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Physical Activity Program for Reducing Blood Pressure in Sleep Apnea Patients With Resistant Hypertension (RAP)

Primary Purpose

Hypertension, Resistant to Conventional Therapy, Sleep Apnea

Status
Unknown status
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Physical activity
Sponsored by
AGIR à Dom
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hypertension, Resistant to Conventional Therapy

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Patient with an obstructive sleep apnea (apnea-hypopnea index > or equal to 15)
  • Patient with resistant hypertension uncontrolled by 3 or more antihypertensive agents
  • Ambulatory patient

Exclusion Criteria:

  • Acute hepatic failure, biliary cirrhosis, cholestasis
  • Acute hypertension (SBP>= 180 mmHg and/or DBP >= 110 mmHg)
  • Contraindication to CPAP treatment

Sites / Locations

  • Institut Universitaire de Cardiologie et de Pneumologie de Québec (IUCPQ)Recruiting
  • Hopital Universitaire de GrenobleRecruiting
  • Clinique PasteurRecruiting
  • Hopitaux Universitaires de Genève
  • Centre Hospitalier Universitaire Vaudois

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Physical activity

Control Group

Arm Description

Obstructive sleep apnea and resistant hypertension controlled + physical activity

Obstructive sleep apnea and resistant hypertension controlled

Outcomes

Primary Outcome Measures

Systolic arterial blood pressure assessed by 24-hours home blood pressure monitoring
Systolic arterial blood pressure assessed by 24-hours home blood pressure monitoring

Secondary Outcome Measures

diastolic arterial blood pressure assessed by 24-hours home blood pressure monitoring
diastolic arterial blood pressure assessed by 24-hours home blood pressure monitoring
Mean arterial blood pressure assessed by 24-hours home blood pressure monitoring
Mean arterial blood pressure assessed by 24-hours home blood pressure monitoring
Change in physical activity: number of hour per day of physical activity
Change in physical activity: number of hour per day of physical activity
pulse wave velocity
pulse wave velocity
Change in physical activity : Metabolic Equivalents (METS)
Change in physical activity : Metabolic Equivalents (METS)
Change in physical activity : Number of steps per day
Change in physical activity : Number of steps per day
Change in sleep duration: Sleep to lying position duration ratio
Change in sleep duration: Sleep to lying position duration ratio

Full Information

First Posted
February 4, 2014
Last Updated
June 27, 2018
Sponsor
AGIR à Dom
Collaborators
University Hospital, Grenoble
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1. Study Identification

Unique Protocol Identification Number
NCT02057783
Brief Title
Physical Activity Program for Reducing Blood Pressure in Sleep Apnea Patients With Resistant Hypertension
Acronym
RAP
Official Title
Comparison of Standard Treatment by Continuous Positive Airway Pressure (CPAP) and CPAP Combined to a Physical Activity Program for Reducing Blood Pressure in Sleep Apnea Patients With Resistant Hypertension: RAP Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
June 2018
Overall Recruitment Status
Unknown status
Study Start Date
March 26, 2015 (Actual)
Primary Completion Date
July 2019 (Anticipated)
Study Completion Date
July 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
AGIR à Dom
Collaborators
University Hospital, Grenoble

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Investigators hypothesize that CPAP treatment for suppressing OSAS in combination with a physical activity program will optimize 24-hour blood pressure control in patients with OSA-related resistant hypertension.
Detailed Description
Sleep apnea syndrome, resistant hypertension and cardio-vascular risk. There are many epidemiological and clinical cohort studies demonstrating an increasing cardiovascular risk associated with Obstructive Sleep Apnea Syndrome (OSAS). In epidemiological studies, OSA severity and incident hypertension are linked in a dose-response fashion. This is true even when taking into account usual confounding factors such as age, alcohol, tobacco consumption and body mass index. More specifically, OSAS is the leading cause of refractory hypertension and OSAS prevalence is up to 80% in patients with resistant hypertension. CPAP treatment impact for reducing blood pressure in OSAS patients with resistant hypertension A recent small sample size randomized trial (n=35) demonstrated the positive impact of CPAP in decreasing both clinical and 24-hour ambulatory blood pressure. Compared to the control group, awake systolic/diastolic ambulatory blood pressure monitoring decreased significantly in the continuous positive airway pressure group (Delta: +3.1±3.3 /+2.1±2.7 vs. -6.5±3.3/ 4.5±1.9mmHg in control and CPAP groups respectively, p<0.05). Interestingly, the blood pressure changes were only observed while patients were awake, but not during nocturnal ambulatory blood pressure monitoring (Delta: +2.8±4.5/+1.8±3.5 vs. +1.6±3.5/+0.8±2.9mmHg, p=NS). HIPARCO Study, the largest Randomized Clinical Trial (RCT) in the field (n=194) recently published in JAMA (9 December 2013) also showed a significant but limited impact of CPAP on blood pressure. In an Intention To Treat analysis, CPAP significantly improved 24-h mean BP (3.0 mmHg; 95% CI 0.3 to 5.8; p=0.031) and DBP (3.2 mmHg; 95% CI 1.0 to 5.4; p=0.005) but not SBP (3.1; 95% CI -0.6 to 6.7; p=0.098). Moreover, patients in the CPAP group had 2.4 (1.2-5.1; p=0.019) times greater probability of recovering their dipper pattern. As CPAP alone is not enough in OSAS to sufficiently improve BP, further studies should address the efficacy of combined therapies in OSAS patients with resistant hypertension. Resistant hypertension and physical activity A study has recently explored the impact of a standardized exercise program in patients suffering from resistant hypertension7. In this RCT, the authors have demonstrated that the group of patients who have benefit from a physical activity program had their systolic and diastolic 24-hour ambulatory blood pressure monitoring decreasing by 6±12 and 3±7 mmHg respectively(p=0.03). Thus, the physical activity implemented in this population enabled a better control of blood pressure values. However the authors do not give any information about the presence of the absence of Sleep Apnea Syndrome (SAS) in this cohort. Study hypothesis: Investigators hypothesize that CPAP treatment for suppressing OSAS in combination with a physical activity program will optimize 24-hour blood pressure control in patients with OSA-related resistant hypertension. Originality: Up to now no study has assessed the effects of combining physical activity with CPAP treatment in patients with sleep apnea and resistant hypertension. Our work is will be the first aiming at evaluating the benefit of this combination on the control of the systolic blood arterial pressure.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypertension, Resistant to Conventional Therapy, Sleep Apnea

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Physical activity
Arm Type
Experimental
Arm Description
Obstructive sleep apnea and resistant hypertension controlled + physical activity
Arm Title
Control Group
Arm Type
No Intervention
Arm Description
Obstructive sleep apnea and resistant hypertension controlled
Intervention Type
Other
Intervention Name(s)
Physical activity
Intervention Description
Physical activity will carry out 3 times per week during 12 weeks for intervention arm
Primary Outcome Measure Information:
Title
Systolic arterial blood pressure assessed by 24-hours home blood pressure monitoring
Description
Systolic arterial blood pressure assessed by 24-hours home blood pressure monitoring
Time Frame
To baseline at 12 weeks
Secondary Outcome Measure Information:
Title
diastolic arterial blood pressure assessed by 24-hours home blood pressure monitoring
Description
diastolic arterial blood pressure assessed by 24-hours home blood pressure monitoring
Time Frame
To baseline at 12 weeks
Title
Mean arterial blood pressure assessed by 24-hours home blood pressure monitoring
Description
Mean arterial blood pressure assessed by 24-hours home blood pressure monitoring
Time Frame
To baseline at 12 weeks
Title
Change in physical activity: number of hour per day of physical activity
Description
Change in physical activity: number of hour per day of physical activity
Time Frame
To baseline at 12 weeks
Title
pulse wave velocity
Description
pulse wave velocity
Time Frame
To baseline at 12 weeks
Title
Change in physical activity : Metabolic Equivalents (METS)
Description
Change in physical activity : Metabolic Equivalents (METS)
Time Frame
To baseline at 12 weeks
Title
Change in physical activity : Number of steps per day
Description
Change in physical activity : Number of steps per day
Time Frame
To baseline at 12 weeks
Title
Change in sleep duration: Sleep to lying position duration ratio
Description
Change in sleep duration: Sleep to lying position duration ratio
Time Frame
To baseline at 12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Patient with an obstructive sleep apnea (apnea-hypopnea index > or equal to 15) Patient with resistant hypertension uncontrolled by 3 or more antihypertensive agents Ambulatory patient Exclusion Criteria: Acute hepatic failure, biliary cirrhosis, cholestasis Acute hypertension (SBP>= 180 mmHg and/or DBP >= 110 mmHg) Contraindication to CPAP treatment
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jean-Louis Pépin, Pr MD PhD
Email
JPepin@chu-grenoble.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Sandrine Bouzon
Email
sbouzon@chu-grenoble.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean-Louis Pépin, Pr MD PhD
Organizational Affiliation
Laboratoire EFCR, CHU de Grenoble, 38043, Grenoble, France
Official's Role
Principal Investigator
Facility Information:
Facility Name
Institut Universitaire de Cardiologie et de Pneumologie de Québec (IUCPQ)
City
Québec
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Simon Gakwaya
Email
Simon.Gakwaya@criucpq.ulaval.ca
First Name & Middle Initial & Last Name & Degree
Caroline Minville, MD
First Name & Middle Initial & Last Name & Degree
Frédéric Sériès, MD
First Name & Middle Initial & Last Name & Degree
Isabelle Boutin, MD
First Name & Middle Initial & Last Name & Degree
François Maltais, MD
Facility Name
Hopital Universitaire de Grenoble
City
La Tronche
ZIP/Postal Code
38700
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jean-Louis Pépin, MD PhD
Email
JPepin@chu-grenoble.fr
First Name & Middle Initial & Last Name & Degree
Sandrine Bouzon
Email
sbouzon@chu-grenoble.fr
First Name & Middle Initial & Last Name & Degree
Jean-Louis Pépin, Pr MD PhD
First Name & Middle Initial & Last Name & Degree
Renaud Tamisier, Pr MD PhD
First Name & Middle Initial & Last Name & Degree
Patrick Lévy, Pr MD PhD
First Name & Middle Initial & Last Name & Degree
Jean-Philippe Baguet, Pr MD PhD
First Name & Middle Initial & Last Name & Degree
Sandrine Launois, MD PhD
First Name & Middle Initial & Last Name & Degree
Olivier Ormezzano, MD PhD
Facility Name
Clinique Pasteur
City
Toulouse
ZIP/Postal Code
31300
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Atul Pathak, MD PhD
Phone
+33 5 62 21 21 14
Email
apathak@clinique-pasteur.com
First Name & Middle Initial & Last Name & Degree
Atul Pathak, MD PhD
First Name & Middle Initial & Last Name & Degree
Laurence Adrover, MD PhD
First Name & Middle Initial & Last Name & Degree
Nicolas Combes, MD PhD
First Name & Middle Initial & Last Name & Degree
Isabelle Billiart, MD PhD
First Name & Middle Initial & Last Name & Degree
David Attias, MD PhD
First Name & Middle Initial & Last Name & Degree
Pierre Morinet, MD PhD
Facility Name
Hopitaux Universitaires de Genève
City
Genève
Country
Switzerland
Individual Site Status
Withdrawn
Facility Name
Centre Hospitalier Universitaire Vaudois
City
Lausanne
Country
Switzerland
Individual Site Status
Withdrawn

12. IPD Sharing Statement

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Physical Activity Program for Reducing Blood Pressure in Sleep Apnea Patients With Resistant Hypertension

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