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Blood PressureNCT06215014

Sex Effects on Blood Pressure With Handgrip Training

A study testing Isometric handgrip training in people with Blood Pressure, run by University of Massachusetts, Boston at 2 sites in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The goal of this intervention is to compare the blood pressure response of young females and males to a single bout of static handgrip exercise before and after static handgrip training (4 weeks). Read more about this study

Who is it for?
Ages 18 to 40 yearsHealthy volunteers can take part
Conditions the study is for
Blood Pressure
What is being tested?
Isometric handgrip training
Could I receive a placebo?
No, everyone receives an active treatment
How many people
29 participants
Where
2 sitesUnited States
Study dates
1 Mar 2024to 18 Jun 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 40 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Ages between 18-40 years;
  • Normal blood pressure as defined by the American Heart Association (<130/90 mmHg);
  • BMI < 30 kg/m2;
  • No cardiovascular risk factors and no clinically diagnosed cardiovascular disease;
  • Being recreationally active (≤ 2 days of structured physical activity);
  • Able to speak English.

Who cannot join

  • Diagnosed with cardiovascular disease (e.g., coronary artery disease, heart failure), musculoskeletal (i.e., osteoporosis and sarcopenia), metabolic disease (e.g., diabetes mellitus) and kidney disease;
  • Taking antihypertensive or other vasoactive medications and cardioactive medication;
  • Diagnosed with depression and/or anxiety disorders;
  • Long COVID;
  • Being a smoker;
  • Being pregnant or having menstrual irregularities.

Trial locations and contacts

2 sites in 1 country.

United States2 sites
  • UMassachusetts Boston

    Boston, Massachusetts, 02125

  • University of Massachusetts Boston

    Boston, Massachusetts, 02125

Other trials in United States

About this study

Official title: Sex Effects on Blood Pressure Regulation to Acute Isometric Handgrip Exercise, Following 4 Weeks of Isometric Handgrip Training

The goal of this intervention is to compare the blood pressure response of young females and males to a single bout of static handgrip exercise before and after static handgrip training (4 weeks).

The main questions this study aims to answer are:

Read more
  • Are the lowering blood pressure effects of static handgrip exercise training different between young females and males?
  • Which factors explain the lowering blood pressure effects of static handgrip training and possible differences between sexes? Is it an improved blood vessel dilation? Is it a reduced stiffening of blood vessels? Is it a reduced fight or flight response resulting in a lower heart rate and blood pumped by the heart into the vessels? All the above?
  • Which factors regulate blood pressure response during and immediately after a single bout of static handgrip exercise?

All participants will be asked to:

  • Visit the laboratory to perform static handgrip exercise - first visit;
  • Participants will be randomized (like flipping a coin) to static handgrip exercise training or to a non-exercising phase, with each phase lasting four weeks. Participants will also complete the other condition (handgrip or no handgrip) after completing the first four-week condition
  • Return to the laboratory after the completion of both static handgrip training and no training to perform the static handgrip exercise of the first visit.

The investigators will compare participants' blood pressure response to a single bout static of handgrip exercise after training to their own blood pressure response to the same bout of exercise after the non-training period.

Read the detailed description

Hypertension is still the leading modifiable risk factor for cardiovascular disease and a silent independent predictor of all-cause death worldwide. Projections for the US suggest that 41% of adults will develop hypertension before 2030. Thus, it is clinically relevant to optimize interventions aimed at preventing and managing hypertension.

Isometric handgrip training holds promise to mitigate the growing prevalence of hypertension in healthy adults. This form of exercise training can be performed at home, requires less time investment compared to conventional training, and requires only one piece of inexpensive equipment. Interestingly, some but not all studies suggest that isometric handgrip training yields superior antihypertensive effects in young healthy males compared to their female counterparts. The mechanisms behind the antihypertensive effects of isometric handgrip training are yet to be determined. Possible candidates include: 1) increases in cardiovagal modulation and 2) increases in endothelial nitric oxide-dependent vasodilation coupled with reductions in arterial stiffness.

The understanding of blood pressure (BP) regulation to acute isometric handgrip exercise would provide valuable mechanistic insight into possible sex-dependent antihypertensive effects of this form of training, given that acute responses likely translate into antihypertensive training adaptations. In fact, in healthy young adults, an acute bout of isometric handgrip exercise has been shown to evoke a higher blood pressure response in males compared to females immediately after exercise cessation. Given that higher hypertensive responses to acute isometric handgrip exercise are associated with greater reductions in resting BP following isometric handgrip training, this could explain the larger antihypertensive effects reported in young males. Importantly, young females are generally less fatigable to isometric handgrip exercise performed at the same relative intensity than males. This sex difference in muscle fatigability relates to the larger muscle mass and strength of males leading to higher intramuscular pressures that compress feeding arteries but also to the smaller increments in blood pressure of females to exercise. Importantly, whether this sex difference in fatigability and blood pressure during acute isometric handgrip exercise limits the potential for blood pressure-related adaptations to handgrip training in females is unknown. In addition, young females also exhibit a faster BP recovery to acute isometric handgrip exercise than their male counterparts. Mechanistically, this faster recovery is, in part, attributed to faster cardiovagal reactivation and higher increases in baroreflex sensitivity observed in females but not in males. However, whether other regulatory mechanisms, such as increases in endothelial nitric oxide-mediated vasodilation and or reductions in sympathetic outflow to blood vessels contribute to this apparently faster blood pressure recovery in females after a hypertensive stimulus is unknown. In addition, blood flow and baroreflex dynamics interplay during isometric handgrip exercise are largely unknown which might provide valuable insight into blood pressure regulation after exercise cessation.

Therefore, the specific aims of this study are threefold:

Aim 1 - To examine if the effects of a 4-week isometric handgrip training intervention on BP regulation to a fatiguing bout of isometric handgrip exercise are sex- dependent in young healthy adults with normal BP

Aim 2 - To examine if blood pressure responses are sex-dependent during and after a fatiguing bout of isometric handgrip exercise at 30% maximum voluntary contraction in healthy young adults with normal blood pressure;

Aim 3 - To determine the effects of sex on the regulatory mechanisms of blood pressure, including cardiac autonomic and vascular function during and after a fatiguing bout of isometric handgrip exercise in healthy young adults with normal BP.

Conditions
Blood Pressure
Being tested
Isometric handgrip training
Keywords
exercise training, handgrip, sex effects

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Isometric handgrip trainingOther

    Participants will train three days per week at home for 1 month using a reliable and validated digital handgrip dynamometer (DynX, MD System, Inc., Westerville, USA) in a seated position. The isometric handgrip training protocol will consist of four sets (2 for each hand) of two-min sustained contractions starting at 30% of maximum voluntary contraction (MVC) interspersed by 1-min resting periods (a total of 12-min). All training sessions will be remotely supervised via Zoom or phone call by a research team member to ensure compliance with the exercise prescription. Before each training session, MVCs will be re-assessed over three repetitions, each separated by 30-s, to ensure an accurate exercise prescription. The highest value will be used to determine the target intensity of the session

Study groups in NCT06215014
Study groupRoleWhat they receive
Handgrip trainingExperimentalParticipants will perform isometric handgrip training 3 days per week for a month.
Receives: Other: Isometric handgrip training
ControlNo interventionParticipants will not perform isometric handgrip training for a month.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Brachial blood pressure

    Systolic and diastolic blood pressure

    Measured: "Baseline, pre-intervention/oscillometry", "Within 5-days after the intervention/oscillometry"

  2. Flow-mediated dilation

    Non-invasive measurement of endothelial function

    Measured: "Baseline, pre-intervention/ultrasonography", "Within 5-days after the intervention/ultrasonography"

  3. Root mean square of successive differences (RMSSD)

    Heart rate variability metric of the time domain reflecting cardiovagal modulation

    Measured: "Baseline, pre-intervention/electrocardiography", "Within 5-days after the intervention/electrocardiography"

  4. High frequency power band

    Heart rate variability metric of the spectral domain reflecting cardiovagal modulation

    Measured: "Baseline, pre-intervention/electrocardiography", "Within 5-days after the intervention/electrocardiography"

  5. Carotid femoral pulse wave velocity (cfPWV)

    Central arterial stiffness

    Measured: "Baseline, pre-intervention/ultrasonography", "Within 5-days after the intervention/applanation tonometry"

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Jan 2024
  2. Study start1 Mar 2024
  3. Primary completion18 Jun 2025
  4. Study completion18 Jun 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Crossover
Masking
None (open label)
Enrolment
29 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06215014
Sponsor's protocol ID
3471
Status last verified
May 2026
First submitted
27 Sep 2023
Last updated
12 May 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Isometric handgrip training in people with Blood Pressure, run by University of Massachusetts, Boston at 2 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 12 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Brachial blood pressure (time frame: "Baseline, pre-intervention/oscillometry", "Within 5-days after the intervention/oscillometry"). The study lists 5 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 May 2026.

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