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NCT03919201 Clinical Trial

12 Weeks of Resistance Band Exercise Impacts on Adiposity, Hormones, and Blood Pressure in Postmenopausal Women

Hypertension Clinical Trial

Official title:
Impacts of 12 Weeks of Resistance Band Exercise Training on Body Composition, Aging-related Hormones, and Blood Pressure in Postmenopausal Women With Hypertension

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03919201
Other study ID # PusanNU-4
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 1, 2018
Est. completion date August 1, 2018

Study information
Verified date October 2020
Source Pusan National University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study was to examine the impacts of a 12-week resistance band exercise program on body composition, aging-related hormones, and blood pressure in postmenopausal women with stage 1 hypertension. Twenty postmenopausal women with hypertension participated in this study. Participants were randomly allocated into the resistance band training group (EX, n = 10) or the control group (CON, n = 10). The EX group performed a resistance band exercise training program at jump rope training program at 40-70% of their heart rate reserve (HRR) 5 days/week for 12 weeks (sessions 60 minutes in duration). The CON group did not participate in any exercise, dietary, or behavioral intervention. Body composition, aging-related hormones (growth hormone, insulin-like growth factor 1, dehydroepiandrosterone, and estradiol), and blood pressure were measured before and after the 12-weeks study.

Recruitment information / eligibility
Status Completed
Enrollment 20
Est. completion date August 1, 2018
Est. primary completion date July 1, 2018
Accepts healthy volunteers No
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria: - postmenopausal - hypertensive - sedentary (no regular exercise training or physical activity within previous year) Exclusion Criteria: - premenopausal - renal, pulmonary, and/or heart disease - regularly physically active

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Resistance band exercise intervention
Resistance band exercise intervention (12 weeks, 5x per week, 60 minutes per day)
• No exercise intervention group
Control group: no exercise intervention

Locations
Country Name City State
United States Song-Young Park Omaha Nebraska

Sponsors (1)
Lead Sponsor Collaborator
Pusan National University

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary estradiol Estradiol levels were measured pre- and post-exercise in picograms per milliliter (pg/mL) 12 weeks
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