Effects of Dry Needling, Static Stretching and IASTM in People With Hamstring Muscle Shortness

Gazi University

Status: Completed

Conditions: Hamstring Muscle Shortness and Elastographic Examination

Treatments: Other: Dry needling

Study type: Interventional

Funder types: Other

Identifiers

NCT04118231

2019-114

Details and patient eligibility

About

The aim of this study was to investigate the effects of dry needling, static stretching and instrument assisted soft tissue mobilization on joint range of motion, performance and muscle structure in individuals with Hamstring muscle shortness and to examine the changes in soft tissue before and after application with the help of ultrasound elastography.

Full 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.

Enrollment: 60 patients

Sex: All

Ages: 18 to 80 years old

Volunteers: Accepts Healthy Volunteers

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

Trial design

Primary purpose: Health Services Research

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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60 participants in 2 patient groups

Dry needling

Experimental group

Treatment:

Other: Dry needling

Control group

No Intervention group