3D Shoulder Kinematics During Throwing-related Movement Patterns Tasks in Upper Extremity Low-to-moderate/Moderate-to-high Loading Conditions

NCT02852785 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 150

Last updated 2021-01-06

No results posted yet for this study

Summary

The main purpose of this study is to characterize and compare the 3D shoulder kinematics bilaterally while performing functional movement patterns tests that hypothetically replicate the 5 main phases of the throwing cycle. The tests are based on diagonal D2 for flexion (early and late cocking of the arm) and D2 for extension (acceleration, deceleration and follow-through of the arm) of the upper extremity of proprioceptive neuromuscular facilitation techniques.

Conditions

  • Shoulder Pain

Interventions

BEHAVIORAL

PNF D2 for flexion; low-to-moderate loading condition

Exposure to upper extremity PNF D2 for flexion during low-to-moderate loading condition

BEHAVIORAL

PNF D2 for flexion; moderate-to-high loading condition

Exposure to upper extremity PNF D2 for flexion during moderate-to-high loading condition

BEHAVIORAL

PNF D2 for extension; low-to-moderate loading condition

Exposure to upper extremity PNF D2 for extension during low-to-moderate loading condition

BEHAVIORAL

PNF D2 for extension; moderate-to-high loading condition

Exposure to upper extremity PNF D2 for extension during moderate-to-high loading condition

Sponsors & Collaborators

  • University of Lisbon

    collaborator OTHER
  • Instituto Politécnico de Leiria

    collaborator OTHER
  • Universidade do Porto

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-07-24
Primary Completion
2021-04-30
Completion
2021-07-31

Countries

  • Portugal

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02852785 on ClinicalTrials.gov