Mobilization With Movement for Shoulder Impingement

Not Applicable

Completed

• Conditions: Shoulder Impingement Syndrome

• Registration Number: NCT02172079
• Lead Sponsor: César Fernández-de-las-Peñas

Brief Summary

Controversy exists regarding the effectiveness of manual therapy techniques for the management of impingement syndrome. However, no adequately powered clinical trials have examined the effects of mobilization-with-movement. The purpose of the current study was to perform a randomized controlled trial comparing the effects of real MWM to a group receiving a sham intervention on shoulder pain at different moments and active shoulder range of motion in an adequately powered sample of patients with shoulder impingement syndrome.

Detailed Description

Not available

Study Timeline

• Study Start: 2013-01
• Primary Completion: 2014-01
• Study Completion: 2014-01
• Status Verified: 2014-06
• Study First Submitted: 2014-06-22
• Study First Submitted QC: 2014-06-23
• Last Update Submitted: 2014-06-23
• Study First Posted: 2014-06-24
• Last Update Posted: 2014-06-24

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 42

Inclusion Criteria

• history of shoulder pain of > 3months duration
• pain localized at the proximal anterolateral shoulder region
• medical diagnosis of shoulder impingement syndrome
• at least 2 positive impingement tests including Neer, Hawking, or Jobe test

Exclusion Criteria

• diagnosis of fibromyalgia
• pregnancy
• a history of traumatic onset of shoulder pain
• other histories of shoulder injury
• ligamentous laxity based on a positive Sulcus test and apprehension test
• numbness or tingling in the upper extremity
• previous shoulder or cervical spine surgery
• corticosteroid injection on the shoulder within 1 year of the study
• physical therapy 6 months prior to the study

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Changes in the intensity of shoulder pain before and after the treatment	Baseline and one week after intervention	Participants were asked to rate the intensity of their pain using an 11-point numerical pain rating scale (NPRS; 0: no pain; 10: maximum pain) for 3 scores of perceived pain: 1, the intensity of shoulder pain experienced in the last 24h; 2, the intensity of shoulder pain at night; 3, the intensity of shoulder pain during shoulder flexion.

Secondary Outcome Measures

Name	Time	Method
Changes in shoulder range of motion before and after the treatment	Baseline and one week after the intervention	A universal goniometer was used to assess the participant's shoulder range of motion in the following motions: * Pain-free and maximum (painful) range of motion in shoulder flexion; * Pain-free range of motion in shoulder extension; * Pain-free range of motion in shoulder abduction; * Pain-free range of motion in shoulder external rotation; * Pain-free range of motion in shoulder medial (internal) rotation

Trial Locations

Locations (1)

Francisco Alburquerque Sendín; 🇪🇸 Salamanca, Spain