ClinicalTrials.gg
CompletedNCT07572682DNSGyroSHOAUpdated May 7, 2026

Effects of Dynamic Neuromuscular Stabilization (DNS) and Gyrotonic Training on Shoulder Function in Overhead Athletes

An interventional study of Dynamic Neuromuscular Stabilization (DNS) and Gyrotonic Training in Shoulder Injuries, sponsored by Sport University of Tirana. Completed at 1 site in Albania. Open to participants aged 18 Years to 25 Years. Per ClinicalTrials.gov, last updated 2026-05-07.

Sponsored by Sport University of Tirana · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 1 year 2 months after the study started (first participant enrolled Feb 2025, registered Apr 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
90
Allocation
Randomized
Ages
18 Years to 25 Years
Sex
All
01

Study summary

The goal of this randomized control trial is to evaluate the effect of the Dynamic Neuromuscular Stabilization (DNS) and Gyrotonic training compared to a control group on pain level, functional performance, and shoulder stability in overhead athletes aged 18 to 25 years. The main question is whether these interventions are more effective than usual training in improving clinical and performance related outcomes.

Participants will take part in a supervised rehabilitation program based on these methods three times per week for six weeks.

Assessments were performed at baseline and after 6 weeks of intervention. Outcome measures included pain level, functional performance, and dynamic shoulder stability. Also, core endurance, shoulder mobility, and shoulder muscle strength will be evaluated as a secondary outcomes.

These outcomes will be assessed using Visual Analog Scale (VAS), Kerlan-Jobe Orthopedic Clinic score (KJOC), the Y-Balance Upper Quarter Stability Test (UQYBT), McGill Endurance Test Battery, goniometer and digital dynamometer.

The study was approved by the Ethics Committee of the Sports University of Tirana. All participants involved in this study provided written informed consent.

Read the detailed description

One of the most challenging aspects of orthopedic sports medicine is the rehabilitation of the overhead athletes. Overhead athletes place a lot of load on the shoulder joint, because of the volume of throws, mechanical stress and repetitive movements above shoulder level. During the game these athletes require high levels of mobility and stability at the same time, and neuromuscular control. Rapid motion, poor biomechanics, and weak links in the kinetic chain put this area in high risk of injury in glenohumeral joint and surrounding soft tissues. As a result, those athletes are exposed of developing shoulder pain, functional impairments, overuse injuries, and deficits in strength and mobility.

Recent rehabilitation programs for shoulder injuries in overhead athletes incorporate exercise-based interventions that integrate core activation, coordinated movement, and sport-specific function.

The purpose of this randomized controlled trial was to investigate the effect of structured neuromuscular rehabilitation program based on the Dynamic Neuromuscular Stabilization (DNS) method and Gyrotonic training on shoulder pain, functional performance, and dynamic stability in overhead athletes with shoulder injuries. The study looked for to determine whether these interventions could lead to significant improvements in the variables at baseline and after the interventions.

Participants meeting the inclusion criteria were recruited and were randomly allocated into one of three study groups. The intervention consisted of a supervised rehabilitation program focused on key components of shoulder function, such as neuromuscular control, strength, mobility, and coordination. The DNS program was focused on exercise based on developmental kinesiology, aimed to improve core stability, breathing patterns, and shoulder stabilization in various functional positions. The Gyrotonic program incorporated three-dimensional, spiral movement patterns aimed to improve mobility, coordination, and integrated upper limb function. The athletes involved in the DNS and Gyrotonic group continued also with their usual sports training. Exercise sessions were performed regularly in both intervention groups for a period of six-weeks. Participants in the control group continued with the usual training regime and did not receive any specific rehabilitation intervention.

Outcome assessments were conducted at baseline and after six weeks of intervention. Pain intensity, functional performance, dynamic stability were the main outcomes that were evaluated before and after the intervention period.

In addition, core endurance, mobility and muscle strength of glenohumeral joint was evaluated as a secondary outcome before and after the rehabilitation program. This study design allows the comparison of changes over time within and between groups in order to identify the most effective approach for improving pain, functional performance and stability in overhead athletes with shoulder injuries.

The findings of this study aim to provide clinically relevant evidence for the rehabilitation of overhead athletes with shoulder injuries.

02

Conditions studied

  • Shoulder Injuries

Browse trials for

Keywords

  • DNS (Dynamic Neuromuscular Stabilization)
  • Gyrotonic training
  • Shoulder injury
  • Overhead athletes
  • Shoulder Stability
  • Neuromuscular Training
  • Functional Performance
03

In context

Shoulder Injuries

118 studies on the registry are indexed under Shoulder Injuries; 32 are open to participants now.

This study's enrollment of 90 is above the median of 55 across 69 interventional studies indexed under Shoulder Injuries.

Browse Shoulder Injuries studies →

Lead sponsor

Sport University of Tirana is the lead sponsor of 3 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 25 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Male and female participants
  • Had a minimum of two years of sports experience
  • Presence of shoulder region injury or pain
  • Active participation in sports

Exclusion criteria

Exclusion Criteria:

  • Shoulder surgery
  • Neurological disorders that can affect the upper limb
  • Shoulder dislocation
  • Orthopedic condition such as upper or lower limb fractures
  • Athletes with less than two years of sports experience
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
90 participants (actual)

Study arms

  • Experimental
    DNS Group

    Participants involved in DNS group underwent a structured exercise-based intervention aimed to improve mobility, strength, and neuromuscular control. Also, the participants in this group followed the usual training program.

    Other: Dynamic Neuromuscular Stabilization (DNS)

  • Experimental
    Gyrotonic Training Group

    Participants in the Gyrotonic group followed an exercise program based on three-dimensional, flowing movement aimed to improve mobility, strength, and neuromuscular control. Also, the participants continued the usual training program.

    Other: Gyrotonic Training

  • Active comparator
    Control Group

    Participants included in control group continued their usual sports training routines without additional intervention during the study period.

    Other: Usual Training

Interventions

  • OtherDynamic Neuromuscular Stabilization (DNS)

    Dynamic Neuromuscular Stabilization (DNS) The exercise program based on the DNS method was focused on core activation, diaphragmatic breathing, and shoulder stabilization in various positions based on development kinesiology. Sessions were supervised by certificated therapist and were performed three times per week over a period of 6 weeks.

  • OtherGyrotonic Training

    A structured rehabilitation program based on the Gyrotonic method were conducted in the second intervention group. Sessions were supervised by certificated therapist and were conducted three times per week for 6 weeks. The program based on this method was focused on shoulder mobility and stability.

  • OtherUsual Training

    Participants continued their usual sports training without any additional protocol exercise. The inclusion of the control group allows for the assessment of the additional effect of the interventions beyond usual training.

06

What researchers measure

Primary outcomes

  1. Change from baseline in Shoulder Functional Performance (Kerlan-Jobe Orthopaedic Clinic Shoulder and Elbow Score)

    Shoulder functional performance was assessed using the Kerlan-Jobe Orthopedic Clinic Shoulder and Elbow Score Questionnaire (KJOC), a validated 0-100 scale, where higher scores indicate better function. Changes from baseline to post-intervention will be evaluated.

    Time frame: Baseline (pre-intervention) and after 6 weeks of intervention

  2. Change from baseline in Shoulder Pain (Visual Analog Scale)

    Shoulder pain was assessed by Visual Analog Scale (VAS), a 0-10 scale, where higher scores indicate greater pain intensity. Changes from baseline to post-intervention will be evaluated.

    Time frame: Baseline (pre-intervention) and 6 weeks after of intervention.

Secondary outcomes

  1. Changes from baseline in Upper Limb Dynamic Stability (Upper Quarter Y Balance Test)

    Upper limb dynamic stability was assessed by Upper Quarter Y Balance Test (UQYBT), which evaluates reach distance in multiple directions to assess functional shoulder stability. Results were recorded in centimeters and normalized as a percentage of limb length. Higher scores indicates better dynamic stability.

    Time frame: Baseline (pre-intervention) and after 6 weeks of intervention.

  2. Change from baseline in Trunk Flexor Endurance

    Trunk flexor endurance was assessed using the McGill Endurance Battery Test and was recorded in seconds (s). Higher values indicate greater endurance

    Time frame: Baseline (pre-intervention) and after 6 weeks of intervention.

  3. Change from baseline in Trunk Extensor Endurance

    Trunk extensor endurance was assessed by McGill Endurance Battery Test, a validated clinical assessment of trunk muscle endurance. Performance is recorded in seconds. Higher values indicate greater muscular endurance.

    Time frame: Baseline (pre-intervention) and after 6 weeks of intervention.

  4. Change from baseline in Shoulder Abduction Range of Motion

    Glenohumeral abduction range of motion (ROM) was assessed in both upper limbs, the dominant and non-dominant using a universal goniometer in degrees (◦). Goniometer is a validated instrument for joint angle measurement. Higher values indicate greater joint mobility. Changes from baseline to post intervention will be analyzed.

    Time frame: Baseline (pre-intervention) and after 6 weeks of intervention.

  5. Change from baseline in Shoulder Internal Rotation Range of Motion

    Glenohumeral internal rotation range of motion (ROM) was assessed in both upper limbs, the dominant and non-dominant using a universal goniometer in degrees (◦). Goniometer is a validated instrument for joint angle measurement. Higher values indicate greater joint mobility. Changes from baseline to post intervention will be analyzed.

    Time frame: Baseline (pre-intervention) and after 6 weeks of intervention.

  6. Change from baseline in Shoulder External Rotation Range of Motion

    Glenohumeral external rotation range of motion (ROM) was assessed in both upper limbs, the dominant and non-dominant using a universal goniometer in degrees (◦). Goniometer is a validated instrument for joint angle measurement. Higher values indicate greater joint mobility. Changes from baseline to post intervention will be analyzed.

    Time frame: Baseline (pre-intervention) and after 6 weeks of intervention.

  7. Change from baseline in Shoulder Internal Rotation Muscle Strength

    Shoulder internal rotation muscle strength was assessed using a digital dynamometer, a valid and reliable instrument for isometric muscle strength, and expressed in Newton (N). Higher values indicate greater muscle strength.

    Time frame: Baseline (pre-intervention) and after 6 weeks of intervention.

  8. Change from baseline in Shoulder External Rotation Muscle Strength

    Shoulder external rotation muscle strength was assessed using a digital dynamometer, a valid and reliable instrument for isometric muscle strength, and expressed in Newton (N). Higher values indicate greater muscle strength.

    Time frame: Baseline (pre-intervention) and after 6 weeks of intervention.

  9. Change from baseline in Shoulder Abduction Muscle Strength

    Shoulder abduction muscle strength was assessed using a digital dynamometer, a valid and reliable instrument for isometric muscle strength, and expressed in Newton (N). Higher values indicate greater muscle strength.

    Time frame: Baseline (pre-intervention) and after 6 weeks of intervention.

Other outcomes

  1. Change from baseline in Limb Symmetry Index

    Limb symmetry Index (LSI) will be calculated as the ratio of lower performing limb to higher performing limb, multiplied by 100 and expressed as a percentage(%). Values closer to 100% indicate greater inter-limb symmetry.

    Time frame: Baseline (pre-intervention) and after 6 weeks of intervention.

  2. Changes from baseline in Glenohumeral Internal Rotation Deficit (GIRD)

    Glenohumeral Internal Rotation Deficit (GIRD) will be calculate as the difference in shoulder internal rotation range of motion between the dominant and non-dominant shoulders, measured in degrees (◦). Higher values indicate greater internal rotation deficit.

    Time frame: Baseline (pre-intervention) and after 6 weeks of intervention.

  3. Change from baseline in shoulder External to Internal Rotation Strength Ratio

    The external/internal rotation (ER/IR) strength ratio will be calculated as the ratio of isometric external rotation strength to internal rotation strength measured using a digital dynamometer. The ER/IR ratio is unitless, with values of approximately 0.66-0.75 considered normal; values below 0.66 indicate external rotator strength deficit, while values above 0.75 indicate relative external rotator dominance or adaptation.

    Time frame: Baseline (pre-intervention) and after 6 weeks of intervention.

  4. Change from baseline in Trunk Flexor to Extensor Endurance Ratio

    The trunk flexor/extensor endurance ratio will be calculated as flexor endurance time divided by extensor endurance time. The ratio is unitless, with values closer to 1 indicating better muscular balance.

    Time frame: Baseline (pre-intervention) and after 6 weeks of intervention.

07

Study locations

1 site
  • Sport University of Tirana
    Tirana, Tirana 1001, Albania
08

References and documents

Individual participant data

Plan to share: No — The individual participant data (IPD) will not be shared in order to protect participant confidentiality and privacy. In accordance with institutional regulations and informed consent obtained from participants, only overall results will be reported in publications.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 7, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07572682
Lead sponsor
Sport University of Tirana
Responsible party
Jonida Drizaj (Physiotherapist, Assistant Lecturer, PhD Candidate, Sport University of Tirana) — Principal investigator
First posted
May 7, 2026
Start date
Feb 17, 2025
Primary completion
Mar 17, 2025
Completion
Jun 20, 2025
Last update
May 7, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion