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Scapular DyskinesisSDNCT06293599

Effect of Scapular Stabilization Exercises Versus Virtual Reality Exercises in Basketball Players With Scapular Dyskinesia

A study testing scapular stabilization exercises, virtual reality exercises and regular routine exercises in people with Scapular Dyskinesis, run by Cairo University.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

this study will be conducted to compare virtual reality and scapular stabilizing exercise among basketball player with scapular dyskinesia on scapular muscle performance, rounded shoulder, pain intensity , disability and hand grip strength Read more about this study

Who is it for?
Ages 20 to 25 years
Conditions the study is for
Scapular Dyskinesis
What is being tested?
scapular stabilization exercises, virtual reality exercises and regular routine exercises
Could I receive a placebo?
No, everyone receives an active treatment
How many people
90 participants
Where
No sites listed yet
Study dates
5 Mar 2024to 30 Jul 2024
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 20 to 25 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • ninety basketball players of both genders.
  • Subjects with age between 20 and 25 years old.
  • Subjects with Body Mass Index (BMI) ranging from 18 to 25 kg/m².

Who cannot join

  • An injury within the four weeks before testing.
  • Upper extremity fractures.
  • Bilateral repetitive strain injuries
  • Osteoarthritis on hand

About this study

this study will be conducted to compare virtual reality and scapular stabilizing exercise among basketball player with scapular dyskinesia on scapular muscle performance, rounded shoulder, pain intensity , disability and hand grip strength

Read the detailed description

Scapular dyskinesia (SD) is an alteration in the normal position or motion of the scapula during coupled scapulohumeral movements. It is lack of control of static or dynamic positioning of the scapula relative to the thorax. It affects from 64% to 100% of patients with shoulder lesions. Scapular dyskinesia is a major etiological factor in overhead athletes' shoulder problems. Virtual Reality (VR) it allows individuals to interact and train with or within interesting and relatively realistic three-dimensional(3D) environments. VR and its simulated environments are well accepted in entertainment and computer game applications. However, what is not as well recognized is that VR offers the opportunity for intensive repetition of meaningful task-related activities necessary for effective rehabilitation. The scapular stabilization exercise in rehabilitation aims to Restore shoulder function; these exercises are a combination of scapular stabilization exercises, rotator cuff strengthening exercises, range of motion (ROM), proprioceptive neuromuscular facilitation (PNF), and stretching exercises. Physiotherapy is the mainstay management for several musculoskeletal disorders. sixty basketball athletes with dyskinesea will be assigned randomly to three equal groups; the first will receive Virtual reality exercise and routine exercise, and the second group will receive Stabilization exercise and routine exercise. and finally, the third group will receive routine exercise only for eight weeks

Being tested
scapular stabilization exercises, virtual reality exercises, regular routine exercises
Keywords
scapular stabilization, virtual reality, scapular dyskinesia

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • scapular stabilization exercisesOther

    the patients will receive scapular stabilization exercises in the form of scapular orientation exercises,Forward/Backward Bear Crawls,Lateral Bear Crawls and assisted stretch for pectoralis minor

  • virtual reality exercisesOther

    The exercises described were done in a consistent manner, emphasizing low intensity, and using lightweight dumbbells (range, 3 to 30 pounds). The weight of the dumbbell was individually selected by the subject for each exercise.

    1. elevation of the arm in the sagittal plane (shoulder flexion
    2. elevation of the arm in the scapular plane with humeral external rotation (shoulder scaption
    3. elevation of the arm in the coronal plane (shoulder abduction)
    4. rowing
    5. horizontal shoulder abduction
    6. horizontal abduction with humeral external rotation
    7. push-up with hands apart
    8. push-up with a plus-normal push-up adding maximum shoulder and scapular protraction with elbows fully extended
    9. dumbbell bench press
    10. dumbbell military press
    11. shoulder shrug
    12. deceleration exercise-simulating the pitching followthrough
    13. shoulder extension prone
    14. shoulder internal rotation
    15. shoulder external rotation
    16. press-up
  • regular routine exercisesOther

    the patients will receive routine exercises in the form of Sleeper Stretch: Posterior Capsular Stretch, Push up, Wall slides, Kettlebell High Pull,

Study groups in NCT06293599
Study groupRoleWhat they receive
scapular stabilization exerciseExperimentalthirty patients with scapular dyskinesia will receive scapular stabilization exercise and regular routine three times a week for eight weeks
Receives: Other: scapular stabilization exercises; Other: regular routine exercises
virtual reality exerciseExperimentalthirty patients with scapular dyskinesia will receive virtual reality exercise and regular routine three times a week for eight weeks
Receives: Other: virtual reality exercises; Other: regular routine exercises
Regular routine exerciseActive comparatorthirty patients with scapular dyskinesia will receive regular routine exercises three times a week for eight weeks
Receives: Other: regular routine exercises

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. agonist antagonist ratio

    isokinetic Biodex 3 dynamometer will be used to assess agonist antagonist ratio

    Measured: up to eight weeks

Secondary outcomes (8)
  1. Hand grip strength

    Jamar handheld dynamometer will be used to assess hand grip strength

    Measured: up to eight weeks

  2. rounded shoulder posture

    Patient is supine with the arms at the sides, elbows extended, palms upward, knees bent and lower back flat on the table. The examiner stands at the head of the table and use tape measurements to measure the distance between the acromion of the shoulder joint and the table surface three times. The numbers were averaged and used for analysis. Increased distance signifies higher rounded shoulder posture severity

    Measured: up to eight weeks

  3. pain intensity level

    Visual Analogue Scale (VAS) will be used to assess pain by Using a ruler, the score is determined by measuring the distance on the 10-cm line between the "no pain" anchor and the patient's mark, providing a range of scores from 0-10. A higher score indicates greater pain intensity.

    Measured: up to eight weeks

  4. The disabilities of the arm, shoulder and hand

    The disabilities of the arm, shoulder and hand (DASH) questionnaire will be used to assess the disability in arm, shoulder and hand. The DASH consists mainly of a 30- item disability/symptom scale. The possible score ranges from 0 to 100 points. 0 points represent a complete, unrestricted function of the upper extremities, while 100 points represent the greatest possible functional impairment.

    Measured: up to eight weeks

  5. peak force

    isokinetic Biodex 3 dynamometer will be used to assess peak force

    Measured: up to eight weeks

  6. total work

    isokinetic Biodex 3 dynamometer will be used to assess total work

    Measured: up to eight weeks

  7. work fatigue

    isokinetic Biodex 3 dynamometer will be used to assess work fatigue

    Measured: up to eight weeks

  8. average power

    isokinetic Biodex 3 dynamometer will be used to assess average power

    Measured: up to eight weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted5 Mar 2024
  2. Study start5 Mar 2024 (estimated)
  3. Primary completion30 Jul 2024 (estimated)
  4. Study completion30 Jul 2024 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
scapular stabilization and virtual reality exercise
Masking
Double blind
Who is masked
Investigator, Outcomes assessor
Enrolment
90 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06293599
Sponsor's protocol ID
P.T.REC/012/003131
Acronym
SD
Status last verified
Feb 2024
First submitted
31 Jan 2024
Last updated
5 Mar 2024
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing scapular stabilization exercises, virtual reality exercises and regular routine exercises in people with Scapular Dyskinesis, run by Cairo University.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 5 Mar 2024. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

agonist antagonist ratio (time frame: up to eight weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 Mar 2024.

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