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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05683275
Other study ID # KaratayUH6
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 28, 2022
Est. completion date March 7, 2023

Study information

Verified date December 2022
Source KTO Karatay University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Pain, decreased grip strength, and loss of function are observed in individuals with lateral epicondylitis. The aim of this study is to investigate the effects of ESWT and IASTM applications on pain, grip strength and function in individuals with lateral epicondylitis.


Description:

The study will be carried out on volunteers after the approval of the ethics committee. Before the research, individuals and / or their relatives will be informed about the purpose and content of the study. Participants will be randomly divided into three groups: IASTM, ESWT and home exercise group. In addition to home exercise, IASTM and ESWT groups will be given 2 sessions per week for 4 weeks. Pain, grip strength and functionality of the participants will be evaluated before the application, after 4 weeks of application and 4 weeks after the end of the application.


Recruitment information / eligibility

Status Completed
Enrollment 45
Est. completion date March 7, 2023
Est. primary completion date March 7, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: - being diagnosed with chronic LET by a physician - visual analog scale (VAS) pain score = 3 Exclusion Criteria: - any accompanying pathology in the wrist and forearm, such as a fracture or dislocation of the elbow; - treatment with corticosteroid injections in the past 6 months

Study Design


Related Conditions & MeSH terms


Intervention

Other:
IASTM
IASTM will be applied to the affected extremity twice a week for 4 weeks, in total 8 sessions. Participants will be asked to sit comfortably in a chair with back support. IASTM will be applied to the wrist extensor muscles of the participants for 90 seconds in the position where the muscle is tense, with a frequency of 60 beats per minute.
ESWT
ESWT will be applied to the affected elbow two days a week for 4 weeks, a total of 8 sessions, each session 2000 shock 10 Hz frequency, 2.5 bar intensity point and circumferential application.
Home Exercise
Special static stretching and eccentric strengthening exercises for the forearm muscles will be taught and they will be asked to perform 2 sets (morning-lunch-evening) 10 repetitions per day, 5 days a week, for 4 weeks.

Locations

Country Name City State
Turkey KTO Karatay University Konya Karatay

Sponsors (1)

Lead Sponsor Collaborator
KTO Karatay University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change from Baseline Pain assessed by Visual Analog Scale. Pain will be evaluated with Visual Analog Scale. 0 means no pain, 10 means unbearable pain. Baseline, 4 weeks
Secondary Grip strength Grip strength will be evaluated with Hand Dynamometer Baseline, 4 weeks
Secondary Function assessed by Patient-rated Forearm Evaluation Questionnaire Function will be evaluated with Patient-rated Forearm Evaluation Questionnaire Baseline, 4 weeks
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