Pre-hypertension Clinical Trial
Official title:
Smartphone Delivered Meditation for BP Control Among Prehypertensives
Verified date | January 2020 |
Source | Medical University of South Carolina |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study is 12 months long and consists of 5 visits at baseline, months 1, 3, 6, and 12. To determine eligibility potential subjects will have resting blood pressures (BP) measured on 2 occasions. Pre-hypertensive individuals will be invited to participate in the study. After informed consent is obtained, subjects will complete baseline visit consisting of a survey, resting BP, wear activity watch for 7 days ambulatory blood pressure monitor for 24-hours, collect saliva and urine samples. Subjects will then be randomly assigned to Tension Tamer (TT) or lifestyle education program delivered via smartphone (SPCTL) groups. At the remaining 4 visits subjects will again complete a survey, resting BP, wear activity watch for 7 days ambulatory blood pressure monitor for 24-hours, collect saliva and urine samples. Throughout the 12 months TT group will meditate twice daily and SPCTL group will log physical activity.
Status | Completed |
Enrollment | 80 |
Est. completion date | November 22, 2019 |
Est. primary completion date | November 22, 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 90 Years |
Eligibility |
Inclusion Criteria: 1. 18-90 years old, male or female, African American (AA) or White; 2. Stage 1 or 2 pre-hypertensive (i.e., SBP 120-139/DBP<90) based upon 2 consecutive clinic evaluations; 3. Body Mass Index (BMI) 18.5 -45 Kg/m2; 4. legally competent; 5. able to use a smart phone. Exclusion Criteria: 1. failure to meet any inclusion criteria; 2. type two diabetes or chronic kidney disease (GFR<50 mL/1.7 m2/min.); 3. cancer diagnosis or treatment in past 2 years; 4. prior cardiovascular event, congestive heart failure or angina; 5. prior or current psychiatric illness; 6. ongoing substance abuse (e.g., >21 drinks/week); 7. pharmacologic medications which may influence blood pressure (BP); 8. planned pregnancy; 9. vulnerable populations such as pregnant or nursing women, prisoners, and institutionalized individuals. |
Country | Name | City | State |
---|---|---|---|
United States | Medical University of South Carolina | Charleston | South Carolina |
Lead Sponsor | Collaborator |
---|---|
Medical University of South Carolina |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Resting BP | Resting SBP reduction target -7 mmHg. | 12 months | |
Secondary | Ambulatory SBP | 24-hr SBP reduction target -4 mmHg. | 12 months |
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