NCT07572682

Brief 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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
90

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Feb 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 17, 2025

Completed
28 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 17, 2025

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 20, 2025

Completed
10 months until next milestone

First Submitted

Initial submission to the registry

April 23, 2026

Completed
14 days until next milestone

First Posted

Study publicly available on registry

May 7, 2026

Completed
Last Updated

May 7, 2026

Status Verified

April 1, 2026

Enrollment Period

28 days

First QC Date

April 23, 2026

Last Update Submit

April 30, 2026

Conditions

Keywords

DNS (Dynamic Neuromuscular Stabilization)Gyrotonic trainingShoulder injuryOverhead athletesShoulder StabilityNeuromuscular TrainingFunctional Performance

Outcome Measures

Primary Outcomes (2)

  • 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.

    Baseline (pre-intervention) and after 6 weeks of intervention

  • 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.

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

Secondary Outcomes (9)

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

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

  • Change from baseline in Trunk Flexor Endurance

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

  • Change from baseline in Trunk Extensor Endurance

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

  • Change from baseline in Shoulder Abduction Range of Motion

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

  • Change from baseline in Shoulder Internal Rotation Range of Motion

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

  • +4 more secondary outcomes

Other Outcomes (4)

  • Change from baseline in Limb Symmetry Index

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

  • Changes from baseline in Glenohumeral Internal Rotation Deficit (GIRD)

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

  • Change from baseline in shoulder External to Internal Rotation Strength Ratio

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

  • +1 more other outcomes

Study Arms (3)

DNS Group

EXPERIMENTAL

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)

Gyrotonic Training Group

EXPERIMENTAL

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

Control Group

ACTIVE COMPARATOR

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

Other: Usual Training

Interventions

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.

DNS Group

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.

Gyrotonic Training Group

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.

Control Group

Eligibility Criteria

Age18 Years - 25 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Sport University of Tirana

Tirana, Tirana, 1001, Albania

Location

MeSH Terms

Conditions

Shoulder Injuries

Condition Hierarchy (Ancestors)

Wounds and Injuries

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Masking Details
Outcome assessors will be blinded to group allocation. The assessors performing questionnaires and functional tests will not be informed about whether participants are assigned to DNS group, Gyrotonic training group, or control group. Participants and therapists will be aware of the assigned interventions due to the nature of the rehabilitation methods.
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Participants will be allocated into three parallel groups: DNS intervention group, Gyrotonic intervention group, and control group continued their regular sports training program and did not receive any additional intervention during the study period.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Physiotherapist, Assistant Lecturer, PhD Candidate

Study Record Dates

First Submitted

April 23, 2026

First Posted

May 7, 2026

Study Start

February 17, 2025

Primary Completion

March 17, 2025

Study Completion

June 20, 2025

Last Updated

May 7, 2026

Record last verified: 2026-04

Data Sharing

IPD Sharing
Will not share

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.

Locations