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Investigation of the Efficacy of Telerehabilitation in Patients With Rotator Cuff Tendinopathy

Investigation of the Efficacy of Telerehabilitation in Patients With Rotator Cuff Tendinopathy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06024551
Enrollment
34
Registered
2023-09-06
Start date
2023-12-15
Completion date
2024-06-15
Last updated
2024-08-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rotator Cuff Injuries, Rotator Cuff Tendinitis

Keywords

rotator cuff tendinopathy, telerehabilitation

Brief summary

The goal of this study is to investigate the effect of telerehabilitation in patients with rotator cuff tendinopathy. The main questions it aims to answer are: * Is telerehabilitation effective in improving the functional status of patients with rotator cuff tendinopathy? * Is telerehabilitation effective in reducing the pain of rotator cuff patients?

Detailed description

Patients between the ages of 18-65 who were diagnosed with rotator cuff tendinopathy will be included in the study. Patients will be divided into two groups. Patients in group 1 will be given a home exercise program. Then, the patients will be called 3 times a week and it will be evaluated whether they do their exercises regularly and whether they do it correctly. At the end of the first month, the patients will be evaluated again for functionality and pain. The patients in group 2 will be given a home exercise program and at the end of the first month, the patients will be evaluated again in terms of functionality and pain.

Interventions

OTHERTelerehabilitation

Patients in this arm will be given telerehabilitation three times a week, for four weeks.

OTHERhome exercise program

Patients in this arm will receive home exercise program for four weeks

Sponsors

Izmir Democracy University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosis of Rotator cuff tendinopathy * Being able to do the prescribed exercises * Having an access to internet and having a computer or smart phone for telerehabilitation

Exclusion criteria

* Patients with a neurological disease that may affect the effectiveness of exercise * History of fracture in shoulder region * History of surgery in shoulder region * Patients with a psychiatric disorder

Design outcomes

Primary

MeasureTime frameDescription
Western Ontario Rotator Cuff Indexone monthWestern Ontario Rotator Cuff Index is a disease-specific quality of life questionnaire, evaluating the change in symptoms and functional ability, specific to a Rotator Cuff tendinopathy. Raw scores range from 0 to 2100 with a higher score indicating decreased quality of life.
Simple Shoulder Testone monthA questionnaire about the function of the involved shoulder. Overall scored is calculated by number of yes/number of completed items. Minimum score is 0 %and maximum is 100 %. Higher scores indicate better function.

Secondary

MeasureTime frameDescription
Range of motionone monthShoulder joint normal range of motion will be measured using a goniometer. Normal movements of the shoulder joint are flexion 180 degrees, abduction 180 degrees, hyperextension 45 degrees, internal rotation 70 degrees and external rotation 90 degrees. Limitations will be evaluated.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026