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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05502497
Other study ID # ÜSAME TAS-002
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date April 1, 2021
Est. completion date October 1, 2022

Study information

Verified date August 2022
Source Inonu University
Contact Muhammed Üsame TAS, Lecturer
Phone +90 0534 681 25 85
Email fzt.muhammedusame.tas@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Description:

In the study, iASTM will be applied to healthy individuals and the effect of this technique will be examined. Demographic information of individuals will be recorded; Individuals will be evaluated in detail in terms of muscle strength, flexibility, balance, and fascia and adipose tissue thickness. The work plan; pre-treatment evaluation, followed by treatment, second evaluation immediately after the end of treatment and control evaluation (third evaluation) 1 hour after the end of treatment. The data collection period is planned as 1,5 year.


Recruitment information / eligibility

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.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Observational
No application will be made to the control group.
IASTM Technique Application
Instrument-assisted soft tissue mobilization will be applied to the legs of the individuals to be treated with ultrasound gel for 2 minutes.

Locations

Country Name City State
Turkey Inonu University Malatya

Sponsors (1)

Lead Sponsor Collaborator
Inonu University

Country where clinical trial is conducted

Turkey, 

Outcome

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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