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Clinical Trials/NCT05213351
NCT05213351
Completed
N/A

Comparison of the Effectiveness of Two Different Exercise Training in Frozen Shoulder Treatment

Istanbul University1 site in 1 country40 target enrollmentApril 25, 2022

Overview

Phase
N/A
Intervention
Not specified
Conditions
Adhesive Capsulitis
Sponsor
Istanbul University
Enrollment
40
Locations
1
Primary Endpoint
Change from baseline The Shoulder Pain and Disability Index at 6th and 8th week
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The aim of this study is to compare the effects of two different exercise programs in patients with frozen shoulders.

Detailed Description

After being informed about the study, all patients giving written informed and meet the inclusion criteria will be randomized a double-blind manner in a 1:1 (participant and investigator) to graded motor imagery or exercise group.

Registry
clinicaltrials.gov
Start Date
April 25, 2022
End Date
July 20, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Zeynal YASACI

Research Assistant

Istanbul University

Eligibility Criteria

Inclusion Criteria

  • Patients aged \>60 years
  • Patients with shoulder pain of at least six months' duration secondary to tendinopathy and/or partial rotator cuff tear;
  • Patients with ability to follow simple orders; iii)
  • Patients with ability to sign to provide informed consent

Exclusion Criteria

  • Normal passive ROM
  • External ROM \< 30
  • To have received treatment (physiotherapy, intra-articular injection, surgery) related to the existing complaint
  • Pain \< 3 according to the numbered pain assessment scale

Outcomes

Primary Outcomes

Change from baseline The Shoulder Pain and Disability Index at 6th and 8th week

Time Frame: Baseline,6th week and 8th week

The Shoulder Pain and Disability Index (SPADI) was developed to measure current shoulder pain and disability in an outpatient setting. The SPADI contains 13 items that assess two domains; a 5-item subscale that measures pain and an 8-item subscale that measures disability.

Secondary Outcomes

  • Change from baseline QuickDASH at 6th and 8th week(Baseline,6th week and 8th week)
  • Change from baseline two-point discrimination at 6th and 8th week(Baseline,6th week and 8th week)
  • Change from Pain Catastrophizing Scale at 6th and 8th week(Baseline,6th week and 8th week)
  • Change from baseline NPRS at 6th and 8th week(Baseline,6th week and 8th week)
  • Change from baseline range of motion at 6th and 8th week(Baseline,6th week and 8th week)
  • Change from SF-12 at 6th and 8th week(Baseline,6th week and 8th week)

Study Sites (1)

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