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Hypertension (HTN)NCT07453550

The Effects of Brief Periods of Exercise on Blood Pressure

A study testing wall-squat and wall-squat-tradition in people with Hypertension (HTN) and Pre Hypertension, run by University of Hartford at 1 site in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

High blood pressure is a common medical condition that affects the body's arteries. It's also called hypertension. Untreated hypertension increases the risk of heart attack, stroke and other serious health problems. Exercise is a promising tool in hypertension management. Read more about this study

Who is it for?
Ages 18 to 55 yearsHealthy volunteers can take part
Conditions the study is for
Hypertension (HTN), Pre Hypertension
What is being tested?
wall-squat and wall-squat-tradition
Could I receive a placebo?
No, everyone receives an active treatment
How many people
45 participants
Where
1 siteUnited States
Study dates
1 Feb 2026to Jun 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

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 55 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • 18-55 yrs.
  • 24 hour average BP >110/70 mmHg, but < 160 systolic blood pressure
  • Able to provide informed consent

Who cannot join

  • Currently taking anti-hypertensive medication smokers and alcohol drinkers Inability to undertake exercise intervention (resistance and isometric exercise)
  • Current medical history of any of the following:
  • hyperaldosteronism Diabetes mellitus (Type 1 or type 2) Heart disease Stroke or transient ischemic attack Peripheral neuropathy Aortic aneurysm and/or peripheral arterial disease If female, pregnancy or currently breast feeding Enrolled in another Clinical Trial of an Interventional Medicinal Product or Medical Device or other interventional study Medical condition that, in the opinion of the investigator, would make the participant unsuitable for the study On long term warfarin Allergies to blood pressure cuff materials or ultrasound gel
  • Previous medication history of any of the following:
  • hyperaldosteronism Heart disease Stroke or transient ischemic attack Peripheral neuropathy Aortic aneurysm and/or peripheral arterial disease thromboembolism Infection within limb within 3 months On long term warfarin Allergies to blood pressure cuff materials or ultrasound gel

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Jinghui Yang, PT, MPT, PhD contact

347-429-0843

jiyang@hartford.edu

United States1 site, 1 recruiting
  • University of Hartford

    West Hartford, Connecticut, 06117

    Jinghui Yang, 3474290843, jiyang@hartford.edu

    Recruiting

Other trials in United States

About this study

High blood pressure is a common medical condition that affects the body's arteries. It's also called hypertension. Untreated hypertension increases the risk of heart attack, stroke and other serious health problems. Exercise is a promising tool in hypertension management. Regular participation in exercise improves vascular health, heart and lung function, and multisystem health. However, the direct evidence of the treatment effects of a brief period of exercise on blood pressure in individuals with hypertension is limited. A brief period of exercise refers to an exercise protocol that only lasts for a very short period of time, such as 5-10 minutes.

Read the detailed description

The study will investigate both acute and long-term effects of a brief exercise on blood pressure. For the acute effect, participants will conduct a single bout of resistance exercise (leg press) with or without blood flow restriction technique. The blood pressure changes from pre- to post-exercise will be monitored. The long-term effect of exercise on blood pressure will be examined through a six to eight weeks home-based intervention program. Participants will conduct two forms of exercise, one is a clustered wall-sit exercise and the other is a scattered wall-sit exercise.

Being tested
wall-squat, wall-squat-tradition
Keywords
isometric exericse
Medical subject headings
Hypertension, Prehypertension

What participants receive

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

  • wall-squatBehavioural

    the experimental group will complete the four sets of wall-squats at four different times across the day: morning, noon, afternoon, night.

  • wall-squat-traditionBehavioural

    The other exercise group will do 4 sets of wall squat in a continuous way.

Study groups in NCT07453550
Study groupRoleWhat they receive
Non-Ex control groupNo interventionNot described
Clustered Ex ConditionActive comparatorNot described
Receives: Behavioral: wall-squat-tradition
Scattered Ex ConditionExperimentalNot described
Receives: Behavioral: wall-squat

What is being measured

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

  1. 24 h blood pressure

    The average, peak and variations of 24 h SBP and DBP, daytime SBP and DBP, night time SBP and DBP will be measured before and after the intervention.

    Measured: From the enrollment to the end of the study at six weeks

Secondary outcomes (2)
  1. endothelial function

    endothelial function measured by flow mediated dilation

    Measured: at baseline (Day 1) and Week 6

  2. arterial stiffness

    arterial stiffness measured by pulse wave velocity

    Measured: at baseline (Day 1) and week 6

Timeline

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

  1. First posted6 Mar 2026
  2. Study start1 Feb 2026
  3. Primary completionDec 2026 (estimated)
  4. Study completionJun 2027 (estimated)

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
Parallel groups
Model description
For the acute study, a cross-over design will be used to allow each participant to go through both conditions. For the long-term study, a randomized controlled study design will be used.
Masking
Double blind
Who is masked
Investigator, Outcomes assessor
Enrolment
45 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07453550
Sponsor's protocol ID
25-12-505
Status last verified
Feb 2026
First submitted
15 Feb 2026
Last updated
1 May 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: The data and protocol can be shared with other researchers by request after publication.

Questions about this trial

What is this clinical trial studying?

A study testing wall-squat and wall-squat-tradition in people with Hypertension (HTN) and Pre Hypertension, run by University of Hartford at 1 site 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 3 inclusion and 5 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: looking for participants now, as of the sponsor's last update on 1 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 1 site 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?

This study is still under way. Results are not available in the source record yet.

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

Contact Jinghui Yang, PT, MPT, PhD (347-429-0843, jiyang@hartford.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

24 h blood pressure (time frame: From the enrollment to the end of the study at six weeks). 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 1 May 2026.

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