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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03544307
Other study ID # TaekwondoMenopause
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 1, 2017
Est. completion date March 1, 2018

Study information

Verified date November 2020
Source Kosin University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Aging is associated with hormonal imbalances and progressive decreases in arterial health and function. It is crucial to prevent or reduce the negative effects of aging on hormonal balance and the vasculature by implementing appropriate lifestyle interventions, such as exercise training. We examined the effects of a 12-week Taekwondo training program on blood catecholamines, arterial stiffness (pulse wave velocity, PWV), blood pressure (BP), resting heart rate, and muscular strength in postmenopausal women with stage 2 hypertension.


Description:

Using a parallel experimental design, participants were randomly assigned to either a Taekwondo exercise training group (n=10) or non-exercising control group (n=10) for 12 weeks. Participant in the Taekwondo training group trained 3 days/week for 60 minutes per session, and the intensity progressed weekly. Participants in the control group performed no exercise intervention.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date March 1, 2018
Est. primary completion date March 1, 2018
Accepts healthy volunteers No
Gender Female
Age group 65 Years to 85 Years
Eligibility Inclusion Criteria: - Be diagnosed with stage-2 hypertension - Be postmenopausal - Be between 65 and 85 years old Exclusion Criteria: - Known cardiovascular, metabolic or renal diseases - Physical limitations that prohibit exercise - Participates in regular exercise

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Taekwondo training
Exercise group

Locations

Country Name City State
United States University of Nebraska Omaha Omaha Nebraska

Sponsors (2)

Lead Sponsor Collaborator
Kosin University University of Nebraska

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Blood Epinephrine Levels 12-weeks
Primary Blood Norepinephrine Levels 12-weeks
Secondary Arterial Stiffness Pulse Wave Velocity 12-weeks
Secondary Systolic Blood Pressure 12-weeks
Secondary Hand Grip Strength 12-weeks
Secondary Diastolic Blood Pressure 12-weeks
Secondary Leg Strength 12-weeks
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