Skip to main content
Clinical Trials/NCT02694432
NCT02694432
Completed
N/A

An Internet-Assisted Mind-Body-Behavior Program for Blood Pressure Control

University of Pittsburgh1 site in 1 country76 target enrollmentSeptember 2016
ConditionsHypertension

Overview

Phase
N/A
Intervention
Not specified
Conditions
Hypertension
Sponsor
University of Pittsburgh
Enrollment
76
Locations
1
Primary Endpoint
Change in systolic blood pressure and diastolic blood pressure (mm Hg)
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

This pilot study will evaluate the feasibility of adding an online mind-body-behavior program to an existing behavioral self-management support platform that has been modified to promote achievement of blood pressure goals.

Detailed Description

Efficacious hypertension therapies are well-documented, yet 40% of treated patients do not meet the blood pressure goals set by the Joint National Committee. This gap between scientific evidence and clinical outcomes in part reflects low patient adherence to lifestyle recommendations (e.g., physical activity, weight and diet), as well as medication non-adherence. Accordingly, growing attention is focused on the need to provide patients with effective self-management support tools. In addition to finding ways to help patients adhere to currently prescribed hypertension care, it is useful to consider the range of treatment options that are offered. Evidence-based reviews have identified stress reduction as an effective tool for reducing blood pressure, yet such approaches are typically not implemented in practice. This omission represents a chance to improve the quality of hypertension care by adding stress management self-management tools. Furthermore, since patients have demonstrated a clear interest in mindfulness, the incorporation of a holistic mind-body intervention is an innovative approach to inherently patient-centered care. Increasing data supports the use of mindfulness for treating health concerns. Its holistic nature may be particularly well-suited to developing and maintaining healthy lifestyles, since lifestyle impacts diverse aspects of physical and psychological health. Yet the potential for mindfulness in health self-management has not been realized. Limited but promising data demonstrate the effectiveness of web-based counseling for behavior modification to improve common chronic disease risk factors. It is an ideal solution to provider time constraints and a potential solution to patient non-adherence to lifestyle recommendations. Health information technology provides a way to make self-management support affordable, convenient and feasible. The investigators have developed a convenient behavioral self-management support platform, "Goal-oriented Online Access to Lifestyle Support" (GOALS) for primary care patients, which has promoted weight loss and improved blood pressure control among primary care patients with weight-related cardiovascular risk factors. To maximize the ability of patients to achieve blood pressure goals, the investigators propose to add an online mind-body-behavior program to GOALS: "Minding GOALS." The investigators will evaluate the feasibility of using this program for self-management support, in coordination with primary care, in a group of 76 patients with uncontrolled hypertension. In preparation for a randomized clinical trial comparing the online tool to online traditional self-management support, the investigators will assess implementation and determine 1) the availability of eligible and willing subjects using the proposed recruitment methods, 2) the feasibility of delivering the proposed interventions in the population of interest, and 3) the viability of the proposed measurement protocols.

Registry
clinicaltrials.gov
Start Date
September 2016
End Date
March 31, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Natalia Morone

Associate Professor of Medicine & Clinical and Translational Science

University of Pittsburgh

Eligibility Criteria

Inclusion Criteria

  • Systolic blood pressure \>/= 150 mmHg and/or
  • Diastolic blood pressure \>/= 90 mmHg and
  • At least one other cardiovascular disease (CVD) risk factor (i.e., diabetes, dyslipidemia, family history of premature CVD, current smoking, obesity)

Exclusion Criteria

  • Known secondary hypertension of any etiology, malignant hypertension or hypertensive encephalopathy
  • Severe edema
  • A primary care physician (PCP) of the opinion that the patient is unable to safely undertake moderately intense unsupervised physical activity (equivalent of 30 minutes brisk walking)
  • A PCP of the opinion that the patient has inadequate cognitive function to participate
  • Previous participation in a mindfulness meditation program
  • An inability to learn adequately from English language materials
  • Current pregnancy or planned pregnancy within the next year
  • A prior diagnosis of post-traumatic stress disorder
  • Prior use of GOALS

Outcomes

Primary Outcomes

Change in systolic blood pressure and diastolic blood pressure (mm Hg)

Time Frame: Baseline, 4- and 12-months

Change in blood pressure

Secondary Outcomes

  • Change in sodium excretion (mmol/24 hr.)(Baseline and 12-months)
  • Body weight (kg)(Baseline, 4- and 12-months)
  • Body Mass Index (kg/m2)(Baseline, 4- and 12-months)
  • Physical activity (steps/day)(Baseline, 4- and 12-months)
  • Health-related quality of life(Baseline, 4- and 12-months)
  • Perceived Stress Scale(Baseline, 4- and 12-months)
  • Mindful Attention Awareness Scale(Baseline, 4- and 12-months)
  • Credibility/Expectancy Questionnaire(Baseline, 4- and 12-months)
  • PROMIS-29 Profile v2.0(Baseline, 4- and 12-months)
  • Self-reported medication adherence questions(Baseline, 4- and 12-months)

Study Sites (1)

Loading locations...

Similar Trials