Shoulder Functional Performance After Shoulder Surgery

A

Abant Izzet Baysal University

Status

Completed

Conditions

Rotator Cuff Tears

Treatments

Other: Shoulder Performance Test- Functional Impairment Test-Head and Neck, Shoulder, Arm (FIT-HaNSA)

Study type

Observational

Funder types

Other

Identifiers

NCT04388306
AIBU-FTR-BYD-01

Details and patient eligibility

About

Rotator Cuff (RC) injuries are a progressive clinical condition that starts with an acute tendonitis, continues with partial thickness rupture and results in a full thickness rupture in the advanced period. Arthroscopic RC repair is effective in the acute RC ruptures treatment caused by traumatic events. In the acute period after arthroscopic RC repair, shoulder joint range of motion (ROM), muscle strength and shoulder functionality are decreased and daily activities are adversely affected. In the long-term, many studies have reported that these symptoms gradually decreaced. Many studies investigating postoperative treatment of RC rupture have mostly focused on parameters such as postoperative pain, functionality, muscle strength, ROM and quality of life.Evaluation of these clinical parameters is necessary for patient follow-up in the early period. However, it is unclear whether the biomechanical etiologic factors continue that lead to RC rupture in the advanced period after surgery. Therefore, the objective of this study was functional performance of shoulder after arthroscopic Rotator Cuff repair and ınvestigation of performance related factors.

Full description

Design: observational Cross-sectional study.

Enrollment

64 patients

Sex

All

Ages

40 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • With the same RC surgical procedure and technique,
  • With acromioplasty and/or tenodesis with RC repair,
  • Undergoing arthroscopic RC repair from the upper extremity of the dominant side,
  • Having completed the 12th week after surgery,
  • Performing 90° and above active shoulder elevation movement

Exclusion criteria

  • Having undergone revision surgery or previous shoulder surgery, a history of fracture of the upper extremity
  • Having undergone surgery causing limitation of motion in the spine,
  • Having a neurological and/or vestibular and/or rheumatologic disease,
  • Participants with diabetes mellitus, hypertension, cardiovascular and chronic respiratory disease that may cause problems during the test

Trial design

64 participants in 2 patient groups

Study Group
Description:
Thirty-two participants with undergone arthroscopic Rotator Cuff repair
Treatment:
Other: Shoulder Performance Test- Functional Impairment Test-Head and Neck, Shoulder, Arm (FIT-HaNSA)
Control Group
Description:
Thirty-two healthy participants
Treatment:
Other: Shoulder Performance Test- Functional Impairment Test-Head and Neck, Shoulder, Arm (FIT-HaNSA)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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