RecruitingNot Applicable

Impact of Resistance Training Intensity on Blood Pressure

Canada36 participantsStarted 2025-07-08

Plain-language summary

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).

Who can participate

Age range50 Years – 70 Years

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * 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); * and not engaging in regular resistance exercise (≥ 2 sessions per week) for more than 3 months during the year. Exclusion Criteria: * orthopedic limitations or other contraindications to resistance exercise; * scheduled surgery during the study; * unstable hypertension (≥ 160/100 mmHg); * diagnosis of type 2 diabetes; * cardiovascular event in the past 6 months or sequelae preventing exercise; * and initiation of hormonal replacement therapy (\< 4 months) known to affect blood pressure.

What they're measuring

Change in blood pressure post-exercise

Timeframe: 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)

Change in ambulatory blood pressure

Timeframe: During 24 hours after the condition

Trial details

NCT IDNCT06845514

SponsorUniversité de Sherbrooke

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2028-05

Contact for this trial

Eléonor Riesco, Ph.D.

819-821-8000 e.riesco@usherbrooke.ca