Ignite Creation Date:
2024-10-26 @ 3:38 PM
Last Modification Date:
2024-10-26 @ 3:38 PM
Study NCT ID:
NCT06568796
Status:
COMPLETED
Last Update Posted:
None
First Post:
2024-08-12
Brief Title:
Comparison of the Effects of Trigger Point Ischemic Compression Massage and Focused Extracorporeal Shoch Wave Therapy of the Patients With Lateral Epicondylitis a Randomized Controlled Trial
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Comparison of the Effects of Trigger Point Ischemic Compression Massage and Focused Extracarporeal Shock Wave Therapy on Pain Level Muscle Strength Joint Range of Motion Functionality and Quality of Life in Patients With Lateral Epicondylitis a Randomized Controlled Trial
Status:
COMPLETED
Status Verified Date:
2024-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
To compare the effects of Trigger Point Ischaemic Compression Massage TPICM and Focused Extracarporeal Shock Wave Therapy focused ESWT on pain level muscle strength Joint range of motion functionality and quality of life in patients with lateral epicondylitis LE in a randomised controlled trial
Detailed Description:
The study was planned to include at least 66 patients who presented to the sports medicine clinic of Gülhane Training and Research Hospital with lateral epicondyle pain for at least 2 months were diagnosed with lateral epicondylitis and verbally and in writing declared that they were willing to participate in the study
Patients participating in the study
1 assessment of pain intensity with visual analog scale VAS
2 Evaluation of hand grip strength with jamar hand dynamometer
3 Isokinetic muscle strength assessment of wrist muscles with biodex isokinetic system 3
4 assessment of wrist range of motion with a manual goniometer
5 Function assessment with PRTEE-T
6 DASH questionnaire
7 SF-36 quality of life assessment will be performed before and after treatment
inclusion criteria
1 Male and female individuals aged 18-60 years
2 being diagnosed with lateral epicondilitis
3 volunteering to participate in the study
exclusion criteria from eswt treatment
1 non-cooperation
2 presence of systemic and metabolic diseases
3 malignancy osteoporosis fracture blood clotting disorder pacemaker infection
4 pregnancy
5 utilization of another treatment for lateral epicondylitis during the study period
6 previous invasive treatment with steroids for lateral epicondylitis
7 any treatment for lateral epicondylitis in the last 6 months
Patients participating in the study
1 assessment of pain intensity with visual analog scale VAS
2 Evaluation of hand grip strength with jamar hand dynamometer
3 Isokinetic muscle strength assessment of wrist muscles with biodex isokinetic system 3
4 assessment of wrist range of motion with a manual goniometer
5 Function assessment with PRTEE-T
6 DASH questionnaire
7 SF-36 quality of life assessment will be performed before and after treatment
inclusion criteria
1 Male and female individuals aged 18-60 years
2 being diagnosed with lateral epicondilitis
3 volunteering to participate in the study
exclusion criteria from eswt treatment
1 non-cooperation
2 presence of systemic and metabolic diseases
3 malignancy osteoporosis fracture blood clotting disorder pacemaker infection
4 pregnancy
5 utilization of another treatment for lateral epicondylitis during the study period
6 previous invasive treatment with steroids for lateral epicondylitis
7 any treatment for lateral epicondylitis in the last 6 months
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None