Effects of Exercises on Physical Performance

January 29, 2020 updated by: Özge Gökalp, Eastern Mediterranean University

Effects of Thrower's Ten Exercises on Upper Extremity Strength, Power and Balance

Aim: The aim of the study was to investigate the effects of thrower's ten exercises on the upper extremity performance in healthy sedentary individuals.

Method: 36 healthy sedentary men and women aged 18-35 years will be included in the study. Subjects will be divided into two groups: exercise and control. The exercise group will be given Thrower's Ten training sessions 3 times a week over an 8-week period. Before and after the study, the subjects were tested for dynamic balance on the upper extremity with the Upper Limp Y balance test and for explosive power with the medicine ball throw test. Moreover, the strength of the shoulder rotator muscles was measured with an isokinetic dynamometer at a speed of 60º/sec.

Study Overview

Status

Completed

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

36

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Famagusta, Cyprus, 99628
        • Eastern Mediterranean University

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

18 years to 35 years (ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Healthy women and men aged 18-35 years

Exclusion Criteria:

  • Individuals with any neurological, orthopedic, cardiovascular, psychological problems,
  • individuals who have a musculoskeletal injury in the last 1 year,
  • individuals who doing regular physical activity/sport in the last 6 months

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: SUPPORTIVE_CARE
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Exercise Group
Thrower's ten exercises will given for 8 weeks, 3 days in a week.
Thrower's ten exercises will given for 8 weeks, 3 days in a week.
NO_INTERVENTION: Control Group
Nothing given to the control group, will be told to continue their normal life for 8 weeks.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in the level of upper extremity strength assessed by an isokinetic dynamometer (Cybex Norm).
Time Frame: At the beginning and at the end of 8 weeks.
During all tests, participants will be encouraged verbally and visually. The forces of the upper extremity will be measured with an isokinetic dynamometer and an angular velocity of 5 repetitions at 60 ° / sec. Before the actual exam, subjects will allowed to make 3 trials. The test results will be recorded for the dominant side.
At the beginning and at the end of 8 weeks.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in the level of upper extremity explosive strength assessed by a seated medicine ball throw (SMBT) test.
Time Frame: At the beginning and at the end of 8 weeks.
A line will be drawn on a flat surface before testing. In the beginning, the subject will sits on this line with the head, back, and butt leaning against the wall and legs extending straight following the line. Hands were placed on the two sides of the wall without fingers touching. Upon the start command, the subject will lifted the ball to the chest and threw forwards as in a basketball shot. A 2 kg medicine ball will used in the test.
At the beginning and at the end of 8 weeks.

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in the level of upper extremity balance assessed using Upper Quarter Y Balance Test (UQYBT)
Time Frame: At the beginning and at the end of 8 weeks.
Participants will put the dominant or non-dominant hand to be tested on the starting line and extended the arm in medial, inferior lateral, and superior lateral directions and the length will measured in all 3 directions in cm.
At the beginning and at the end of 8 weeks.

Collaborators and Investigators

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

Investigators

  • Study Chair: Berkiye Kırmızıgil, Asst. Prof, Eastern Mediterranean University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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)

November 18, 2019

Primary Completion (ACTUAL)

January 22, 2020

Study Completion (ACTUAL)

January 29, 2020

Study Registration Dates

First Submitted

November 12, 2019

First Submitted That Met QC Criteria

November 13, 2019

First Posted (ACTUAL)

November 14, 2019

Study Record Updates

Last Update Posted (ACTUAL)

January 30, 2020

Last Update Submitted That Met QC Criteria

January 29, 2020

Last Verified

January 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • 2017/45-03

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

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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