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Validation of Safety and Efficacy for Night Shift Therapy

NCT02032706 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 36

Last updated 2016-04-01

Study results available
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Summary

The purpose of this study is to assess the accuracy of Night Shift in the detection of supine sleep and efficacy of vibro-tactile feedback in restricting supine sleep.

Conditions

Interventions

DEVICE

Deliver therapy when the supine position is detected

Application of vibrotactile feedback to the neck when the supine position is detected

Sponsors & Collaborators

  • Advanced Brain Monitoring, Inc.

    lead INDUSTRY

Principal Investigators

  • Daniel J Levendowski, MBA · Advanced Brain Monitoring, Inc.

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-06-30
Primary Completion
2014-02-28
Completion
2014-02-28

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02032706 on ClinicalTrials.gov