- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05310006
Acute Effects of Low and High-Speed Resistance Training on Blood Pressure in Older Adults: A Crossover Study
Study Overview
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
SP
-
Poá, SP, Brazil, 08562-460
- Lar Mãe Mariana Nursing Home
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Aged ≥60 years; Frail according to Fried's criteria (Fried et al., 2009); Possessed sufficient physical and cognitive abilities to perform all exercises required by the protocol; Had a physician authorization to participate of exercise programs.
Exclusion Criteria:
Participation in a structured physical exercise training program in the past six months; Prescription of hormone replacement therapy and/or psychotropic drugs; Presence of any acute cardiovascular event (e.g., myocardial infarction) or complication in the past six months.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: High Speed Resistance Exercise (HSRE)
Exercise sessions performed using eight times (sets) with 4-5 repetitions at 70-75% of the maximal strength.
The concentric phase was performed as fast as possible, and the eccentric phase was carried out for 2 s.
|
Exercise sessions were performed in the morning (07:00 am-12:00 am) under the supervision of at least two fitness instructors in the rehabilitation unit of the nursing home.HSRE and TRE were designed according to the peculiarities of each type of resistance exercise (Chodzko-Zajko et al., 2009).
During TRE, participants performed four sets of 8-10 repetitions at 70-75% of the maximal strength.
The concentric and eccentric phases were carried out for 2 s.
For HSRE, exercises were performed eight times (sets) with 4-5 repetitions at 70-75% of the maximal strength.
The concentric phase was performed as fast as possible, and the eccentric phase was carried out for 2 s.
Bilateral calf raise was performed using the same load as unilateral knee extension.
|
Experimental: Traditional Resistance Exercise (TRE)
Exercise sessions were performed using four sets of 8-10 repetitions at 70-75% of the maximal strength.
The concentric and eccentric phases were carried out for 2 s.
|
Exercise sessions were performed in the morning (07:00 am-12:00 am) under the supervision of at least two fitness instructors in the rehabilitation unit of the nursing home.HSRE and TRE were designed according to the peculiarities of each type of resistance exercise (Chodzko-Zajko et al., 2009).
During TRE, participants performed four sets of 8-10 repetitions at 70-75% of the maximal strength.
The concentric and eccentric phases were carried out for 2 s.
For HSRE, exercises were performed eight times (sets) with 4-5 repetitions at 70-75% of the maximal strength.
The concentric phase was performed as fast as possible, and the eccentric phase was carried out for 2 s.
Bilateral calf raise was performed using the same load as unilateral knee extension.
|
No Intervention: Control Session (CS)
Participants remained seated in a comfortable chair listening to music and/or talking with study investigators for approximately 30 min.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Blood Pressure
Time Frame: Immediately after the end of the experimental sessions
|
Blood Pressure
|
Immediately after the end of the experimental sessions
|
Blood Pressure
Time Frame: 10 minutes after the end of the experimental sessions
|
Blood Pressure
|
10 minutes after the end of the experimental sessions
|
Blood Pressure
Time Frame: 20 minutes after the end of the experimental sessions
|
Blood Pressure
|
20 minutes after the end of the experimental sessions
|
Blood Pressure
Time Frame: 30 minutes after the end of the experimental sessions
|
Blood Pressure
|
30 minutes after the end of the experimental sessions
|
Blood Pressure
Time Frame: 50 minutes after the end of the experimental sessions
|
Blood Pressure
|
50 minutes after the end of the experimental sessions
|
Blood Pressure
Time Frame: 60 minutes after the end of the experimental sessions
|
Blood Pressure
|
60 minutes after the end of the experimental sessions
|
Blood Pressure
Time Frame: 24 hours after the end of the experimental sessions
|
Blood Pressure
|
24 hours after the end of the experimental sessions
|
Collaborators and Investigators
Sponsor
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
- 20021919
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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