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NCT05604040Completed

Home Blood Pressure Monitoring to Improve Hypertension

Home BP Monitoring with Lifestyle Changes and Mindfulness Practices to Improve Hypertension Control

Source: ClinicalTrials.gov · Last updated 25 Nov 2024

Brief summary (registry, in English)

The goal of this single group pre-post-study is to test the possibility of self-monitoring with shared medical appointments program for lifestyle education in improving blood pressure (BP) of patients with uncontrolled hypertension. The main questions it aims to address is: 1. To assess if patients with uncontrolled hypertension and their physicians will be interested in trying a program that includes self-monitoring with 6-week support for lifestyle changes and coping skills to improve BP and hypertension control. 2. To assess if patients with uncontrolled hypertension can safely participate in a program that includes self-monitoring with 6-week support for lifestyle changes and coping skills to improve their BP and ability to self-manage hypertension Participants will: * Send self-reports of their home BPs, diet, physical activity and emotions * Attend 6-week education program of lifestyle changes and coping skills delivered by physicians, holistic psychotherapists and yoga therapists.

Status (registry)
Completed
Study type
Interventional
Enrollment
33 (actual)
First submitted
9 Oct 2022
Start date
14 Oct 2022
Primary completion date
16 Jun 2023
Lead sponsor
The Cleveland Clinic
NCT number
NCT05604040

What you commit to

  • Study type: Interventional
  • Participants enrolled: 33
  • From 14 Oct 2022 to the primary completion date, 16 Jun 2023
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Have a terminal illness,
  • Severe cognitive impairment
  • Major cardiovascular or cerebrovascular event in the past 6 months (Coronary artery disease, heart valve problems, arrhythmias, heart failure, stroke)
  • Any physical or mental impairment that would affect patients' ability to participate(Ability to participate will be assessed by demonstrated ability to use available home BP machine and complete self-report during recruitment).

Other

  • On dialysis
  • Pregnant
  • Clinic BP \> systolic\>180, diastolic\>110
  • Arm circumference that exceeds the limit for the largest home BP monitor cuff

Who the study is looking for

  • Uncontrolled hypertension based on Clinic BP measurement of systolic BP\>140 or diastolic BP \>90 mm Hg (as the cutoff in the current common hypertension performance measures and ACO metrics)
  • PCP recommends or patient desires a trial of self-monitoring and lifestyle modifications
  • Patient owns a smart phone and be willing to complete self-reports of BP during study participation.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Cleveland Clinic
Coordinator of this site? Confirm its status
BeachwoodUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.