Mechanisms of the Relaxation Response in Elderly Hypertensives

Sponsor
National Center for Complementary and Integrative Health (NCCIH) (NIH)
Overall Status
Completed
CT.gov ID
NCT00913991
Collaborator
(none)
69
1
2
33
2.1

Study Details

Study Description

Brief Summary

Systolic Hypertension is a disorder which is characterized by significant elevations in systolic blood pressure in association with normal diastolic blood pressure. Typically, this develops in individuals >50 years of age and is associated with an increased risk of stroke and myocardial infarction. While there are many effective therapies for essential/diastolic hypertension, the treatment of systolic hypertension is complicated by side effects from traditional therapies. This limits therapeutic options and has resulted in a number of at-risk individuals being left untreated.

We are conducting a randomized, controlled trial (n=90) to compare the effects of two different stress management training on blood pressure. The primary outcome is change in systolic blood pressure and pulse pressure. Secondary outcomes are changes in nitric oxide, stress hormones and psychological well-being. Additional analyses will be conducted to assess for other confounding effects on BP and PP.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Stress Management Training
  • Behavioral: Stress Management Training
Phase 1

Study Design

Study Type:
Interventional
Actual Enrollment :
69 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Basic Science
Official Title:
Mechanisms of the Relaxation Response in Elderly Hypertensives
Study Start Date :
Mar 1, 2009
Actual Primary Completion Date :
Jun 1, 2011
Actual Study Completion Date :
Dec 1, 2011

Arms and Interventions

Arm Intervention/Treatment
Experimental: Stress Management #1

8 weeks of individual stress management training sessions

Behavioral: Stress Management Training
Weekly 60-minute session with a trainer for 8 consecutive weeks. Daily home practice of approximately 20 minutes per day via CD.

Active Comparator: Stress Management #2

8 weeks of individual stress management training sessions

Behavioral: Stress Management Training
Weekly 60-minute session with a trainer for 8 consecutive weeks. Daily home practice of approximately 20 minutes per day via CD.

Outcome Measures

Primary Outcome Measures

  1. Systolic Blood Pressure [8 weeks]

Secondary Outcome Measures

  1. Nitric Oxide and epinephrine levels [8 weeks]

Eligibility Criteria

Criteria

Ages Eligible for Study:
55 Years to 100 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Male or female; stage I SH (140-159 mm Hg SBP and < 90 mm Hg DBP), > 55 years of age; taking at least 1 anti-hypertensive medication at a stable dose for 1 month preceding the screening visit; understanding of English; normal hearing; and able to provide informed consent.
Exclusion Criteria:
  • Presence of current neurological, psychiatric, medical or musculoskeletal disorder; current asthma; severe seasonal allergies resulting in screening NO values > 60 ppb; current smoking; experience with yoga, meditation, guided imagery or other techniques that evoke the RR; hematocrit below 32; glucose lower than 50 or higher than 200; a creatinine greater than 1.3, Mini-Mental Status Exam score less than 26 or clinical depression based on a score of greater than 15 on the CES-D and Health Counselor's clinical evaluation. Subjects can not take the following medications: beta-agonist bronchodilators, systemic corticosteroids, anti-convulsants, immunosuppressive or cytotoxic therapy (currently or within the last 12 months), anabolic steroids, anti-depressants (not including SSRIs), anti-psychotics, chronic sypathomimetic medications, and dicyclomine.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Abbott Northwestern Hospital Minneapolis Minnesota United States 55410

Sponsors and Collaborators

  • National Center for Complementary and Integrative Health (NCCIH)

Investigators

  • Principal Investigator: Jeffery Dusek, PhD, Allina Health System

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Dusek, Jeffery, Research Director, National Center for Complementary and Integrative Health (NCCIH)
ClinicalTrials.gov Identifier:
NCT00913991
Other Study ID Numbers:
  • R21AT003315-01
First Posted:
Jun 4, 2009
Last Update Posted:
Sep 11, 2019
Last Verified:
Feb 1, 2010
Keywords provided by Dusek, Jeffery, Research Director, National Center for Complementary and Integrative Health (NCCIH)
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 11, 2019