- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03615625
Post-exercise Hypotension After a Power Training Session in Older Adults With Hypertension
Effect of a Power Training Session on Ambulatory Blood Pressure in Older Adults With Hypertension: a Randomized Crossover Trial
The main purpose of the present study was to evaluate the effect of a power training session on office and 24h ambulatory blood pressure in older adults with hypertension. As secondary outcomes, the investigators compared post-exercise hypotension, BP variability, and endothelial function between older men and women with hypertension.
The working hypothesis was that a single bout of power exercise would decrease both office and 24 h BP in comparison to a non-exercising control session and men and women would respond differently after a power training session.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
RS
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Porto Alegre, RS, Brazil, 90035-903
- Hospital de Clínicas de Porto Alegre
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Office blood pressure between 130-179 and 80-110 mmHg for systolic and diastolic blood pressure, respectively;
- Non-engaged in structured programs of exercise for the last 3 months since the beginning of this study;
- Able to perform the proposed exercises.
Exclusion Criteria:
- Underlying cardiovascular disease previously diagnosticated by a doctor, occurred in the last 24 months, such as: acute myocardial infarction, angina, stroke or heart failure;
- Diseases that reduce life expectancy;
- Smokers and ex-smokers for less than six months;
- BMI > 39.9 kg/m²
- diabetic proliferative retinopathy.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: CROSSOVER
- Masking: TRIPLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
NO_INTERVENTION: Control session
Control session without any exercise.
The participants remained in seated rest throughout 40 min
|
|
|
EXPERIMENTAL: Power Training Session
The power training session lasted 40 min, in which the participants performed a resistance exercise session using high velocity contractions during the exercises characterizing a power training session
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3 sets of 8-10 repetitions of 5 exercises performed in the following order: leg press, bench press, knee extension, upright row, and knee flexion, using an intensity corresponding to 50 % of 1-RM and two-minute intervals between sets and exercises.
The concentric phase of exercises during each repetition was performed "as fast as possible" while the eccentric phase lasted 1-2 seconds.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Ambulatory Blood Pressure Monitoring
Time Frame: 24 hours after control and power training exercise session
|
Mean 24-h, day-time, night-time of blood pressure in mmHg will be assessed after each experimental session (power training session and control session)
|
24 hours after control and power training exercise session
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Office Systolic Blood Pressure
Time Frame: 60 minutes after control and power training exercise session
|
Systolic blood pressure in mmHg will be measured using automatic oscillometric before and after each experimental session throughout one hour
|
60 minutes after control and power training exercise session
|
|
Office Diastolic Blood Pressure
Time Frame: 60 minutes after control and power training exercise session
|
Diastolic blood pressure in mmHg will be measured using automatic oscillometric before and after each experimental session throughout one hour
|
60 minutes after control and power training exercise session
|
|
Endothelial Function
Time Frame: 60 minutes after control and power training exercise session
|
Flow-mediated dilatation (FMD) assessed through high resolution ultrasonography before and after each experimental session throughout one hour
|
60 minutes after control and power training exercise session
|
|
Blood Pressure Variability
Time Frame: 24 hours after control and power training exercise session
|
Systolic and diastolic BP values obtained in the 24-hour ambulatory blood pressure monitoring, with valid measures included in a programmed software to calculate the average real variability of these measures.
|
24 hours after control and power training exercise session
|
Other Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Sex Differences in Ambulatory Blood Pressure Monitoring, Office Blood Pressure, Endothelial Function and Blood Pressure Variability
Time Frame: 60 minutes and 24 hours after control and power training exercise session
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60 minutes and 24 hours after control and power training exercise session
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Collaborators and Investigators
Collaborators
Publications and helpful links
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 85210618.1.0000.5327
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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