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Can mindfulness lower blood pressure? new study investigates

NCT ID NCT07679984

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 This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jul 01, 2026 · Last updated Jul 07, 2026 · Updated 3 times

Summary

This study tests whether adding an 8-week online mindfulness program, called Mindfulness in Motion, to usual care helps people with high blood pressure improve their blood pressure, weight, stress, sleep, and well-being. Participants will be randomly assigned to either the mindfulness program plus usual care or usual care alone. Over 12 months, they will complete short questionnaires about stress, sleep, and resilience.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Mindfulness in Motion (MIM) program
What this could lead to
If it works, this could offer a simple, drug-free way to help manage high blood pressure and reduce stress.
What could go wrong
This is a small, early-stage study with 140 participants, so results may not apply to everyone. The mindfulness program may not lower blood pressure significantly.

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

About 140 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Oct 2026

An estimate. Start dates often move.

Expected to finish

May 2028

An estimate. End dates often move.

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

18 years and older

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: 1. Age \>18 years old. 2. Established patient at OSU Family Medicine 3. Diagnosis of primary essential hypertension 4. Ability and willingness to participate in all Mindfulness in Motion (MIM) study activities. 5. Ability and willingness to download MyCap, the smartphone app that securely links participant study responses to the REDCap study project. 6. WiFi connectivity or LTE to allow use of MIM smartphone app and MyCap when not at OSU clinical site. Exclusion Criteria: 1. Inability to read and/or understand English (MIM intervention, study consent and questionnaires in English). 2. Established mindfulness practice. 3. Diagnosis of secondary hypertension with identifiable underlying causes including: * Chronic kidney disease * Renal artery stenosis * Primary aldosteronism * Cushing's syndrome * Pheochromocytoma * Obstructive sleep apnea * Medication induced hypertension (e.g., steroids, NSAIDs) * Pregnancy related hypertension 4. Current severe alcohol or substance abuse disorder. 5. Participants with documented cognitive disorder that limits the ability to independently participate in MIM program, read, understand, and/or complete the surveys; i.e. dementia, Alzheimer's or biological tests. 6. Participants with major psychiatric disorders not controlled by medication or other psychiatric treatments.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • The Ohio State University Wexner Medical Center

    Columbus, Ohio, 43210, United States

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