Handgrip Training and Brain Blood Flow Regulation

NCT ID: NCT07223645

Last Updated: 2025-11-20

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-10-27

Study Completion Date

2028-10-27

Brief Summary

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This study aims to investigate the effect of isometric handgrip training on brain blood vessel function in physically inactive adults. Isometric handgrip training is a promising strategy for lowering blood pressure and improving vascular health, but no previous investigations have studied the effect of training on markers of brain blood vessel function. Based on previous work showing improvements in vascular function after isometric handgrip training, we hypothesize that isometric handgrip training will improve key markers of cerebrovascular function.

Detailed Description

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The incidence of cerebrovascular diseases is expected to increase. Early life sets the stage for vascular health outcomes later in life. Regular exercise is recommended for improving cerebrovascular health outcomes, but a lack of time or inadequate facilities are common exercise barriers. Not getting enough exercise is associated with worse cardiovascular and cerebrovascular health outcomes. There is a critical need for time-efficient strategies that require minimal equipment for improving cardiovascular and cerebrovascular health. Isometric handgrip (IHG) training is an effective strategy for improving cardiovascular health. Despite IHG's usefulness for improving vascular health through blood pressure reductions and improvements in endothelial function, almost nothing is known about IHG training and cerebrovascular function. Therefore, this project aims to test the hypothesis that 8 weeks of IHG training will improve cerebrovascular blood flow regulation and total cerebrovascular blood flow among adult humans who are not meeting the physical activity recommendations. We will measure middle cerebral artery blood velocity (MCAv) via transcranial Doppler ultrasound and assess MCAv dynamic autoregulation and MCAv reactivity to high and low carbon dioxide. We will also measure total cerebral blood flow, central artery stiffness, and MCAv pulsatility index. Understanding the effect of IHG on cerebrovascular health could inform exercise recommendations.

Conditions

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Inactivity/Low Levels of Exercise

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

TRIPLE

Participants Investigators Outcome Assessors

Study Groups

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Isometric Handgrip Training - Intervention

Participants will perform moderate-intensity handgrip training three days per week for eight weeks using a handheld device.

Group Type EXPERIMENTAL

Handgrip Training

Intervention Type DEVICE

Handgrip training 3 days per week for 8 weeks

Isometric Handgrip Training - Sham

Participants will perform very low-intensity handgrip training three days per week for eight weeks using a handheld device.

Group Type SHAM_COMPARATOR

Handgrip Training

Intervention Type DEVICE

Handgrip training 3 days per week for 8 weeks

Interventions

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Handgrip Training

Handgrip training 3 days per week for 8 weeks

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* 18 to 35 years old
* Body mass index ≤30 kg/m2 (without obesity)
* Physically inactive (not meeting the current recommendations of ≥150 minutes per week of moderate-to-vigorous aerobic exercise and not ≥2 days per week of resistance training) in last 6 months
* Have a smartphone and are willing to download mobile applications used in this project

Exclusion Criteria

* Having an overt chronic condition (e.g., cardiovascular, cerebrovascular, etc.)
* Being pregnant, planning to become pregnant, or breastfeeding/lactating
* Regular use of nicotine products in the past 6 months
* Recent head injury/trauma or concussion
Minimum Eligible Age

18 Years

Maximum Eligible Age

35 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Florida State University

OTHER

Sponsor Role lead

Responsible Party

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Joseph Watso

Laboratory Director

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Florida State University

Tallahassee, Florida, United States

Site Status RECRUITING

Countries

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United States

Facility Contacts

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Joseph Watso, PhD

Role: primary

850-644-5260

Other Identifiers

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STUDY00006271

Identifier Type: -

Identifier Source: org_study_id

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