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New exercise combo shows promise for lowering blood pressure

NCT ID NCT07470450

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jul 29, 2026 · Updated 2 times

Summary

This study looked at whether combining two types of strength training (dynamic and isometric) can lower blood pressure more than doing just one type. Researchers studied 60 middle-aged adults with high blood pressure who were already on medication. Participants did different exercise sessions, and their blood pressure was monitored for 24 hours. The goal was to see if the combined approach offers extra benefits for managing hypertension.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

60 people

The number who actually took part.

Started

Jul 2025

Finished

Dec 2025

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

30 to 60 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: Clinical diagnosis of stage 1 or stage 2 hypertension, according to current guidelines. Sedentary lifestyle (no participation in structured exercise training for at least 6 months). Age between 18 and 60 years. Stable antihypertensive pharmacological treatment for at least 4 weeks before enrollment. Ability to perform resistance exercise. Exclusion Criteria: Symptomatic cardiovascular disease. Heart failure. Unstable angina. Uncontrolled diabetes mellitus (HbA1c \> 8%). Renal insufficiency. Musculoskeletal disorders or physical limitations that contraindicate resistance exercise. Changes in antihypertensive medication within the 4 weeks prior to enrollment or during the study protocol. Current smoking. Excessive alcohol consumption.

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Conditions

The condition(s) this trial relates to.

hypertensive disorder Post-Exercise Hypotension

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Universidade Federal do Rio Grande do Sul

    Porto Alegre, Rio Grande do Sul, 91420-550, Brazil

More trials for these conditions

Other studies related to the condition(s) this trial covers.