Virtual Lifestyle Medicine Group Visits for High Blood Pressure
6. juli 2026 opdateret af: Puja Bharat Gandhi, The University of Texas Health Science Center, Houston
A Scalable, Lifestyle Medicine Intervention for Hypertension Using Virtual Group Shared Medical Appointments
The purpose of this study is to learn whether virtual Lifestyle medicine shared medical appointments (LMSMAs) can help people better manage their blood pressure and improve their overall health.
Studieoversigt
Status
Ikke rekrutterer endnu
Betingelser
Intervention / Behandling
Undersøgelsestype
Interventionel
Tilmelding (Anslået)
18
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiekontakt
- Navn: Puja B Gandhi, MD, MPH, DipABLM
- Telefonnummer: (713) 500-6714
- E-mail: Puja.Gandhi@uth.tmc.edu
Undersøgelse Kontakt Backup
- Navn: Natalia Williams
- Telefonnummer: (713) 486-3844
- E-mail: Natalia.Williams@uth.tmc.edu
Studiesteder
-
-
Texas
-
Houston, Texas, Forenede Stater, 77030
- The University of Texas Health Science Center at Houston
-
Kontakt:
- Puja B Gandhi, MD, MPH, DipABLM
- Telefonnummer: (713) 500-6714
- E-mail: Puja.Gandhi@uth.tmc.edu
-
Kontakt:
- Natalia Williams
- Telefonnummer: (713) 486-3844
- E-mail: Natalia.Williams@uth.tmc.edu
-
-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Ingen
Beskrivelse
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
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Lifestyle Medicine Virtual Group Visit Program plus usual medical care
|
Participants will be given a home BP monitor upon enrollment and the group will engage in twice monthly virtual shared medical appointments (vSMAs) for 4 visits.
Prior to each visit, participants will be asked to complete home BP monitoring (twice in the morning and twice in the evening for 3 days before visit), with readings reviewed during visits and medications adjusted as clinically indicated.
Participants will complete four sessions over an 8-week period, with one session type offered in each 2 week block.
Participants will be given a home BP monitor upon enrollment and will be instructed by phone and with an electronic health record (EHR) portal message on proper technique for home BP readings.
Participants will continue to have follow-up visits with their PCP as clinically indicated.
|
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Aktiv komparator: Usual medical care only
|
Participants will be given a home BP monitor upon enrollment and will be instructed by phone and with an electronic health record (EHR) portal message on proper technique for home BP readings.
Participants will continue to have follow-up visits with their PCP as clinically indicated.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Change in diastolic blood pressure readings
Tidsramme: 2-4 weeks after randomization,6 months after randomization
|
2-4 weeks after randomization,6 months after randomization
|
|
Change in systolic blood pressure readings
Tidsramme: 2-4 weeks after randomization,6 months after randomization
|
2-4 weeks after randomization,6 months after randomization
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Percentage of eligible participants who agree to participate
Tidsramme: end of study (6 months after randomization)
|
end of study (6 months after randomization)
|
|
Number of primary care physicians (PCPs) whose patients are included in the program
Tidsramme: end of study (6 months after randomization)
|
end of study (6 months after randomization)
|
|
Median number of sessions attended by each participant
Tidsramme: end of study (6 months after randomization)
|
end of study (6 months after randomization)
|
|
Adherence as assessed by the number of of blood pressure (BP) readings submitted between each session
Tidsramme: end of study (6 months after randomization)
|
end of study (6 months after randomization)
|
|
Adherence to home BP monitoring as assessed by the number of of home BP sessions submitted between each session
Tidsramme: end of study (6 months after randomization)
|
end of study (6 months after randomization)
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Efterforskere
- Ledende efterforsker: Puja B Gandhi, MD, MPH, DipABLM, The University of Texas Health Science Center, Houston
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Anslået)
3. august 2026
Primær færdiggørelse (Anslået)
3. januar 2027
Studieafslutning (Anslået)
7. februar 2027
Datoer for studieregistrering
Først indsendt
6. juli 2026
Først indsendt, der opfyldte QC-kriterier
6. juli 2026
Først opslået (Faktiske)
13. juli 2026
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
13. juli 2026
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
6. juli 2026
Sidst verificeret
1. juli 2026
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- HSC-MS-26-0577
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
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