Effect of Plyometric Exercises in Premenopausal Women

March 18, 2021 updated by: Kübra Alpay, Bezmialem Vakif University

The Effect of Plyometric Exercises on Muscle Strength in Premenopausal Women

It was aimed to examine the effects of plyometric exercises on muscle strength in this study. 26 premenopausal women assigned to one of the three groups: Control Group (n=8), Plyometric Exercise Group (n=10) and Isokinetic Exercise Group (n=8). Muscle strength assessments, depression and anxiety inventories were performed baseline and after 6 weeks.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Depending on various factors, bone mass begins to decrease with aging and this may lead to the osteoporosis. Physical activity and regular exercise provides an increase in bone mineral density (BMD). It is mentioned that there are relationships between muscle strength and BMD and also muscle strength has positive effects on BMD. In the literature it is showed that postmenopausal women with weaker trunk muscle strength could have risk of osteoporosis.

Plyometric exercises are used to increase muscle strength. Physiological basis of plyometric exercise consist of stretch-shortening cycle and thus it is effective in increasing the force. At the same time, plyometric exercises have positive effects on BMD because of weight bearing exercises.

The aim of this study was to investigate the effects of plyometric exercises on hip and trunk muscle strength in premenopausal women.

Participants and Study Design: Twenty six sedentary premenopausal women aged 35-50 years participated this study. Participants were assigned into three groups: Plyometric Exercise Group (PG; n=10), Isokinetic Exercise Group (IG; n=8), Control Group (CG; n=8). Participants were informed about the procedures of the study and signed a written voluntary consent form in accordance with the Declaration of Helsinki. The study protocol was approved by the Ethical Committee of the Istanbul University Medical Faculty. Measurements and training sessions were performed in the Istanbul University Medical Faculty Sport Medicine Department's Laboratory.

Measurements: Muscle strength was determined by using a Cybex Norm isokinetic dynamometer (Cybex Humac Norm, USA). Range of motion was set from 10 degree extension to 40 degree flexion. Isokinetic concentric contraction strength was measured at angular velocity of 60 degree per second and 90 degree per second. Subjects performed 3 trials trunk flexion and extension contractions at minimal exertion and 4 test repetitions at maximal trunk flexion and extension.

The hip abduction adduction isokinetic testing was performed in side lying position. Hip muscle strength was measured at angular velocity of 30 degree per second. Range of motion was set from 10 degree adduction to 40 degree abduction. Subjects performed 4 trials at minimal exertion and 4 test repetitions. Dominant leg values were analyzed for hip. All subjects performed warm-up and stretching exercises before testing.

Beck Depression Inventory (BDI) and State-Trait Anxiety Inventory (STAI) were used to asses depression and anxiety conditions.

Interventions: The training sessions were performed three days a week for six weeks. All exercise sessions were supervised by a physiotherapist.

Each session was consisted of warm-up, plyometric exercises and cool-down periods in PG. The warm-up and cool-down periods were performed by walking on the treadmill and lower extremity stretching exercises. The plyometric exercise training period involved vertical jumping, forward and back jumping and lateral jumping. After fifth session the number of repetitions were increased depending of toleration of participants. After tenth session step bench jumping exercise and after fifteenth session diagonal jumping exercise were added and study was completed in eighteen session.

In IG, isokinetic exercises were performed by using a Cybex Norm isokinetic dynamometer with an incorporated trunk flexion/extension unit in a standing position. Range of motion was set from 10 degree extension to 40 degree flexion. Each session was consisted warm-up, isokinetic exercises and cool-down periods. Warm-up and cool-down periods were consisted trunk exercise and stretching. Isokinetic exercises were performed 7 repetitions at angular velocity of 90 degree per second , 6 repetitions at angular velocity of 75 degree per second and 5 repetitions at angular velocity of 60 degree per second.

Participants in CG were assessed baseline and at sixth week.

Study Type

Interventional

Enrollment (Actual)

26

Phase

  • Not Applicable

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

35 years to 50 years (ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  • Premenopausal women aged 35-50 years

Exclusion Criteria:

  • to have cardiovascular, musculoskeletal and neurologic disease
  • have been involved in exercise studies within the last 6 months
  • to being receive hormone replacement therapy

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: OTHER
  • Allocation: NON_RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Plyometric Exercise Group
Plyometric exercise training 3 days a week for 6 weeks
ACTIVE_COMPARATOR: Isokinetic Exercise Group
Isokinetic exercise training 3 days a week for 6 weeks
NO_INTERVENTION: Control Group
no exercise intervention

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Isokinetic testing trunk flexion-extension
Time Frame: Six weeks
changes trunk flexion and extension muscle strength from baseline at 6 weeks
Six weeks
Isokinetic testing hip abduction-adduction
Time Frame: Six weeks
changes hip abduction and adduction muscle strength from baseline at 6 weeks
Six weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Beck Depression Inventory
Time Frame: Six weeks
changes inventory scores from baseline at 6 weeks
Six weeks
State Trait Anxiety Inventory
Time Frame: Six weeks
changes inventory scores from baseline at 6 weeks
Six weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Collaborators

Investigators

  • Study Director: Safinaz Yildiz, Istanbul University
  • Study Chair: Turker Sahinkaya, Istanbul University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

January 1, 2006

Primary Completion (ACTUAL)

February 1, 2007

Study Completion (ACTUAL)

May 1, 2007

Study Registration Dates

First Submitted

February 17, 2021

First Submitted That Met QC Criteria

March 18, 2021

First Posted (ACTUAL)

March 22, 2021

Study Record Updates

Last Update Posted (ACTUAL)

March 22, 2021

Last Update Submitted That Met QC Criteria

March 18, 2021

Last Verified

March 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • Kubra2

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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