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Preventing Weight Gain and Controlling Blood Pressure During Smoking Cessation in Hypertensive Smokers

Primary Purpose

Cardiovascular Diseases, Heart Diseases, Hypertension

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Nicotine Replacement Therapy
Diet
Sponsored by
University of Iowa
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Cardiovascular Diseases

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Smoke at least 5 cigarettes/day (or have quit within the last 6 weeks to enter the study for the weight gain prevention and BP control interventions) Pre-hypertensive or Stage I hypertension (systolic BP from 120 to 159 and/or diastolic BP from 80 to 99 mm Hg). Antihypertensive medications are not criteria for exclusion provided that BP is not over 160/100 mm Hg) Access to a telephone Exclusion Criteria: History of unstable cardiovascular disease, including myocardial infarction, stroke, and unstable angina within three months of study start Coronary artery bypass grafting or angioplasty/stent within three months of study start Cardiac dysrhythmia treated with anti-arrhythmia medication, except stable atrial fibrillation Untreated hyperthyroidism or pheochromocytoma History of congestive heart failure (NYHA Class III or IV) ECG evidence of 2nd or 3rd degree atrioventricular block Uncontrolled or Stage II Hypertension as defined as BP consistently above 160/100 mm Hg History of severe liver or kidney failure Current substance abuse (includes alcohol use in excess of 21 drinks a week) Presence of an unstable psychiatric condition Severe chronic obstructive pulmonary disease Symptomatic peripheral vascular disease Pulmonary hypertension with shortness of breath Congenital or valvular heart disease with shortness of breath Current use of a medication that may interfere with primary study endpoints or that may increase the risk of side effects from study medication that cannot be discontinued Pregnant or plans to become pregnant within the next year Planning to move out of the area or travel extensively during the intervention Any medical condition that would preclude any additional changes in diet Unable to further modify physical activity routine Cannot engage in moderate intensity exercise (e.g., walking)

Sites / Locations

  • University of Iowa, Carver College of Medicine, Department of Internal Medicine, Division of General Internal Medicine
  • Mayo Clinic College of Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

1

2

Arm Description

Weight management and BP control program

Self-help materials targeting lifestyle modification

Outcomes

Primary Outcome Measures

Change in BP among people who have quit smoking

Secondary Outcome Measures

Changes in body weight
Dietary intake
Urinary sodium excretion
Physical activity
Relapse to smoking

Full Information

First Posted
June 3, 2005
Last Updated
January 7, 2013
Sponsor
University of Iowa
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)
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1. Study Identification

Unique Protocol Identification Number
NCT00113074
Brief Title
Preventing Weight Gain and Controlling Blood Pressure During Smoking Cessation in Hypertensive Smokers
Official Title
Blood Pressure Control in Hypertensive Smokers
Study Type
Interventional

2. Study Status

Record Verification Date
January 2013
Overall Recruitment Status
Completed
Study Start Date
September 2004 (undefined)
Primary Completion Date
June 2011 (Actual)
Study Completion Date
June 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Iowa
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to develop effective interventions that assist individuals with high blood pressure to quit smoking and prevent weight gain.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiovascular Diseases, Heart Diseases, Hypertension

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
376 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Description
Weight management and BP control program
Arm Title
2
Arm Type
Active Comparator
Arm Description
Self-help materials targeting lifestyle modification
Intervention Type
Drug
Intervention Name(s)
Nicotine Replacement Therapy
Intervention Description
Nicotine replacement therapy program
Intervention Type
Behavioral
Intervention Name(s)
Diet
Intervention Description
Diet program
Primary Outcome Measure Information:
Title
Change in BP among people who have quit smoking
Time Frame
Measured at Year 1
Secondary Outcome Measure Information:
Title
Changes in body weight
Time Frame
Measured at Year 1
Title
Dietary intake
Time Frame
Measured at Year 1
Title
Urinary sodium excretion
Time Frame
Measured at Year 1
Title
Physical activity
Time Frame
Measured at Year 1
Title
Relapse to smoking
Time Frame
Measured at Year 1

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Smoke at least 5 cigarettes/day (or have quit within the last 6 weeks to enter the study for the weight gain prevention and BP control interventions) Pre-hypertensive or Stage I hypertension (systolic BP from 120 to 159 and/or diastolic BP from 80 to 99 mm Hg). Antihypertensive medications are not criteria for exclusion provided that BP is not over 160/100 mm Hg) Access to a telephone Exclusion Criteria: History of unstable cardiovascular disease, including myocardial infarction, stroke, and unstable angina within three months of study start Coronary artery bypass grafting or angioplasty/stent within three months of study start Cardiac dysrhythmia treated with anti-arrhythmia medication, except stable atrial fibrillation Untreated hyperthyroidism or pheochromocytoma History of congestive heart failure (NYHA Class III or IV) ECG evidence of 2nd or 3rd degree atrioventricular block Uncontrolled or Stage II Hypertension as defined as BP consistently above 160/100 mm Hg History of severe liver or kidney failure Current substance abuse (includes alcohol use in excess of 21 drinks a week) Presence of an unstable psychiatric condition Severe chronic obstructive pulmonary disease Symptomatic peripheral vascular disease Pulmonary hypertension with shortness of breath Congenital or valvular heart disease with shortness of breath Current use of a medication that may interfere with primary study endpoints or that may increase the risk of side effects from study medication that cannot be discontinued Pregnant or plans to become pregnant within the next year Planning to move out of the area or travel extensively during the intervention Any medical condition that would preclude any additional changes in diet Unable to further modify physical activity routine Cannot engage in moderate intensity exercise (e.g., walking)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mark W. Vander Weg, PhD
Organizational Affiliation
University of Iowa, Carver College of Medicine, Department of Internal Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Iowa, Carver College of Medicine, Department of Internal Medicine, Division of General Internal Medicine
City
Iowa City
State/Province
Iowa
Country
United States
Facility Name
Mayo Clinic College of Medicine
City
Rochester
State/Province
Minnesota
ZIP/Postal Code
55905
Country
United States

12. IPD Sharing Statement

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Preventing Weight Gain and Controlling Blood Pressure During Smoking Cessation in Hypertensive Smokers

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