Impact of Resistance Training Intensity on Blood Pressure

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age50-70
SponsorUniversité de Sherbrooke

About this trial

The goal of the clinical trial is to understand the effect of two resistance training protocols employing different loading intensities (% of 1 repetition maximum; 1-RM), but with standardized effort intensity (2 repetitions in reserve; RIR) on post-exercise and ambulatory blood pressure in aging females.

The main questions it aims to answer are:

* to examine the acute effects of low (50% 1-RM) and high (80% 1-RM) load intensity resistance exercise with a standardized high effort intensity on post-exercise hypotension and ambulatory blood pressure responses in aging females; * deepen the understanding of the mechanisms underlying acute reductions in blood pressure in response to resistance exercise performed at different load intensities. To this end, autonomic activity will be estimated alongside the measurement of central arterial compliance (i.e., carotid artery), and serum biomarkers of endothelial function; * document the affective valence and enjoyment associated with low (50% 1-RM) and high (80% 1-RM) load intensity resistance exercise when performed at a high perceived effort.

Researchers will compare the effect of: 1) a low load (LL-RE) intensity protocol consisting of 3 sets of each exercise at 50% 1-RM, performed until reaching a hard perceived effort intensity (i.e., RIR-2); 2) high load (HL-RE) intensity protocol consisting of 3 sets of each exercise at 80% of 1-RM, performed until reaching a hard perceived effort intensity (i.e., RIR-2); 3) and a control condition (CON) consisting of a standardized non-fatiguing cognitive task.

Participants will participate in:

* A preliminary assessment visit; * Two familiarization visits to validate the exercise prescriptions; * Three experimental visits (CON, LL-RE, HL-RE).

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

aged 50 to 70 years;

absence of menstruation for 12 consecutive months;

normal-high resting blood pressure (120 ≤ Systolic ≤ 139 mmHg and 80 ≤ Diastolic ≤ 89 mmHg) or stage 1 hypertension (140 ≤ Systolic ≤ 159 mmHg or 90 < Diastolic ≤ 99 mmHg);

physically inactive (< 150 minutes of structured aerobic physical activity per week);

Disqualifiers

orthopedic limitations or other contraindications to resistance exercise;

scheduled surgery during the study;

unstable hypertension (≥ 160/100 mmHg);

diagnosis of type 2 diabetes;

Trial design

Design model

Crossover

Treatments tested in this trial

  • Condition LL-RE

    Other intervention

    LL-RE condition will consist of a 5-minute warm-up (slow-paced walking) and the following exercises: leg press, chest press, leg curl, and seated row. Three sets will be performed for each exercise with a 3-minute rest period between sets/exercises. Each exercise will be executed through a full range of motion, with participants encouraged to follow a 2-sec eccentric phase (guided by a mobile app metronome and supervised by an exercise physiologist) and to perform the concentric phase as fast as possible. Participants will be informed to: stop the set when they perceive to have reached the RIR target. • LL-RE: The low load intensity protocol consists of 3 sets of each exercise at 50% 1-RM, performed until reaching a hard perceived effort intensity (i.e., RIR-2).

  • Control

    Other intervention

    Control condition: During the control condition, participants will sit quietly in a room maintained at a temperature of 22-24°C to prevent any influence on blood pressure values, for 60 minutes. During this period, they will perform a standardized non-fatiguing cognitive task: watching Earth, a documentary following the migration paths of four animal families.

  • Condition HL-RE

    Other intervention

    HL-RE condition will consist of a 5-minute warm-up (slow-paced walking) and the following exercises: leg press, chest press, leg curl, and seated row. Three sets will be performed for each exercise with a 3-minute rest period between sets/exercises. Each exercise will be executed through a full range of motion, with participants encouraged to follow a 2-sec eccentric phase (guided by a mobile app metronome and supervised by an exercise physiologist) and to perform the concentric phase as fast as possible. Participants will be informed to: stop the set when they perceive to have reached the RIR target. • HL-RE: The high load intensity protocol consists of 3 sets of each exercise at 80% of 1-RM, performed until reaching a hard perceived effort intensity (i.e., RIR-2).

Treatment groups

36 Participants
are divided into 3 treatment groups
Group A: Condition LL-REExperimental treatment 1 intervention
Group B: Condition HL-REExperimental treatment 1 intervention
Group C: Condition CONSham comparator 1 intervention

Trial outcomes

Primary outcomes

1

Change in blood pressure post-exercise

Oscillometric blood pressure monitor

Time frame
Before the start of the condition (t = 0 minute), at the end of the condition (t = 60 minutes), each 20 min for 1 hour post-condition (t = 80, 100, 120 minutes)
2

Change in ambulatory blood pressure

Ambulatory blood pressure monitor

Time frame
During 24 hours after the condition

Secondary outcomes

1

Heart rate variability

Heart rate monitor

Time frame
Before the start of the condition (t = 0 minute), at the end of the condition (t = 60 minutes), each 20 min for 1 hour post-condition (t = 80, 100, 120 minutes), during 24 hours after the condition
2

Carotid artery diameter as assessed by Cardiovascular Suite v4.6.1

Doppler ultrasound

Time frame
Before the start of the condition (t = 0 minute), at the end of the condition (t = 60 minutes), 1 hour post-condition (t = 120 minutes)
3

Carotid artery distensibility as assessed by Cardiovascular Suite v4.6.1

Doppler ultrasound

Time frame
Before the start of the condition (t = 0 minute), at the end of the condition (t = 60 minutes), 1 hour post-condition (t = 120 minutes)
4

Carotid artery blood flow velocity

Doppler ultrasound

Time frame
Before the start of the condition (t = 0 minute), at the end of the condition (t = 60 minutes), 1 hour post-condition (t = 120 minutes)

Other outcomes

1

Velocity loss in concentric contraction speed

Video camera

Time frame
Continuously during the condition (t = 0 minute to t = 60 minutes)
2

Hematocrit/hemoglobin concentration

Hemoglobin analyzer

Time frame
At the end of the condition (t = 60 minutes)
3

Estimated daily energy expenditure

Accelerometer

Time frame
During 24 hours after the condition
4

Time spent in the different sedentary behaviors

Accelerometer

Time frame
During 24 hours after the condition

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