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Investigation of the Effect of Exercise Training on Psychosocial Outcomes in Rotator Cuff Tears

I

Istanbul University - Cerrahpasa (IUC)

Status

Completed

Conditions

Pain, Shoulder
Psychological
Rotator Cuff Tears

Treatments

Diagnostic Test: Home exercise program
Other: Supervised exercise program

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

This study aimed to determine the psychosocial effects of exercise training in patients with rotator cuff tears.

Full description

This study aimed to determine the psychosocial effects of exercise training in patients with rotator cuff tears. Fifty voluntary patients with partial rotator cuff tear will be randomized into two groups: Supervised exercise group (SE) and home exercise (HE) group, for a standardized 8 weeks exercise program. The primary outcome is the Constant-Murley Score (CMS). The secondary outcomes are the Visual Analogue Scale (VAS), active range of motion (AROM), Pain Catastrophizing Scale (PCS), Hospital Anxiety and Depression Scale (HADS), Pittsburgh Sleep Quality Index (PSI), Short Form-12 (SF-12), and Global Rating of Change (GRC). Outcome measures will be performed at baseline and at the end of 8-week intervention.

Enrollment

70 patients

Sex

All

Ages

40 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria: Forty years of age or older patients that have been diagnosed for a partial rotator cuff tear that is unrelated to trauma by a specialist orthopedist with MRI and physical examination and no other shoulder problems on the diagnosed shoulder will be included into this study.

Exclusion Criteria: Patients diagnosed with full-thickness or massive rotator cuff tear, patients who undergone previous surgery, patients diagnosed with frozen shoulder or glenohumeral instability, and athletic patients younger than 40 years of age with symptoms of acute RC tear will not be included into this study.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

70 participants in 2 patient groups

Supervised exercise group
Experimental group
Description:
The group received the supervised exercise program
Treatment:
Other: Supervised exercise program
Home exercise group
Active Comparator group
Description:
The group received the home exercise program
Treatment:
Diagnostic Test: Home exercise program

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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