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Usefulness of a Telemedicine System for OSA Patients Follow-up With High Cardiovascular Risk (TELESAS)

Primary Purpose

Sleep Apnea, Obstructive, Obstructive Sleep Apnea Syndrome

Status
Terminated
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Telemedicine
Standard care
Sponsored by
Initiative Pour la Sante
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Sleep Apnea, Obstructive focused on measuring Obstructive Sleep Apnea Syndrome, SCORE, Telemedicine, Arterial blood pressure, Daily physical activity

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 18 to 85 years old men and women
  • stable patient
  • BMI<40kg/m²
  • OSA patients diagnosed with polysomnography or polygraphy
  • SCORE>5% and/or cardiovascular disease pas history :
  • transient ischemic attack, stroke, cerebral haemorrhagy
  • myocardial infraction, angor, coronary revascularization, arteriopathy, aortic aneurism

Exclusion Criteria:

  • central sleep apnea syndrome
  • SCORE<5%
  • cardiac failure
  • past history of hypercapnic chronic respiratory failure
  • past history of severe or intercurrent pathology which can not allow the patient follow-up
  • Incapacitated patients in accordance with article L 1121-6 of the public health code
  • patients taking part in another clinical trial

Sites / Locations

  • Liberal Office
  • Clermont Tonerre military hospital
  • Liberal Office
  • Liberal Office
  • University Hospital
  • Liberal Office
  • Liberal Office
  • Cornouaille Hospital
  • Montier Polyclinic
  • Hospitalor Hospital
  • Liberal Office
  • Liberal Office
  • Liberal Office
  • Liberal Office

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Telemedecine

Standard Care

Arm Description

CPAP treatment with telemedicine system

Standard care, including CPAP

Outcomes

Primary Outcome Measures

Home Arterial Blood Pressure
the primary outcome is assessed at weeks 1 and 16 for the both groups, moreover home arterial blood pressure is assessed each day, 2 times : morning and afternoon in the telemedicine group.
Home Arterial Blood Pressure
the primary outcome is assessed at weeks 1 and 16 for the both groups, moreover home arterial blood pressure is assessed each day, 2 times : morning and afternoon in the telemedicine group.

Secondary Outcome Measures

CPAP compliance
the CPAP compliance is assessed in the two groups at week 16
Sleepiness
Sleepiness is assessed with Epworth Sleepiness Scale at weeks 1 and 16 for the two groups
Physical Activity
Daily Physical Activity is assessed with an accelerometer (Sensewear Armband, Bodymedia) at weeks 1 and 16 in the two groups. Daily expenditure, steps number, daily METs are assessed.
Quality of Life
Quality of life is assessed with SF-12 questionnaire at weeks 1 and 16 in the two groups.
Cardiovascular risk SCORE
The cardiovascular risk SCORE is assessed at weeks 1 and 16 in the two groups.
Sleepiness
Sleepiness is assessed with Epworth Sleepiness Scale at weeks 1 and 16 for the two groups
Physical Activity
Daily Physical Activity is assessed with an accelerometer (Sensewear Armband, Bodymedia) at weeks 1 and 16 in the two groups. Daily expenditure, steps number, daily METs are assessed.
Quality of Life
Quality of life is assessed with SF-12 questionnaire at weeks 1 and 16 in the two groups.
Cardiovascular risk SCORE
The cardiovascular risk SCORE is assessed at weeks 1 and 16 in the two groups.

Full Information

First Posted
October 20, 2010
Last Updated
January 16, 2013
Sponsor
Initiative Pour la Sante
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1. Study Identification

Unique Protocol Identification Number
NCT01226641
Brief Title
Usefulness of a Telemedicine System for OSA Patients Follow-up With High Cardiovascular Risk
Acronym
TELESAS
Official Title
Usefulness of a Telemedicine System for OSA Patients Follow-up With High Cardiovascular Risk
Study Type
Interventional

2. Study Status

Record Verification Date
January 2013
Overall Recruitment Status
Terminated
Study Start Date
July 2009 (undefined)
Primary Completion Date
January 2012 (Actual)
Study Completion Date
January 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Initiative Pour la Sante

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The aim of this study is to determine the usefulness of a telemedicine system for the follow-up of OSA patients with a high cardiovascular risk. Our hypothesis is that the telemedicine system will enhance compliance and thus reduce self-measured blood pressure.
Detailed Description
The obstructive sleep apnea syndrome (OSAS) corresponds to repeated epochs of complete or incomplete pharynx collapses occurring during sleep. The Continuous Positive Airway Pressure is the gold standard treatment for OSAS. It consists of air insufflation in upper airways with a pressure of about 5 to 15 cm of water with a facial or nasal mask. CPAP treatment reduces cardiovascular morbi-mortality. OSAS is associated with cardiovascular mortality. A dose response effect exists between severity and arterial blood pressure. A recent meta-analysis has shown in unselected OSAS patients with or without hypertension, treated or non-treated for hypertension, CPAP reduces 24 h ambulatory blood pressure of approximately 2 mmHg. This decrease corresponds to a significant reduction in cardiovascular risk. The aim of the present study is to include OSAS patients with a high cardiovascular risk and to measure the effect of CPAP on home measurements of arterial blood pressure. This controlled randomized trial will compare the effect CPAP on arterial blood pressure in a group with a telemedicine system versus a group with standard home care CPAP treatment. An interim analysis will be carried out when 100 patients have been included in the study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sleep Apnea, Obstructive, Obstructive Sleep Apnea Syndrome
Keywords
Obstructive Sleep Apnea Syndrome, SCORE, Telemedicine, Arterial blood pressure, Daily physical activity

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
107 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Telemedecine
Arm Type
Experimental
Arm Description
CPAP treatment with telemedicine system
Arm Title
Standard Care
Arm Type
Active Comparator
Arm Description
Standard care, including CPAP
Intervention Type
Device
Intervention Name(s)
Telemedicine
Intervention Description
CPAP treatment with telemedicine system
Intervention Type
Device
Intervention Name(s)
Standard care
Intervention Description
Standard care, including CPAP
Primary Outcome Measure Information:
Title
Home Arterial Blood Pressure
Description
the primary outcome is assessed at weeks 1 and 16 for the both groups, moreover home arterial blood pressure is assessed each day, 2 times : morning and afternoon in the telemedicine group.
Time Frame
Home arterial Blood Pressure is assessed at week 1
Title
Home Arterial Blood Pressure
Description
the primary outcome is assessed at weeks 1 and 16 for the both groups, moreover home arterial blood pressure is assessed each day, 2 times : morning and afternoon in the telemedicine group.
Time Frame
Home arterial Blood Pressure is assessed at week 16
Secondary Outcome Measure Information:
Title
CPAP compliance
Description
the CPAP compliance is assessed in the two groups at week 16
Time Frame
week 16
Title
Sleepiness
Description
Sleepiness is assessed with Epworth Sleepiness Scale at weeks 1 and 16 for the two groups
Time Frame
weeks 1 and 16
Title
Physical Activity
Description
Daily Physical Activity is assessed with an accelerometer (Sensewear Armband, Bodymedia) at weeks 1 and 16 in the two groups. Daily expenditure, steps number, daily METs are assessed.
Time Frame
week 1
Title
Quality of Life
Description
Quality of life is assessed with SF-12 questionnaire at weeks 1 and 16 in the two groups.
Time Frame
week 16
Title
Cardiovascular risk SCORE
Description
The cardiovascular risk SCORE is assessed at weeks 1 and 16 in the two groups.
Time Frame
Week 1
Title
Sleepiness
Description
Sleepiness is assessed with Epworth Sleepiness Scale at weeks 1 and 16 for the two groups
Time Frame
week 16
Title
Physical Activity
Description
Daily Physical Activity is assessed with an accelerometer (Sensewear Armband, Bodymedia) at weeks 1 and 16 in the two groups. Daily expenditure, steps number, daily METs are assessed.
Time Frame
week 16
Title
Quality of Life
Description
Quality of life is assessed with SF-12 questionnaire at weeks 1 and 16 in the two groups.
Time Frame
week 1
Title
Cardiovascular risk SCORE
Description
The cardiovascular risk SCORE is assessed at weeks 1 and 16 in the two groups.
Time Frame
Week 16

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 18 to 85 years old men and women stable patient BMI<40kg/m² OSA patients diagnosed with polysomnography or polygraphy SCORE>5% and/or cardiovascular disease pas history : transient ischemic attack, stroke, cerebral haemorrhagy myocardial infraction, angor, coronary revascularization, arteriopathy, aortic aneurism Exclusion Criteria: central sleep apnea syndrome SCORE<5% cardiac failure past history of hypercapnic chronic respiratory failure past history of severe or intercurrent pathology which can not allow the patient follow-up Incapacitated patients in accordance with article L 1121-6 of the public health code patients taking part in another clinical trial
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean Louis PEPIN, Prof, PhD
Organizational Affiliation
University Hospital, Grenoble
Official's Role
Principal Investigator
Facility Information:
Facility Name
Liberal Office
City
Boulogne Billancourt
ZIP/Postal Code
92100
Country
France
Facility Name
Clermont Tonerre military hospital
City
Brest
ZIP/Postal Code
29200
Country
France
Facility Name
Liberal Office
City
Chambery
ZIP/Postal Code
73000
Country
France
Facility Name
Liberal Office
City
Grenoble
ZIP/Postal Code
38000
Country
France
Facility Name
University Hospital
City
Grenoble
ZIP/Postal Code
38000
Country
France
Facility Name
Liberal Office
City
Montigny les Metz
ZIP/Postal Code
57950
Country
France
Facility Name
Liberal Office
City
Nancy
ZIP/Postal Code
54000
Country
France
Facility Name
Cornouaille Hospital
City
Quimper
ZIP/Postal Code
29107
Country
France
Facility Name
Montier Polyclinic
City
St Andre les Vergers
ZIP/Postal Code
10120
Country
France
Facility Name
Hospitalor Hospital
City
St Avold
ZIP/Postal Code
57500
Country
France
Facility Name
Liberal Office
City
St Jean de Maurienne
ZIP/Postal Code
73300
Country
France
Facility Name
Liberal Office
City
St Martin les Boulogne
ZIP/Postal Code
62280
Country
France
Facility Name
Liberal Office
City
StIsmier
ZIP/Postal Code
38330
Country
France
Facility Name
Liberal Office
City
Strasbourg
ZIP/Postal Code
67000
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
25364081
Citation
Mendelson M, Vivodtzev I, Tamisier R, Laplaud D, Dias-Domingos S, Baguet JP, Moreau L, Koltes C, Chavez L, De Lamberterie G, Herengt F, Levy P, Flore P, Pepin JL. CPAP treatment supported by telemedicine does not improve blood pressure in high cardiovascular risk OSA patients: a randomized, controlled trial. Sleep. 2014 Nov 1;37(11):1863-70. doi: 10.5665/sleep.4186.
Results Reference
derived
PubMed Identifier
24282316
Citation
Mendelson M, Tamisier R, Laplaud D, Dias-Domingos S, Baguet JP, Moreau L, Koltes C, Chavez L, de Lamberterie G, Herengt F, Levy P, Flore P, Pepin JL. Low physical activity is a determinant for elevated blood pressure in high cardiovascular risk obstructive sleep apnea. Respir Care. 2014 Aug;59(8):1218-27. doi: 10.4187/respcare.02948.
Results Reference
derived

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Usefulness of a Telemedicine System for OSA Patients Follow-up With High Cardiovascular Risk

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