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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04044638
Other study ID # 2.821.574
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 5, 2018
Est. completion date April 30, 2018

Study information

Verified date August 2019
Source Universidade Regional do Cariri
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Introduction: Strength training (ST) is an important non-pharmacological means to reduce blood pressure (BP). Objective: To verify the pressure response of women after 8 weeks of ST. Method: Fourteen women were divided into young group (YG) and middle age (MAG) and submitted to ST for 8 weeks, lasting 60 minutes in 11 alternating exercises per segment with intensity of 12 to 13 on the subjective perception scale of effort. BP was verified at weeks 1, 4 and 8.


Description:

The sample consisted of 14 women, which were divided into two groups: young group (YG = 7) and middle age group (MAG = 7). Inclusion criteria were: females aged 18 to 59 years, sedentary or who had not been engaged in any physical activity in the last 6 months, and the availability of time three times a week in the afternoon shift. Exclusion criteria were: morbid obesity (BMI> 40 kg.m-2), presenting any osteo-articular dysfunction.

After the adaptation period, resistance exercise sessions were started, which were performed 3 times a week on alternate days, in which each session lasted 60 minutes, and performed for a period of 8 weeks. Each session consisted of 10-minute warm-up on the treadmill or bicycle, shortly after, starting the exercises in the form of alternating circuit by segment, as: machine bench press, extension chair, high pull (front), flexor table, direct curl, leg press, triceps pulley, adductor, abdominal, abductor and calf. In all 10 exercises, 3 sets of 8 to 12 repetitions were performed, with an interval of 60 seconds between sets and intensity of 12 arbitrary units (a.u.) to 14 a.u., measured by the rate perception effort scale. In the first, fourth and eighth week, pre-exercise blood pressure (BP) was verified, in which the participants sat for a period of 10 minutes at rest, in a comfortable chair, with legs uncrossed, feet flat on the floor, back leaning on the chair, left arm at heart level and palm up1 to measure BP using a G * Tech-branded automatic digital device (MASTER MA100 model).


Recruitment information / eligibility

Status Completed
Enrollment 14
Est. completion date April 30, 2018
Est. primary completion date April 2, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 59 Years
Eligibility Inclusion Criteria:

- Females between 18 and 59 years old, sedentary or who had not been engaged in any physical activity in the last 6 months, plus the availability of time three times a week in the afternoon shift.

Exclusion Criteria:

- Morbid obesity (BMI> 40 kg.m-2), presenting any osteo-articular dysfunction that limited the performance of exercises in strength training, women who were classified in category 3 (known serious disease) after risk stratification of the College American of Sports Medicine and also, who presented cardiovascular diseases, autonomic neuropathy, diabetes and hypertension controlled or not.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Resistance trainining
Resistance training sessions were held 3 times a week, in which each session lasted 60 minutes and was performed for a period of 8 weeks. Each session consisted of 10-minute warm-up, shortly after, starting the exercises in the form of alternating circuit by segment, as: machine bench press, extension chair, high pull (front), flexor table, direct curl, leg press, triceps pulley, adductor, abdominal, abductor and calf. In all 10 exercises, 3 sets of 8 to 12 repetitions were performed, with an interval of 60 seconds between sets and intensity of 12 arbitrary units (a.u.) to 14 a.u., measured by the rate perception effort scale. In the first, fourth and eighth week, pre-exercise blood pressure (BP) was verified, in which the participants sat for a period of 10 minutes at rest, in a comfortable chair, with legs uncrossed, feet flat on the floor, back leaning on the chair, left arm at heart level and palm up to measure BP using a G * Tech-branded automatic digital device (MASTER model).

Locations

Country Name City State
Brazil Alfredo Anderson Teixeira de Araujo Juazeiro Do Norte CE

Sponsors (1)

Lead Sponsor Collaborator
Universidade Regional do Cariri

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary Blood pressure Increased blood pressure in young group and reduced blood pressure in middle age group Four weeks
Primary Blood pressure Increased blood pressure in young group and reduced blood pressure in middle age group Eight weeks
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