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Completed

NCT Number: NCT02670174

Influence of Kinetic Chain Training on the Treatment Outcome of Overhead Athletes With Impingement

A randomized controlled trial will be conducted to examine the effectiveness of a traditional home exercise program versus 2 kinetic chain home exercise programs on treatment outcome of overhead athletes with shoulder impingement syndrome. Primary outcome measures are reduction of pain and disability, and improvement in functionality and sports performance. Secondary outcome measures are strength, mobility, flexibility and functional performance.

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Key information

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Vakgroep REVAKI (Ghent University - Ghent University hospital)

Ghent, 9000, Belgium

About this study

Participant are randomly assigned in 3 home exercise groups.

  • The traditional program: consists of solely strengthening the rotator cuff muscles and scapular muscles (e.g. external rotation)
  • Separate kinetic chain program: same exercises as the first group but they also receive an exercise program to separately train the core and lower body. (e.g. external rotation separately and squat separately)
  • Integrated kinetic chain program: same exercises as the first group but all exercises are performed while simultaneously activating the kinetic chain. (e.g. external rotation while squatting).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Symptoms of shoulder impingement on the dominant side for at least 3 months and at least 3 of the following tests are considered positive
  • Jobe
  • Hawkins
  • Neer
  • Painful arc during elevation
  • Pain or lack of force production with isometric external rotation
  • Apprehension test
  • Relocation test
  • Performing overhead sports at least 3 hours/week
  • Shoulder pain interferes with sports activities
  • They have not had treatment for this shoulder pain

Exclusion criteria

  • History of shoulder dislocation or subluxation
  • History of orthopedic surgery
  • No complaints of pain or dysfunction in the upper limb (except impingement related complaints in the dominant shoulder), lower limb or spine at the last 6 months
  • Currently taking nonsteroidal anti-inflammatory medication
  • Received a steroid injection in the past 12 months
  • Participating in another study
  • Known systemic diseases
  • Known structural diseases

Treatment and study plan

Traditional Training

Other

Separate kinetic chain training

Other

Integrated kinetic chain training

Other

Primary outcomes

  1. Changes in Shoulder Pain And Disability Index (SPADI) score

    Time frame: At baseline and within one week after the 6-weeks training program

    Patients will fill in the SPADI questionnaire to evaluate shoulder pain and function. The SPADI is a valid, reliable and frequently used questionnaire for shoulder pain patients consisting of 13 items divided in 2 subscales: pain (5 items) and disability (8 items). Each item was scored on a 10-point numeric rating scale. Total and subscale scores were summed and transformed to a score out of 100 (%) were a higher score indicates a higher level of pain and/or disability

  2. Changes in Western Ontario Shoulder Stability index (WOSI) score

    Time frame: At baseline and within one week after the 6-weeks training program

    The WOSI is a patient-evaluated disease-specific quality of life scoring questionnaire that has been developed for shoulder instability patients. This 21-item questionnaire consists of 4 subscales: physical symptoms (10 items), sport/recreation/work (4 items), lifestyle (4 items), and emotions (3 items). Each item was scored on a 100-mm visual analogue scale. Total and subscale scores were summed and transformed to a score out of 100 (%) where a higher score indicates more limitations in shoulder related quality of life

  3. Subjective perception of shoulder improvement

    Time frame: 6-weeks training program

    A Global Rating of Change (GROC) scale was used to quantify patient-perceived improvement of overall shoulder function after 6 weeks treatment as "improved", "unchanged" or "worse". In case they improved or got worse, the amount of change was reflected on a 5-point scale: very little change, little change, some change, a large change, a very large change. An "unchanged" condition scored 0, "improved" between 1 and 5, and "worse" between -1 and -5 points.

    amount of change was scored on a 5-point scale (very little change, little change, some change, a large change, a very large change)

Secondary outcomes

  1. Changes in shoulder muscle isokinetic strength (Biodex system 4)

    Time frame: at baseline and within one week after the 6-weeks training program

    Isokinetic strength of shoulder internal and external rotators will be measured bilateral with the Biodex device (Biodex system 4, Biodex Medical Systems, Inc., Shirley, New York, USA). For further analysis, concentric peak torque (PT) (rotation) or peak force (PF) (protraction-retraction) values were normalized to body weight (BW). A higher value represents more strength and thus a better outcome.

  2. Changes in shoulder scapular isokinetic strength

    Time frame: at baseline and within one week after the 6-weeks training program

    Isokinetic strength of scapular protraction and retraction muscles will be measured bilateral with the Biodex device (Biodex system 4, Biodex Medical Systems, Inc., Shirley, New York, USA). For further analysis, concentric peak torque (PT) (rotation) or peak force (PF) (protraction-retraction) values were normalized to body weight (BW). A higher value represents more strength and thus a better outcome.

  3. Changes in scapular dyskinesis

    Time frame: at baseline and within one week after the 6-weeks training program

    Scapular dyskinesis will be measured by observing the scapular movement during active elevation. For both sides (left and right), scapular dyskinesis was evaluated as being present or not. In case dyskinesis was present, the amount of dyskinesis is scored as subtle or prominent.

  4. Changes in functional tests for the upper limb measured with the Y Balance Test

    Time frame: at baseline and within one week after the 6-weeks training program

    The YBT-UQ is a commonly used upper extremity functional test to assess closed kinetic chain function of the stance arm while performing an open kinetic chain movement in the reaching arm. Under standardized verbal encouragement, patients stand in a three point plank position while using the free arm to push a reach indicator box as far as possible in 3 reach directions i.e. medial, inferolateral and superolateral.The average of the 3 test trials for each limb and each direction was normalized for upper limb length. Additionally, a normalized composite score per side was calculated by averaging the mean normalized test scores in the 3 reach directions. A higher scores indicates a better outcome.

  5. Return To Play (RTP)

    Time frame: up to one week after the 6-weeks training program

    Is it possible to return to play after 6 weeks intervention or not? In addition, following question was asked: on a scale of 0 to 100%, what is the extent to which the injured shoulder has reached the shoulder function before the injury occurred?

  6. Changes in functional tests for the upper limb measured with the Seated Medicine Ball Throw

    Time frame: at baseline and within one week after the 6-weeks training program

    The SMBT is an open kinetic chain functional screening test to assess bilateral upper body power and strength. The subjects were instructed to sit on the floor with the head, shoulder and back against the wall while holding a 2kg medicine ball with both arms.Participants had to throw the medicine ball forward, in a straight line and as far as possible with head, shoulders and back maintaining full wall contact. For further analysis, the mean distance of 4 test trials was calculated. A higher scores indicates a better outcome.

Sponsors and collaborators

Lead sponsor

University Ghent

Other

Registry information

Official study title

Influence of Kinetic Chain Training on the Treatment Outcome of Overhead Athletes With Shoulder Impingement Syndrome

Important dates

Study start
2015
Primary completion
2018
Study completion
2018
First posted
Feb 1, 2016
Registry last updated
Dec 18, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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