Effects of Dry Needling, Static Stretching and IASTM in People With Hamstring Muscle Shortness
Keywords
Abstract
Description
The study was randomly divided into 3 groups. Group 1: Hamstring muscle group of patients for 5 minutes Instrument Assisted Soft Tissue Mobilization made of stainless steel instruments used by soft tissue mobilization by the therapist. In order to reduce friction and increase lubricity before application; If there is an unexpected erythema, edema or other unexpected side effects, the application will be stopped immediately.
2.Group: In the Hamstring muscle group of the patients, the acupuncture needles, which are made of stainless steel, sterile and disposable, will be applied under the supervision of an expert doctor for 30-45 seconds. In case of unexpected side effects, the application will be terminated.
Group 3: Patients' Hamstring muscle group under the supervision of the physiotherapist for a total of 5 minutes; A total of 10 repetitions of static tension will be applied for 30 seconds.
Before starting the study, anthropometric measurements, vertical and horizontal jump amounts of all participants will be measured before the application. Digital inclinometer will be used to determine the range of motion of the joint. Measurements will be made before and after the first application and the last measurement will be made 3 days after the end of 12 sessions. In addition, soft tissue changes in the hamstring muscle of the participants will be evaluated by US elastography before and at the end of the 12th session.
Dates
| Last Verified: | 09/30/2019 |
| First Submitted: | 10/02/2019 |
| Estimated Enrollment Submitted: | 10/03/2019 |
| First Posted: | 10/07/2019 |
| Last Update Submitted: | 10/03/2019 |
| Last Update Posted: | 10/07/2019 |
| Actual Study Start Date: | 09/30/2019 |
| Estimated Primary Completion Date: | 09/30/2020 |
| Estimated Study Completion Date: | 05/31/2021 |
Condition or disease
Intervention/treatment
Other: Dry needling
Phase
Arm Groups
| Arm | Intervention/treatment |
|---|---|
| Experimental: Dry needling | Other: Dry needling Group 1: Dry needling Group 2: static stretching Group 3: IASTM |
| No Intervention: Control group |
Eligibility Criteria
| Ages Eligible for Study | 18 Years To 18 Years |
| Sexes Eligible for Study | All |
| Accepts Healthy Volunteers | Yes |
| Criteria | Inclusion Criteria: 1. 18-35 age range 2. Volunteer to participate in the study 3. Not having a diagnosed condition Exclusion Criteria: 1. Having any diagnosed discomfort 2. Being pregnant 3. Previously undergo surgery on the lower extremity 4. Physical therapy and rehabilitation of lower extremity in the last 6 months |
Outcome
Primary Outcome Measures
1. Range of motion [4 weeks]
2. Muscle Strength [4 weeks]
3. Vertical jump [4 weeks]
4. Muscle stiffness [4 weeks]
