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NCT01678560 · ClinicalTrials.gov registry record · NA

Remote Monitoring in Obstructive Sleep Apnea

A NA study, sponsored by VA Connecticut Healthcare System.

Terminated
Registry status
NA
Development phase
52
Enrollment target

NCT01678560: Clinical Trial NA study, sponsored by VA Connecticut Healthcare System.

NCT01678560 is a NA study that was terminated before completion, run by VA Connecticut Healthcare System. The registered enrollment target is 52 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01678560, a NA study, was terminated before completion, sponsored by VA Connecticut Healthcare System.

TERMINATED
Registry status
NA
Development phase
52 participants
Enrollment target

Study Summary

Obstructive sleep apnea (OSA) among Veterans is a condition that imparts a great burden to the patient in terms of serious co-morbidities and results in a great cost to the VA Health Care System to treat the co-morbidities, which include heart disease, stroke and neuropsychiatric disorders. Positive airway pressure (PAP) is used to treat sleep apnea and studies have shown a poor adherence to treatment. The investigators hypothesize that using wireless technology will lead to early detection of problems of treatment use and will translate into early remedial action which will improve the use and effectiveness of treatment. The investigators will compare two methods. Usual care involves downloading data from PAP machines at designated 3-month intervals, requiring a face-to-face clinician visit. Wireless care involved more frequent monitoring and intervention in the event of anomalies in treatment use or effectiveness.

Interventions

  • DEVICE Monitoring every 3 months by face-to-face visits
  • DEVICE Frequent remote monitoring

Trial Details

FieldValue
Enrollment Target 52 participants
Start Date 2014-01
Est. Completion 2016-12
Phase NA

Sponsor

VA Connecticut Healthcare System

26 total trials

What the Registry Record Tells You About NCT01678560

The ClinicalTrials.gov registry entry for NCT01678560 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 52 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is VA Connecticut Healthcare System, which has 26 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Monitoring every 3 months by face-to-face visits is the first listed.

NCT01678560 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01678560 about?

NCT01678560 is a clinical study titled "Remote Monitoring in Obstructive Sleep Apnea". Obstructive sleep apnea (OSA) among Veterans is a condition that imparts a great burden to the patient in terms of serious co-morbidities and results in a great cost to the VA Health Care System to treat the co-morbidities, which include heart disease, stroke and neuropsychiatric disorders. Positive...

What is the current status of trial NCT01678560?

This trial is currently terminated. It is a NA study. The enrollment target is 52 participants. The study started on 2014-01. Estimated completion is 2016-12.

What interventions are being tested in trial NCT01678560?

The interventions under investigation include: Monitoring every 3 months by face-to-face visits (DEVICE), Frequent remote monitoring (DEVICE).

Who is sponsoring clinical trial NCT01678560?

This trial is sponsored by VA Connecticut Healthcare System, which has 26 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, the data changelog, or report a data error.