The purpose of this study is to develop effective interventions that assist individuals with high blood pressure to quit smoking and prevent weight gain.
BACKGROUND: High blood pressure (BP), or hypertension, is a major risk factor for cardiovascular morbidity and mortality. Hypertension is associated with an elevated risk for several cardiovascular complications, including coronary heart disease, peripheral vascular disease, congestive heart failure, and stroke, as well as an increased risk for renal disease. Although there have been significant advances in the detection and treatment of high BP, approximately one in four adults in the United States is hypertensive. Cigarette smoking accounts for more than 400,000 premature deaths each year in this country alone, making it the leading cause of morbidity and mortality. Evidence from several epidemiological studies has demonstrated that, at any level of BP, smoking substantially increases the risk for all cardiovascular complications associated with hypertension. While cigarette smoking and hypertension both increase the risk of cardiovascular disease, these two risk factors act synergistically to produce a greater risk than their combined independent effects. Despite the considerable health risks, smoking among people with hypertension is very common, with a prevalence approaching that observed among those with normal BP. Unfortunately, although quitting smoking is especially important for patients with high BP, smoking cessation produces a nontrivial weight gain, averaging 5 kg, which may exacerbate hypertension in many patients with the disorder. Several studies have documented significant elevations in BP following smoking cessation, as well as increases in the prevalence of hypertension after quitting smoking. As such, it is important to develop effective interventions that assist in quitting smoking and preventing weight gain. DESIGN NARRATIVE: The objective of the trial is to recruit 750 smokers with Stage 1 hypertension or prehypertension (based on JNC VII criteria). The trial will provide all participants with a brief, validated, combined behavioral and pharmacologic smoking cessation intervention. Additionally, the study will randomly assign participants who are abstinent from smoking upon completing the cessation intervention to either a 12-week weight management and BP control program or self-help materials targeting lifestyle modification. The primary endpoint is change in BP among quit smokers at a one-year follow-up. Secondary endpoints include changes in body weight, dietary intake, urinary sodium excretion, physical activity, and relapse to smoking. Exploratory endpoints include changes in hypertensive status (e.g., movement from prehypertensive to hypertensive by JNC VII criteria) and changes in BP medication status. This is a multi-site clinical trial, with study locations in Rochester, Minnesota, and Iowa City, IA. The Rochester, MN site is currently closed for recruitment.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Enrollment
139
Nicotine replacement therapy program
Diet program
University of Iowa, Carver College of Medicine, Department of Internal Medicine, Division of General Internal Medicine
Iowa City, Iowa, United States
Mayo Clinic College of Medicine
Rochester, Minnesota, United States
Change in Systolic Blood Pressure at One Year Among People Who Have Quit Smoking
Change in systolic blood pressure in mmHg
Time frame: Measured at Year 1
Change in Diastolic Blood Pressure at One Year Among People Who Have Quit Smoking
Change in diastolic blood pressure in mmHg
Time frame: Measured at Year 1
Changes in Body Weight
Change in body weight in pounds from randomization to 12 months.
Time frame: Measured at Year 1
Dietary Intake - Fruit and Vegetable Consumption
Change in self-reported daily fruit and vegetable consumption from randomization to 12 months. Fruit and vegetable consumption was measured by self-report using a dietary screener, which provides results in the form of number of servings per day.
Time frame: Measured at Year 1
Urinary Sodium Chloride Excretion
Percent change in urinary sodium chloride (NaCL) from randomization to one-year
Time frame: Measured at Year 1
Physical Activity: Leisure Time Physical Activity in METs
Change in leisure time physical activity in metabolic equivalents (METs) from randomization to one-year. METs reflect the ratio of working metabolic rate relative to resting metabolic rate, and are expressed as the energy expended per unit of time. For this study, METs were measured based on self-reported physical activity using the International Physical Activity Questionnaire (IPAQ) and are reported in the form of MET minutes.
Time frame: Measured at Year 1
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Relapse to Smoking
Number of participants who self-reported tobacco use during the last seven-days.
Time frame: Measured at Year 1
Dietary Intake - Dietary Fat Consumption
Change in daily dietary fat consumption from randomization to 12 months.
Time frame: Measured at Year 1