Rehabilitation Clinical Trial
Official title:
Investigation of the Effect of Instrument Assisted Soft Tissue Mobilization Technique on Strength, Flexibility, Balance and Fascia and Fat Tissue Thickness in Healthy Individuals.
Instrument-assisted soft tissue mobilization (IASTM) technique can be used for non-pathological conditions as it has been shown in previous literature to affect flexibility and normal range of motion. The use of instrument-assisted soft tissue mobilization technique has been claimed to be an effective treatment in increasing tissue temperature, reducing adhesion to connective tissue and increasing collagen adaptation and increasing flexibility and normal range of motion. The instrument-assisted soft tissue mobilization technique works on the facial connective tissue in the body. This connective tissue contains "sheaths of collagen, which form the cavities and muscle divisions that mainly cover the organs." In some studies, they stated that instrument-assisted soft tissue mobilization increased perfusion, while in some studies they stated that instrument-assisted soft tissue mobilization increased blood circulation. The frequency of ultrasonography (USG) examinations for the musculoskeletal system has increased over time with technological developments and USG has entered daily use in the evaluation of various pathological conditions belonging to this system thanks to its comparable results with MR examinations. The unique advantages of USG such as low cost, easy availability, relatively short examination time, and dynamic real-time comparison with the contralateral side have made it easier to use for musculoskeletal examinations. The aim of this study is to investigate the effect of instrument-assisted soft tissue mobilization technique on strength, flexibility, balance, fascia and adipose tissue thickness in healthy individuals.
Status | Recruiting |
Enrollment | 14 |
Est. completion date | October 1, 2022 |
Est. primary completion date | September 1, 2022 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 35 Years |
Eligibility | Inclusion Criteria: 1. Consists of healthy individuals between the ages of 18-35, 2. No history of orthopedic injury (muscle, tendon, joint capsule, ligament damage or peripheral neuropathy) in the lower extremities in the last 1 year, 3. Being able to express himself without cognitive, cognitive and mental problems, 4. Voluntarily agree to participate in the study. Exclusion Criteria: 1. Injury to any lower extremity between measurements during the treatment process, 2. Having a BMI over 25, 3. Surgery or arthritis in the last 1 year, 4. Not being able or unwilling to do the tests, 5. Not wanting to leave of their own accord. |
Country | Name | City | State |
---|---|---|---|
Turkey | Inonu University | Malatya |
Lead Sponsor | Collaborator |
---|---|
Inonu University |
Turkey,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Leg Muscle Strength Assessment | The Vertical Jump Test will be used to evaluate the leg muscle strength of individuals. | Pre-treatment assessment. | |
Primary | Leg Muscle Strength Assessment | The Vertical Jump Test will be used to evaluate the leg muscle strength of individuals. | Second assessment immediately after the end of the 10-minute treatment. | |
Primary | Leg Muscle Strength Assessment | The Vertical Jump Test will be used to evaluate the leg muscle strength of individuals. | Control evaluation 1 hour after the end of treatment (third evaluation). | |
Primary | Flexibility Assessment | The sit-and-reach Test will be used to assess the flexibility of individuals. | Pre-treatment assessment. | |
Primary | Flexibility Assessment | The sit-and-reach Test will be used to assess the flexibility of individuals. | Second assessment immediately after the end of the 10-minute treatment. | |
Primary | Flexibility Assessment | The sit-and-reach Test will be used to assess the flexibility of individuals. | Control evaluation 1 hour after the end of treatment (third evaluation). | |
Primary | Balance Assessment | Stork Balance Test will be used to evaluate the balance of individuals. | Pre-treatment assessment. | |
Primary | Balance Assessment | Stork Balance Test will be used to evaluate the balance of individuals. | Second assessment immediately after the end of the 10-minute treatment. | |
Primary | Balance Assessment | Stork Balance Test will be used to evaluate the balance of individuals. | Control evaluation 1 hour after the end of treatment (third evaluation). | |
Primary | Fascia and Adipose Tissue Thickness Assessment | Ultrasound device will be used to measure the thickness of individuals' fascia and adipose tissue. | Pre-treatment assessment. | |
Primary | Fascia and Adipose Tissue Thickness Assessment | Ultrasound device will be used to measure the thickness of individuals' fascia and adipose tissue. | Second assessment immediately after the end of the 10-minute treatment. | |
Primary | Fascia and Adipose Tissue Thickness Assessment | Ultrasound device will be used to measure the thickness of individuals' fascia and adipose tissue. | Control evaluation 1 hour after the end of treatment (third evaluation). |
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