervention - of which VAVA prototype is the first listed.

NCT05875129 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05875129 about?

NCT05875129 is a clinical study titled "Device Feasibility and Acceptability to Improve Insomnia in Cancer". Sleep disruption is common among young adult cancer survivors for a variety of reasons. Cognitive behavioral therapy for insomnia (CBT-I) has been shown to improve chronic sleep disorders. This project will test the feasibility and acceptability of a new voice-activated virtual assistant (VAVA) devi...

What is the current status of trial NCT05875129?

This trial is currently completed. It is a NA study. The enrollment target is 15 participants. The study started on 2022-07-20. Estimated completion is 2023-12-31.

What interventions are being tested in trial NCT05875129?

The interventions under investigation include: VAVA prototype (DEVICE).

Who is sponsoring clinical trial NCT05875129?

This trial is sponsored by Medstar Health Research Institute, which has 115 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05875129's enrollment target sits among peer trials

15 1881st of 2000 higher than 92 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 NCT05875129, the US trial registry maintained by the National Library of Medicine. NCT05875129 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.