Efficacy and Safety of the Device Siesta-SystemTM for Inducing Objective Sleep and re Rest

Sponsor
Basque Health Service (Other)
Overall Status
Completed
CT.gov ID
NCT01062295
Collaborator
(none)
40
1
2
15
2.7

Study Details

Study Description

Brief Summary

NTRODUCTION: The investigators have developed a new device to help passengers of vehicles to rest, sleep, and to avoid cervical injuries due to sleepiness postures while travelling. The device is attached to the headrest and is based in a new concept called "dynamic vertical holding of the head and neck". It could also provide some help in avoiding accidents by allowing a sleeping time for a secondary driver while the main one is driving. Several studies have shown that up to 30% of car crashes are related to sleepiness.

AIM: To estimate the efficacy and safety of a new device in "patent pending" phase to facilitate the sleep and rest in the passenger.

METODOLOGY: DESIGN: Prospective, cross-over and open clinical assay, comparing the results of 40 different passengers during a journey after using both systems, that is the new device and the standard headrest.

MEASUREMENTS: A) Standard polysomnography for 3 and a half hours during the night; B) Anthropometric and clinical variables; C) Sleepiness scale and Epworth sleepiness; D) Questionnaires of sleep, health and quality of life. E) Evaluation of the neck posture in recorded images.

ANALYSIS: To compare the results of questionnaires of sleep quality, comfort and safety as well as the images recorded and polysomnographic variables of objective sleep variables obtained by the device Siesta-SystemTM and the conventional headrest.

Condition or Disease Intervention/Treatment Phase
  • Device: Siesta-System
  • Device: Standard headrest
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
40 participants
Intervention Model:
Crossover Assignment
Primary Purpose:
Supportive Care
Official Title:
Efficacy and Safety of the Device Siesta-SystemTM for Inducing Objective Sleep and re Rest.
Study Start Date :
Nov 1, 2008
Actual Primary Completion Date :
May 1, 2009
Actual Study Completion Date :
Feb 1, 2010

Arms and Interventions

Arm Intervention/Treatment
Experimental: Siesta-System

Use of Siesta-System

Device: Siesta-System

Active Comparator: Standard headrest

Use of standard headrest

Device: Standard headrest

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    30 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Adults between 30 and 80 years
    Exclusion Criteria:
    • People with back pain or hip area on trips of 5 hours. Acute passenger. Serious chronic illness. Depressions. Medicated people with sleep inducing drugs or stimulants. People with insomnia relevant and apnea-hypopnea syndrome during sleep (SAHS) will be excluded by validated sleep test. People who have drunk in the last 6 hours coffee, other drinks, exciting, or an amount of alcohol over a glass of wine and those who stayed more than 30 minutes las12 hours before the test. People who declare themselves unable to relax in a vehicle while riding as co-pilots. Morbid obesity (BMI> 40 kg/m2) and any musculoskeletal disorder defined as a disease that can trouble the rest and sleep onset in a car. Latex allergy.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Txagorritxu Hospital Vitoria-Gasteiz Alava Spain 01009

    Sponsors and Collaborators

    • Basque Health Service

    Investigators

    • Principal Investigator: Joaquin DurĂ¡n-Cantolla, MD, PhD, Osakidetza/ Basque Health System

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT01062295
    Other Study ID Numbers:
    • conductores
    First Posted:
    Feb 4, 2010
    Last Update Posted:
    Feb 4, 2010
    Last Verified:
    Oct 1, 2009
    Keywords provided by , ,

    Study Results

    No Results Posted as of Feb 4, 2010