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Completed

NCT Number: NCT03186287

Effectiveness of Eccentric and Concentric Strength Training in Patients With Subacromial Impingement Syndrome

The purpose of this study is to investigate and compare the effects of eccentric and concentric strength training on pain, strength, joint position sense and function in patients with subacromial impingement syndrome.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Dokuz Eylul University, School of Physical Therapy and Rehabilitation

Izmir, Balçova, 35340, Turkey (Türkiye)

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosis of subacromial impingement syndrome
  • Complaints associated with subacromial impingement syndrome for at least 3 months
  • No extra pain with 90 degree abduction-90 degree external rotation position of the shoulder
  • Ability to complete the entire study procedure

Exclusion criteria

  • Severe pain; shoulder pain is > 7/10
  • History of upper extremity fracture
  • History of shoulder, cervical and thoracic surgery
  • Having shoulder instability or frozen shoulder diagnosis
  • History of shoulder injuries, trauma and / or shoulder symptoms requiring treatment during the last 1 year (except than subacromial impingement syndrome)
  • Full-thickness rotator cuff tear
  • Systemic musculoskeletal disease
  • Neck and shoulder pain with cervical spine movement
  • Chest deformity or scoliosis diagnosis

Treatment and study plan

Eccentric training

Other

Eccentric phase of resistive shoulder exercises will be performed three sets of 15 repetitions once a day for 12 weeks using therabands. Participants will be supervised by the physiotherapist 3 days a week for the first 6 weeks, 2 days a week for the next 3 weeks and 1 day a week for the last 3 weeks.

Concentric training

Other

Concentric phase of resistive shoulder exercises will be performed three sets of 15 repetitions once a day for 12 weeks using therabands. Participants will be supervised by the physiotherapist 3 days a week for the first 6 weeks, 2 days a week for the next 3 weeks and 1 day a week for the last 3 weeks.

Standard Physiotherapy

Other

The participants will receive standard physiotherapy. The standard physiotherapy exercises will be supervised by the physiotherapist, same as intervention exercises.

Primary outcomes

  1. Shoulder Function

    Time frame: Baseline, 12 weeks and 24 weeks

    Change of Constant Murley Score

Secondary outcomes

  1. Pain intensity

    Time frame: Baseline, 12 weeks and 24 weeks

    Change of visual analog scale score in activity and rest

  2. Upper extremity function

    Time frame: Baseline, 12 weeks and 24 weeks

    Change of disabilities of the arm, shoulder, and hand (DASH) score

  3. Isometric strength

    Time frame: Baseline, 12 weeks and 24 weeks

    Change of shoulder abduction and external rotation isometric strength (in kg, with hand held dynamometer)

  4. Eccentric strength

    Time frame: Baseline, 12 weeks and 24 weeks

    Change of shoulder abduction and external rotation eccentric strength (in kg, with hand held dynamometer)

  5. Joint position sense

    Time frame: Baseline, 12 weeks and 24 weeks

    Change of shoulder joint repositioning angle errors (with bubble inclinometer)

Sponsors and collaborators

Lead sponsor

Dokuz Eylul University

Other

Registry information

Official study title

Effectiveness of Eccentric and Concentric Strength Training in Patients With Subacromial Impingement Syndrome: A Randomized Controlled Trial

Important dates

Study start
2017
Primary completion
2020
Study completion
2020
First posted
Jun 14, 2017
Registry last updated
Apr 17, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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