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Shoulder PainNCT02852746

Physical/Self-perceived Performance and 3D Shoulder Kinematics of Volleyball Attackers With/Without Shoulder Complaints and Scapular Dyskinesis

An observational study of Shoulder Pain, run by Universidade do Porto at 3 sites in Portugal.

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 The sponsor has not verified this record for over two years, so it may be out of date.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

The study aims to compare the performance and the 3D shoulder kinematics of volleyball attackers with and without scapular dyskinesis and shoulder symptoms in two physical performance measures of the upper extremity, and correlate their outcomes with a self-reported measure of function of the upper extremity. Read more about this study

Who is it for?
Ages 18 to 40 yearsHealthy volunteers can take part
Conditions the study is for
Shoulder Pain
What is being tested?
Performance measures of the upper extremity
How many people
60 participants
Where
3 sitesPortugal
Study dates
24 Jul 2018to Jul 2021
Phase
Observational
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 18 to 40 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Study population: Athletes from sports organizations involved in competitive events with pain and disability in the shoulder region

Who may be able to join

  • subjects who can perform at least 150 degrees of arm elevation

Who cannot join

  • subjects rating pain ≥8/10
  • score 5 on any of the items of the DASH
  • pain elicited by provocation maneuvers of the neighboring regions (e.g., cervical spine).

Trial locations and contacts

3 sites in 1 country.

Portugal3 sites
  • Escola Superior de Saúde, Instituto Politécnico de Leiria

    Leiria, 2411-901

  • Faculdade de Motricidade Humana, Universidade de Lisboa

    Oeiras, Cruz-Quebrada, 1499-002

  • Faculdade de Desporto, Universidade do Porto

    Porto, 4200-450

Other trials in Portugal

About this study

The study aims to compare the performance and the 3D shoulder kinematics of volleyball attackers with and without scapular dyskinesis and shoulder symptoms in two physical performance measures of the upper extremity, and correlate their outcomes with a self-reported measure of function of the upper extremity.

Read the detailed description

Volleyball attackers with clinically identified scapular dyskinesis and with/without shoulder symptoms will be compared with respect to performance outcomes and scapular kinematics.

Performance will be assessed by means of the unilateral seated shot put test (USSPT), the upper quarter Y balance test (UQYBT), and Disabilities of the Arm, Shoulder and Hand, sports module (DASH). Pain measurements after completing physical performance measures will be assessed and rated. Relationships between physical (USSPT, UQYBT) and self-perceived (DASH) measures of performance, and with impairment-based measures (clinical measures and 3D shoulder kinematics) will be assessed.

Conditions
Shoulder Pain
Being tested
Performance measures of the upper extremity
Medical subject headings
Shoulder Pain

What participants receive

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

  • Performance measures of the upper extremityBehavioural

    Athletes will perform the unilateral seated shot put test (USSPT) and the upper quarter Y balance test (UQYBT) bilaterally.

Study groups in NCT02852746
Study groupRoleWhat they receive
Asympt. athletes / scapular dyskinesisAsymptomatic volleyball attackers involved in competitive events ≥ 2 years and with clinical evidence of scapula dyskinesis
Receives: Behavioral: Performance measures of the upper extremity
Symptom. athletes / scapular dyskinesisSymptomatic volleyball attackers involved in competitive events ≥ 2 years and with clinical evidence of scapula dyskinesis
Receives: Behavioral: Performance measures of the upper extremity

What is being measured

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

  1. Side-to-side differences in the unilateral seated shot put test (normalized distance thrown, in centimeters)

    The unilateral seated shot put test consists of pushing (not throwing) at shoulder height a ~3kg medicine ball as far and forward as possible while keeping the axial skeleton in contact with a wall, knees bent at a right angle, feet flat on the floor, and the non-testing arm resting on the lap.

    Measured: Through study completion, an average of 1 year

  2. Side-to-side differences in the upper quarter Y balance test (normalized maximal distance reached in each direction, in centimeters)

    The upper quarter Y balance test is performed through the assistance of a testing device (Y-Balance Test Kit), with the subject stabilizing his/her body weight with the upper extremity being tested while performing maximal reaching efforts with the free hand in three directions: medial, superolateral, and inferolateral.

    Measured: Through study completion, an average of 1 year

  3. Disabilities of the Arm, Shoulder and Hand (sports module)

    A self-reported measure of upper extremity functioning

    Measured: Through study completion, an average of 1 year

Secondary outcomes (6)
  1. Side-to-side differences in 3-dimensional scapular angular displacement (in degrees)

    The angular displacement of the scapula in the 3 planes of orientation: lateral/medial (upward/downward) rotation, protraction/retraction (internal/external rotation), anterior/posterior tilting.

    Measured: Through study completion, an average of 1 year

  2. Side-to-side differences in 3-dimensional humerus angular displacement (in degrees)

    The angular displacement of the humerus in the 3 planes of orientation: plane of elevation, elevation/depression, axial rotation.

    Measured: Through study completion, an average of 1 year

  3. Side-to-side differences in 3-dimensional thoracic angular displacement (in degrees)

    The angular displacement of the thorax in the 3 planes of orientation: flexion/extension, lateral rotation (inclination), axial rotation.

    Measured: Through study completion, an average of 1 year

  4. Visual Numeric Rating Scale score (0-10)

    A 11-point scale to rate pain intensity

    Measured: Through study completion, an average of 1 year

  5. Side-to-side differences in the upper quarter Y balance test (total excursion, in centimeters)

    total excursion = sum of the 3 normalized reach distances, in centimeters

    Measured: Through study completion, an average of 1 year

  6. Side-to-side differences in the upper quarter Y balance test (overall performance score, in centimeters)

    overall performance or composite score = average score of the 3 normalized reach distances, in centimeters.

    Measured: Through study completion, an average of 1 year]

Timeline

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

  1. First posted2 Aug 2016 (estimated)
  2. Study start24 Jul 2018
  3. Primary completionApr 2021 (estimated)
  4. Study completionJul 2021 (estimated)

Resources

More details

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

Study design
Study type
Observational
Observational model
Case-control
Time perspective
Cross-sectional
Enrolment
60 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02852746
Sponsor's protocol ID
FADEUP_PhDPT_NunoMorais_std#2
Status last verified
Jan 2021
First submitted
25 Jul 2016
Last updated
6 Jan 2021
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

An observational study of Shoulder Pain, run by Universidade do Porto at 3 sites in Portugal.

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 1 inclusion and 3 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 6 Jan 2021. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 3 sites in Portugal. Whether a site is taking part right now should be confirmed with that site. See every site.

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?

Side-to-side differences in the unilateral seated shot put test (normalized distance thrown, in centimeters) (time frame: Through study completion, an average of 1 year). The study lists 3 primary outcomes in all. 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 6 Jan 2021.

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