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Effects of Behavioral Stress Reduction Programs on Blood Pressure in African American Youth

Medical University of South Carolina (MUSC) logo

Medical University of South Carolina (MUSC)

Status

Completed

Conditions

Hypertension
Cardiovascular Diseases
Heart Diseases

Treatments

Behavioral: Mindfulness Meditation (MM) Program
Behavioral: Lifeskills Program (LP)
Behavioral: Health Education Control Program (CTL)

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT00241813
330
R01HL078216 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

This study will examine the effects of two behavioral stress reduction programs, mindfulness meditation (MM) and the lifeskills program (LP), and a health education control program (CTL) on blood pressure.

Full description

BACKGROUND:

African Americans (AA) experience a high prevalence and early onset of essential hypertension (EH), which has been partly attributed to exposure to chronic environmental stress. AA youth exhibit higher resting blood pressure (BP) than whites. Since BP ranking tracks from late childhood onward, AA adolescents with high normal BP are at increased risk for development of EH. The need for developing effective primary prevention programs for EH is highlighted by the fact that EH is now a pediatric problem due to recent increased prevalence among youth. There have been no previous controlled studies evaluating stress reduction approaches on BP control in AA youth, particularly within the framework of an underlying psychological and physiological-based model of stress-induced EH.

This study is in response to a 'Request for Applications' entitled "Research on Mind-Body Interactions and Health," which was issued by the Office of the Director, National Institutes of Health (NIH).

DESIGN NARRATIVE:

This study will examine the effects of two behavioral stress reduction programs, MM and LP, and CTL on cardiovascular function at rest, during laboratory stress, and in the natural environment. Participants will include 320 ninth graders (50% male) with high normal systolic BP (SBP) (SBP ranging from greater than or equal to the 50th percentile to less than or equal to the 95th percentile on three occasions). Following BP screenings and baseline evaluation, participants will be assigned to a CTL, MM, LP, or MM plus LP group. Participants will be re-evaluated after a 12-week intervention and again at a 12-week follow-up. The specific aims of this study are to determine whether MM and/or LP results in the following: 1) decreases in the primary outcome variables of resting SBP and 24-hour ambulatory SBP; 2) decreases in sympathetic nervous system (SNS) tone (decreased overnight urine norepinephrine [NE] excretion) and decreases in sodium intake (decreased overnight sodium excretion); 3) decreases in SBP reactivity to behavioral stressors; 4) decreases in SNS arousal (decreased urinary NE excretion) and greater increases in renal function (increased urinary sodium excretion) to the behavioral stressors; 5) decreases in self-reported hostility and anger; 6) improvement in vascular function (increases in percent of endothelium-dependent arterial vasodilation to reactive hyperemia); and 7) improvement in ventricular structure and function (decreases in left ventricular mass index and resting heart rate). It is anticipated that the combination of MM and LP will result in greater positive impacts than either treatment alone. The study will be conducted by teachers during school health classes. If these programs are shown to be successful, they may be incorporated into the regular school curriculum.

Enrollment

283 patients

Sex

All

Ages

14 to 17 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • In ninth grade
  • SBP ranging from greater than or equal to 50th percentile to less than or equal to 95th percentile on three occasions

Exclusion criteria

  • Clinical Hypertension

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

283 participants in 4 patient groups

Health Education Control Program (CTL)
Active Comparator group
Description:
Health Education Control Program (CTL)
Treatment:
Behavioral: Health Education Control Program (CTL)
Mindfulness Meditation
Experimental group
Description:
Mindfulness Meditation (MM) Program
Treatment:
Behavioral: Mindfulness Meditation (MM) Program
Lifeskills
Experimental group
Description:
Lifeskills Program (LP)
Treatment:
Behavioral: Lifeskills Program (LP)
MM plus LP
Experimental group
Description:
Mindfulness Meditation (MM) Program plus Lifeskills Program (LP)
Treatment:
Behavioral: Lifeskills Program (LP)
Behavioral: Mindfulness Meditation (MM) Program

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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