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Hair salons join the fight against high blood pressure in women of color

NCT ID NCT07042386

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Sep 09, 2026 · Updated 4 times

Summary

This pilot study will test whether training hair stylists to check blood pressure, combined with home monitoring, health coaching, and pharmacist support, can help Black and Hispanic women lower their blood pressure. About 144 women who visit participating salons will be randomly assigned to the full program or enhanced usual care. The study focuses on feasibility and early signs of effectiveness.

What this could mean

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

Active substance
behavioural intervention (salon-based blood pressure screening, home monitoring, coaching, pharmacist support)
What this could lead to
If successful, this could provide a practical, community-based way to help Black and Hispanic women manage high blood pressure and reduce related health risks.
What could go wrong
This is a small pilot study (144 participants) testing feasibility, not a large trial. It may not show significant blood pressure improvement or be scalable to other communities.

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 144 people

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

Started

May 2026

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 to 79 years

Sex

Female participants only

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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: Women are eligible if: * At least 18 years old * Self-identify as Black/African American or Hispanic * Have an average seated systolic blood pressure of 130 mmHg or higher on initial salon screening, and * Have visited the participating salons at least twice in the past six months. Exclusion Criteria: Women are excluded if: * Pregnant or planning pregnancy during the study period * Have end-stage renal disease requiring dialysis * Have serious medical conditions limiting life expectancy to less than 12 months * Currently participating in other cardiovascular intervention studies * Have severe cognitive impairment, impeding informed consent * Unable to operate blood pressure monitoring equipment after training * Plan to relocate outside the study area within 6 months * Have documented adverse reactions to blood pressure cuff usage.

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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.

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  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

  • Johns Hopkins University

    RECRUITING

    Baltimore, Maryland, 21205, United States

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