Purpose

The treatment of high blood pressure, or hypertension, is multifaceted and can include pharmacological therapies (i.e., medications) and lifestyle modifications such as physical activity. Chronotherapy, which describes timing of a treatment with the body's daily rhythms, has recently been used with hypertension medications and has been shown to be effective at lowering blood pressure and reducing the risk of cardiovascular disease events. Specifically, taking medications in the evening was shown to be more effective than morning medication routines. Little information is available about the effectiveness of chronotherapy combined with exercise (i.e., planned physical activity) interventions in older adults with hypertension. The purpose of this study is to examine how exercise training performed in the morning and early evening affects blood pressure and other measures of blood vessel health in postmenopausal females with hypertension.

Condition

Eligibility

Eligible Ages
Between 55 Years and 80 Years
Eligible Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Systolic BP equal to or greater than 130 mmHg without BP medication or greater than 120 mmHg with medication and diastolic blood pressure equal to and greater than 80 mmHg - 55-80 years old - Post-menopausal female - Able to walk without assistance

Exclusion Criteria

  • Habitually physically active defined as 150 minutes of moderate-intensity or 75 minutes of vigorous-intensity aerobic physical activity per week - Overt pulmonary disease/condition as follows: chronic bronchitis, chronic obstructive pulmonary disease, emphysema, or pulmonary hypertension - Cardiometabolic disease/condition as follows: diabetes, heart failure, peripheral arterial disease, stroke, coronary artery disease, renal disease, secondary hypertension, chronic venous insufficiency or deep vein thrombosis within last 6 months - Cancer within last 5 years - Body mass index >39 kg/m2 - Current smoking or vape - Evening shift work - uncontrolled thyroid disorder - 2 or more falls in the last year - Anemia within 3 months of enrollment - Parkinson's disease - Dementia - Unstable angina - Acute pulmonary embolus or infarction - Acute myocarditis or pericarditis - Acute aortic dissection

Study Design

Phase
N/A
Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover Assignment
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Morning (AM)
Exercise starting before 10:01 AM
  • Behavioral: 6 weeks of exercise training (Pre-training)
    handgrip and treadmill walking 4 days per week
  • Behavioral: 6 weeks of exercise training (Post-training)
    handgrip and treadmill walking 4 days per week
Experimental
Evening (PM)
Exercise starting after 3:59 PM
  • Behavioral: 6 weeks of exercise training (Pre-training)
    handgrip and treadmill walking 4 days per week
  • Behavioral: 6 weeks of exercise training (Post-training)
    handgrip and treadmill walking 4 days per week

Recruiting Locations

Michigan State University
East Lansing 4991640, Michigan 5001836 48824
Contact:
Jill Slade, PhD
517-884-3351
jslade@msu.edu

More Details

Status
Recruiting
Sponsor
Michigan State University

Study Contact

Jill Slade, PhD
5178843351
jslade@msu.edu

Detailed Description

Blood pressure has an internal rhythm associated with the 24-hr clock. Nocturnal blood pressure (BP) is a key contributor to cardiovascular health and may be improved by exercise. Moreover, the time of day of the exercise may be a key factor. This study aims to evaluate the effects of morning and evening exercise training on BP and other measures of vascular function in older females with hypertension.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.