Vibration Exercise in the treatemnt of Shoulder Adhesive Capsulits - an Integrated Therapeutic concept

Not Applicable

• Conditions: Adhesive capsulitis, shoulder; M25.6; Stiffness of joint, not elsewhere classified

• Registration Number: DRKS00012742
• Lead Sponsor: Klinische Studieneinheit, Orthopädische Klinik, Universität Würzburg

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2017-07-13
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 25

Inclusion Criteria

• Diagnosis of adhesive Capsulitis
• Age = 18 years
• Functional limitation (Constant-Score, Range of Motion)
• Limited range of motion in glenohumeral joint: external rotation =30°, abduction =90°

Exclusion Criteria

• Surgery at index shoulder within = 56 Tage before enrollement
• Neurologically ascertained plexus lesion
• Endoprostetic joint replacment at the index shoulder
• Non-healed fracture of humerus or scapula at the affected shoulder
• Other medical reasons that according to the investigators assessment might impose an increased risk for the patient

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Functional improvement of affected shoulder comparing both interventions at 18 weeks. Quantitative assessment is performed by means of the Constant-ScoreV at 9 weeks (interim analysis) and 18 weeks (final assessment).

Secondary Outcome Measures

Name	Time	Method
I) Range of motion for abduction, adduction, internal-/external rotation, anteversion and retroversion<br>II) Subjective perception of symptoms using ADL- and DASH-Score<br>III) Pain, assessed via VAS-Score<br>IV) Correlation of outcome measures with data obtained in clinical routine settings<br>V) Consumption of analgesics<br><br>Assessments will be performed at 9 weeks (Interim analysis) und 18 weeks (final assessmet)