Assessing Alternative Approaches for Blood Pressure Control: A3BC Trial
Hypertension

About this trial
This is an interventional treatment trial for Hypertension focused on measuring High blood pressure
Eligibility Criteria
Inclusion Criteria:
- Are at least 21 years old, and
- Have Stage 1 high blood pressure. (Defined as a systolic blood pressure between 140 mm Hg and 159 mm Hg (the top blood pressure number) and/or a diastolic blood pressure between 90 mm Hg and 99 mm Hg (the bottom blood pressure number) in the prior 6 months.)
Exclusion Criteria:
- Take drugs to control blood pressure.
- Have a history of left ventricular hypertrophy.
- Have a history of cardiovascular disease such as stroke, mini-strokes, heart attack, unstable angina, bypass surgery, stents, angioplasty, abnormal heart rhythms, heart failure, or peripheral artery disease.
- Have diabetes.
- Have a history of poor kidney function.
- Have an upper arm circumference greater than 17 inches.
- Are currently participating in a formal exercise or weight loss program.
- Plan to participate in a formal exercise or weight loss program in the next 6 months.
- Are pregnant or plan to become pregnant in the next 6 months.
Sites / Locations
- University of Michigan
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
Device Guided Breathing/Combination Therapy
Isometric Hand Grip/Combination Therapy
Participants will first do device guided breathing for 8 weeks, followed by 8 weeks of doing BOTH the device guided breathing AND the hand grip exercises. Participants will be given a home blood pressure monitor. Participants will measure blood pressure and heart rate at home for 2 weeks prior to starting any intervention and also during the 16 week of intervention.
Participants will first do isometric hand grip exercises for 8 weeks, followed by 8 weeks of doing BOTH the device guided breathing AND the hand grip exercises. Participants will be given a home blood pressure monitor. Participants will measure blood pressure and heart rate at home for 2 weeks prior to starting any intervention and also during the 16 week of intervention.