Could virtual lifestyle groups tame high blood pressure?
NCT ID NCT07698509
First seen Jul 13, 2026 · Last updated Jul 14, 2026 · Updated 1 time
Summary
This study explores whether virtual group medical appointments focused on lifestyle changes can help people with high blood pressure lower their readings. Participants attend four online sessions over eight weeks, track their blood pressure at home, and get medication adjustments as needed. The goal is to see if this approach is practical and effective for managing hypertension.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- lifestyle medicine virtual group shared medical appointments
- What this could lead to
- If successful, this approach could offer a scalable, convenient way for people with high blood pressure to better manage their condition through lifestyle changes and remote monitoring.
- What could go wrong
- This is a small, early-stage study with only 18 participants, so results may not apply to everyone. The intervention relies on participant engagement, which may vary.
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
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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
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About 18 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2026
An estimate. Start dates often move.
- Expected to finish
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Feb 2027
An estimate. End dates often move.
- Lead sponsor
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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
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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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 Hide 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: * Current diagnosis of hypertension (ICD codes I10.0-I14.0 billed within the last 5 years Essential HTN, Essential HTN, Primary HTN) * Currently receives care at a UTPhysicians; Last seen by a PCP at Victory location within the last 1 year. * Able to participate in a virtual format * Willingness to participate and engage in home blood pressure monitoring Exclusion Criteria: * Unstable cardiovascular disease (recent Myocardial Infarction (MI), unstable angina, decompensated HF) * Advanced Chronic kidney disease (CKD) (eGFR \< 30) without nephrology co-management * Active cancer treatment * Severe cognitive impairment (unable to engage) * Uncontrolled psychiatric illness (e.g., active psychosis) * Resistant hypertension (requiring\> 3 medications at maximum doses) * Unable to participate in English class format * Unstable internet or lack of smartphone
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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.
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The places running it
1 site. The list below names each one and where it is.
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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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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
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The University of Texas Health Science Center at Houston
Houston, Texas, 77030, United States
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