Effect of Progressive Isolated Core Stability Training

January 11, 2022 updated by: Ankara Yildirim Beyazıt University

Effect of Progressive Isolated Core Stability Training on Upper Extremity Physical Performance in Adolascent Female Volleyball Athletes

Forty-two adolescent female volleyball athletes (16.0±1.4 years) were randomly divided into two groups. Group 1 was the training group and, in addition to the routine volleyball training programmes, underwent an 8-week (3 days/week) progressive core stability training programme. Group 2 was the control group and only did routine volleyball training, with no core stability training.

Main outcome measures: Shoulder IR and ER strength, medicine ball throw (MBT), modified push up (MPU) and closed kinetic chain (CKC) upper extremity stability tests were used to evaluate physical performance.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

Most studies have focused on the effects of core stability training on injury prevention and physical performance for the lower extremities . However, little is known about its effect on upper extremity performance. Previous studies suggest that core strengthening could enhance upper extremity physical performance because it might lead to more efficient use of the extremity muscles . Core weakness in overhead athletes with shoulder pain. Insufficient power generation by the core muscles might overload the shoulder girdle to compensate for altered biomechanics during throwing, and this overload made the shoulder prone to sport injuries. A systematic review has suggested, however, that isolated core stability training cannot be the primary component of athletic performance enhancement and that the variability in exercise training protocols, testing methods, study population and sample size among the available studies leads to difficulties in understanding whether or not core stability training enhances physical performance.

There has been no study in the literature investigating the effect of progressive isolated core stability training on upper extremity performance in adolescent overhead athletes. This study therefore sought to investigate the effects of progressive isolated core stability training on shoulder internal (IR) and external rotator (ER) strength and upper extremity physical performance in female adolescent volleyball players. Hypothesized that core stability training would enhance shoulder rotator strength and upper extremity physical performance in these athletes.

Study Type

Interventional

Enrollment (Actual)

42

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

      • Ankara, Turkey
        • Ankara Yildirim Beyazit University,Faculty of Health Sciences, Physiotherapy and Rehabilitation Department

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

12 years to 16 years (Child)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Description

Inclusion Criteria:

- be between the ages of 12 and 16, enrolled in a similar training program and agree to participate in the study

Exclusion Criteria:

  • Having any surgery / serious pathology of the spinal column,
  • Have had a lower / upper extremity injury in the last 3 months,
  • Sports age is less than 5 years,
  • Severe orthopedic / systemic discomfort during training,
  • Absence from training for more than 3 sessions
  • Family disapproval or reluctance to study
  • Minimal Q-DASH score (0-25)

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: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: training group
Group 1 (n=21) was the training group and, in addition to the routine volleyball training programmes, an 8-week (3 days/week) progressive core stability training programme was applied.
The core stability training programme was performed 3 days per week over an 8-week period, and each training session lasted approximately 50 minutes.We created a special programme for our study based on the literature; the core stability training programme was divided into 3 phases: easy(1-2 weeks), moderate(3-5 weeks) and difficult(6-8 weeks In the easy phase(phase1), the athlete was intended to gain sensorimotor control that would ensure the smoothness of the neutral spine during slow movements. The participants learned the hallowing technique and how to use this technique while doing core exercises. In the moderate phase(phase2), muscular neural adaptation and neuromuscular facilitation were targeted with the transition to high threshold strength training.In the last, difficult, phase(phase3), subconscious control of movement was taught using combined movement patterns with the aim of transitioning to functional positions and activities.
No Intervention: control group
Group 2 (n=21) was the control group, and they only engaged in routine volleyball training: no core stability training was given.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from Baseline Shoulder Rotator Muscle Strength at 8 weeks.
Time Frame: before and after treatment (24 sessions, beginning and 8th. weeks)
Isometric shoulder IR and ER strength was measured using a handheld dynamometer (Commander Power Track II, J-Tech, USA). The tests were performed with the athletes in a supine position. The shoulder was positioned at 45° abduction, the elbow was at 90° flexion and the forearm was in the neutral position. The supine position was chosen for the test to minimize compensatory movement of the body. At least one practice trial was given to the subjects to familiarize them with the feel of pushing against the dynamometer. Subjects were oriented to each desired action by the tester. The subject then performed the action until performed correctly.
before and after treatment (24 sessions, beginning and 8th. weeks)
Change from Baseline Upper Extremity Functional Tests at 8 weeks.
Time Frame: before and after treatment (24 sessions, beginning and 8th. weeks)
The participants were positioned prone with hands shoulder width apart with the trunk held in a rigid straight position on the mat. Push-ups were performed through the full range of motion, as quickly as possible. Participants started the test with their elbows fully extended. They then flexed their elbows until the upper arm was parallel to the testing surface. The participants were instructed to limit head and trunk motion and to keep the trunk position straight. The number of push-ups completed in 30 seconds was recorded. Verbal encouragement was consistently given to all participants .
before and after treatment (24 sessions, beginning and 8th. weeks)
Change from CKC upper extremity stability test at 8 weeks.
Time Frame: before and after treatment (24 sessions, beginning and 8th. weeks)
This test was performed in a modified push-up test position. There were two lines on the floor, 30 cm apart. The participants were instructed to move their hands back and forth from each line as many as possible for 15 seconds. The number of touches for each line was counted. The test was repeated 3 times, with a 2-minute rest between each trial and the average of the touches was calculated. The final score was calculated as the average number of touches/height
before and after treatment (24 sessions, beginning and 8th. weeks)
Change from MBT test at 8 weeks.
Time Frame: before and after treatment (24 sessions, beginning and 8th. weeks)
The examiner used a marked line on the floor as the starting reference for this test. A mat was placed on the floor and the front of the mat was aligned with the reference line. The participants were instructed to tall kneel (90° knee flexion and neutral trunk position) on the front of the mat with the medicine ball (1.9 kg) held at their chest level against the chest wall. From this position the participants were instructed to throw the medicine ball, using a 2-handed chest pass technique, as far as they could. To minimize momentum, the participants were not allowed to rock back before beginning the throw. The first contact site of the ball was marked, and the throw distance was measured using tape. The test was repeated 3 times, and the average of the throw distances was calculated
before and after treatment (24 sessions, beginning and 8th. weeks)

Collaborators and Investigators

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

Investigators

  • Study Director: Rabia Tugba Kilic, Ankara Yildirim Beyazıt University
  • Principal Investigator: Gülsah Basandac, Yeditepe University Department Of Physiotherapy And Rehabilitation
  • Study Chair: Gülcan Harput, Hacettepe University, Faculty of Physiotherapy and Rehabilitation
  • Study Chair: Volga Bayrakci Tunay, Hacettepe University, Faculty of Physiotherapy and Rehabilitation

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)

September 1, 2012

Primary Completion (Actual)

March 15, 2013

Study Completion (Actual)

June 30, 2013

Study Registration Dates

First Submitted

December 5, 2021

First Submitted That Met QC Criteria

January 11, 2022

First Posted (Actual)

January 25, 2022

Study Record Updates

Last Update Posted (Actual)

January 25, 2022

Last Update Submitted That Met QC Criteria

January 11, 2022

Last Verified

December 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • LUT 12/57

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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