Tension Tamer Randomized Control Trial
Primary Purpose
Pre-hypertension
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Tension Tamer (TT)
Lifestyle education program (SPCTL)
Sponsored by
About this trial
This is an interventional prevention trial for Pre-hypertension focused on measuring Breathing Awareness Meditation,
Eligibility Criteria
Inclusion Criteria:
- 18-90 years old, male or female, African American (AA) or White;
- Stage 1 or 2 pre-hypertensive (i.e., SBP 120-139/DBP<90) based upon 2 consecutive clinic evaluations;
- Body Mass Index (BMI) 18.5 -45 Kg/m2;
- legally competent;
- able to use a smart phone.
Exclusion Criteria:
- failure to meet any inclusion criteria;
- type two diabetes or chronic kidney disease (GFR<50 mL/1.7 m2/min.);
- cancer diagnosis or treatment in past 2 years;
- prior cardiovascular event, congestive heart failure or angina;
- prior or current psychiatric illness;
- ongoing substance abuse (e.g., >21 drinks/week);
- pharmacologic medications which may influence blood pressure (BP);
- planned pregnancy;
- vulnerable populations such as pregnant or nursing women, prisoners, and institutionalized individuals.
Sites / Locations
- Medical University of South Carolina
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Tension Tamer (TT)
Lifestyle education program (SPCTL)
Arm Description
Breathing Awareness Mediation delivered by smartphone app.
Healthy lifestyle education provided by text messages and links to media. Runkeeper app to log physical activity.
Outcomes
Primary Outcome Measures
Resting BP
Resting SBP reduction target -7 mmHg.
Secondary Outcome Measures
Ambulatory SBP
24-hr SBP reduction target -4 mmHg.
Full Information
NCT ID
NCT03168789
First Posted
May 25, 2017
Last Updated
January 13, 2020
Sponsor
Medical University of South Carolina
1. Study Identification
Unique Protocol Identification Number
NCT03168789
Brief Title
Tension Tamer Randomized Control Trial
Official Title
Smartphone Delivered Meditation for BP Control Among Prehypertensives
Study Type
Interventional
2. Study Status
Record Verification Date
January 2020
Overall Recruitment Status
Completed
Study Start Date
October 1, 2016 (Actual)
Primary Completion Date
November 22, 2019 (Actual)
Study Completion Date
November 22, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Medical University of South Carolina
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
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.
Detailed Description
80 stage 1 or 2 pre-hypertensive adults, will be randomly assigned to 2x daily TT at scheduled decreasing doses or enhanced standard of care lifestyle education program delivered via smartphone (SPCTL) for 12 months. Subjects will participate in 5 study visits at baseline/enrollment, 1, 3, 6 , and 12 months
TT subjects will be given the TT app. The app provides instructions on breathing awareness meditation (BAM): focusing upon the moment by sustaining one's attention upon diaphragm movements and related sensations while breathing in a slow, deep, relaxed manner. One learns to passively observe thoughts, images and extraneous sounds without making judgments about them. BAM doesn't involve analysis of historical or recent stressful experiences, but instead centers upon learning to stay in the present moment while meditating. The app will also collect heart rate (HR) values during each session using the phone's camera. The duration of the TT sessions will begin at 15 min., decrease to 10 min., and finally decrease to 5 min. Adherence will be monitored by the receipt of date-stamped heart rate values collected during each meditation session.
SPCTL subjects will be provided Runkeeper app and taught how to record physical activity they perform. Recommended dosage of using SPCTL media and/or app will be that of the TT group. Adherence to SPCTL will be assessed using server file analyses of modules used and activity recorded in Runkeeper.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pre-hypertension
Keywords
Breathing Awareness Meditation,
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
80 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Tension Tamer (TT)
Arm Type
Experimental
Arm Description
Breathing Awareness Mediation delivered by smartphone app.
Arm Title
Lifestyle education program (SPCTL)
Arm Type
Active Comparator
Arm Description
Healthy lifestyle education provided by text messages and links to media. Runkeeper app to log physical activity.
Intervention Type
Behavioral
Intervention Name(s)
Tension Tamer (TT)
Intervention Description
Tension Tamer is an app that provides training and motivation for breathing awareness meditation (BAM). The app also tracks heart rate values during each session by placing a finger tip over the rear camera.
Intervention Type
Behavioral
Intervention Name(s)
Lifestyle education program (SPCTL)
Intervention Description
SPCTL group will use Runkeeper app to log physical activity. They will also receive text messages with short healthy lifestyle tips, and links to media with pamphlets or videos with more in-depth information.
Primary Outcome Measure Information:
Title
Resting BP
Description
Resting SBP reduction target -7 mmHg.
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Ambulatory SBP
Description
24-hr SBP reduction target -4 mmHg.
Time Frame
12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
18-90 years old, male or female, African American (AA) or White;
Stage 1 or 2 pre-hypertensive (i.e., SBP 120-139/DBP<90) based upon 2 consecutive clinic evaluations;
Body Mass Index (BMI) 18.5 -45 Kg/m2;
legally competent;
able to use a smart phone.
Exclusion Criteria:
failure to meet any inclusion criteria;
type two diabetes or chronic kidney disease (GFR<50 mL/1.7 m2/min.);
cancer diagnosis or treatment in past 2 years;
prior cardiovascular event, congestive heart failure or angina;
prior or current psychiatric illness;
ongoing substance abuse (e.g., >21 drinks/week);
pharmacologic medications which may influence blood pressure (BP);
planned pregnancy;
vulnerable populations such as pregnant or nursing women, prisoners, and institutionalized individuals.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Frank A Treiber, PhD
Organizational Affiliation
MUSC College of Nursing
Official's Role
Principal Investigator
Facility Information:
Facility Name
Medical University of South Carolina
City
Charleston
State/Province
South Carolina
ZIP/Postal Code
29425
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
30010353
Citation
Adams ZW, Sieverdes JC, Brunner-Jackson B, Mueller M, Chandler J, Diaz V, Patel S, Sox LR, Wilder S, Treiber FA. Meditation smartphone application effects on prehypertensive adults' blood pressure: Dose-response feasibility trial. Health Psychol. 2018 Sep;37(9):850-860. doi: 10.1037/hea0000584. Epub 2018 Jul 16.
Results Reference
derived
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Tension Tamer Randomized Control Trial
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