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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04538690
Other study ID # 10840098-722.02
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date September 15, 2020
Est. completion date November 20, 2020

Study information

Verified date October 2020
Source Istanbul Medipol University Hospital
Contact Gizem Ergezen
Phone +905347098414
Email gergezen@hotmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

20 adults who applied to the orthopedic clinic with shoulder pain, did not require surgical intervention, were referred to the physiotherapy clinic for treatment; will be evaluated in terms of balance, pain and joint range of motion and then included in the exercise program. 20 adults without pain will be evaluated as the control group and the results will be compared within and between groups. Our hypothesis is that the balance will improve and pain will decrease in individuals after exercise.


Description:

20 adults who applied to the orthopedic clinic with shoulder pain, did not require surgical intervention, were referred to the physiotherapy clinic for treatment; will be evaluated in terms of balance, pain and joint range of motion and then included in the exercise program. 20 adults without pain will be evaluated as the control group and the results will be compared within and between groups. Exercises will be applied 3 days a week for 4 weeks, 45-55 minutes by a physiotherapist within the framework of shoulder rehabilitation. In addition, balance exercises will not be given. Balance measurements will be made by the Biodex Balance System, which provides objective data.


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date November 20, 2020
Est. primary completion date November 15, 2020
Accepts healthy volunteers No
Gender All
Age group 20 Years to 60 Years
Eligibility Inclusion Criteria:

- Having one of the diagnoses of impingement, rotator cuff syndrome, frozen shoulder, biceps tendon,

- Pain severity felt by the patient above-8 according to the Visual Analogue Scale divided into 10 equal intervals,

- Patients who were recommended conservative treatment

Exclusion Criteria:

- Any previous surgical operation,

- Skeletal system fractures or dislocations,

- Other diagnosed orthopedic, neurological or rheumatological diseases, diabetes, neuropathy and pregnancy

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Shoulder Exercises
Exercises consist of shoulder range of motion, releasing exercises, strength training, stretching.
Electrotherapy
TENS, US

Locations

Country Name City State
Turkey Istanbul Medipol University Istanbul Beykoz

Sponsors (1)

Lead Sponsor Collaborator
Istanbul Medipol University Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Objective Balance Measurement By Biodex Balance System Stability and Fall Risk, static and dynamic 4 week
Primary Pain Intensity By Visual Analogue Scale scored between 0-10. 0 means no pain and 10 means unbearable pain. 4 week
Secondary Range of Motion By Goniometer shoulder range of motion will be measured 4 week
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