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Investigation of the Effect of Instrument Assisted Soft Tissue Mobilization Technique on Fascia and Fat Tissue Thickness in Healthy Individuals.

Not Applicable
Conditions
Rehabilitation
Flexibility
Balance
Instrument-assisted Soft Tissue Mobilization
Fascia
Strength
Interventions
Other: Observational
Other: IASTM Technique Application
Registration Number
NCT05502497
Lead Sponsor
Inonu University
Brief 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.

Detailed 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 & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
14
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

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Control GroupObservationalWhich leg of the individuals will be treated will be determined by tossing a coin. After the toss, the right leg will be applied when the tail comes, and the left leg will be applied when it comes to the heads. The leg to be treated, the treatment group of the individuals; the other leg (the untreated leg) will form the control group of the individuals.
IASTM Treatment GroupIASTM Technique ApplicationWhich leg of the individuals will be treated will be determined by tossing a coin. After the toss, the right leg will be applied when the tail comes, and the left leg will be applied when it comes to the heads. The leg to be treated, the treatment group of the individuals; the other leg (the untreated leg) will form the control group of the individuals.
Primary Outcome Measures
NameTimeMethod
Fascia and Adipose Tissue Thickness AssessmentControl evaluation 1 hour after the end of treatment (third evaluation).

Ultrasound device will be used to measure the thickness of individuals' fascia and adipose tissue.

Flexibility AssessmentControl evaluation 1 hour after the end of treatment (third evaluation).

The sit-and-reach Test will be used to assess the flexibility of individuals.

Balance AssessmentControl evaluation 1 hour after the end of treatment (third evaluation).

Stork Balance Test will be used to evaluate the balance of individuals.

Leg Muscle Strength AssessmentControl evaluation 1 hour after the end of treatment (third evaluation).

The Vertical Jump Test will be used to evaluate the leg muscle strength of individuals.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Inonu University

🇹🇷

Malatya, Turkey

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