- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05750550
Acute Effect of Instrument-Assisted Soft Tissue Mobilization on Hamstring Flexibility Via Fascial Chain
September 11, 2023 updated by: Erkan Erol, Tokat Gaziosmanpasa University
Instrument assisted soft tissue mobilization (IASTM) is one of the methods used to achieve fascial release.
In this study, it will be examined whether there will be an increase in hamstring flexibility by releasing the superficial posterior fascial chain as a result of the IASTM technique to be applied over the triceps surae muscle and plantar fascia.
Sociodemographic information of individuals who meet the inclusion criteria and volunteer to participate in the study will be obtained, and straight leg lift test and popliteal angle measurement will be performed with the digital inclinometer (Baseline Digital Inclinometer) to be provided within the scope of the project to measure hamstring flexibility.
Then, IASTM will be applied to the triceps surae muscle and plantar fascia for 15 minutes.
Measurements will be repeated after the application.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
35
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Tokat, Turkey, 60250
- Faculty of Health Sciences, Tokat Gaziosmanpaşa University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Healthy individuals with a straight leg lift test less than 80° and a popliteal angle greater than 15° will be included in the study.
Exclusion Criteria:
- Individuals with a history of lower extremity fractures, lumbar disc herniation, acute pain, a history of lesion in the hamstring muscles at least 1 month before the study, knee or hip prosthesis, and those using drugs that may affect the measurements (e.g., muscle relaxants) will not be included in the study.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Instrument Assisted Soft Tissue Mobilization Group
With the IASTM device, application will be made over the skin to the triceps surae muscle and plantar fascia for 15 minutes.
The application will be made in the prone position.
Massage oil will be used to reduce tissue friction before the application.
|
With the IASTM device, application will be made over the skin to the triceps surae muscle and plantar fascia for 15 minutes.
The application will be made in the prone position.
Massage oil will be used to reduce tissue friction before the application.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Straight Leg Raise Test
Time Frame: Baseline
|
Measurements will be made with a digital inclinometer.
In the supine position, the digital inclinometer will be inserted into the tuberositas tibia.
Then, the participant's leg will be passively lifted by the researcher with the knee extended.
The leg will be brought to the point where the tension is felt, where the value on the inclinometer will be recorded.
It will then return to the starting position.
The procedure will be repeated for both legs.
|
Baseline
|
|
Straight Leg Raise Test
Time Frame: 1 hour
|
Measurements will be made with a digital inclinometer.
In the supine position, the digital inclinometer will be inserted into the tuberositas tibia.
Then, the participant's leg will be passively lifted by the researcher with the knee extended.
The leg will be brought to the point where the tension is felt, where the value on the inclinometer will be recorded.
It will then return to the starting position.
The procedure will be repeated for both legs.
|
1 hour
|
|
Popliteal angle test
Time Frame: Baseline
|
In the supine position, the hip and knee will be brought to 90 degrees.
The digital inclinometer will be placed on the tuberositas tibia and the participant will be asked to extend the knee while maintaining the position of the hip.
At the last point, the value on the inclinometer will be recorded.
It will then return to the starting position.
The procedure will be repeated for both legs.
|
Baseline
|
|
Popliteal angle test
Time Frame: 1 hour
|
In the supine position, the hip and knee will be brought to 90 degrees.
The digital inclinometer will be placed on the tuberositas tibia and the participant will be asked to extend the knee while maintaining the position of the hip.
At the last point, the value on the inclinometer will be recorded.
It will then return to the starting position.
The procedure will be repeated for both legs.
|
1 hour
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 30, 2023
Primary Completion (Actual)
May 31, 2023
Study Completion (Actual)
June 30, 2023
Study Registration Dates
First Submitted
February 19, 2023
First Submitted That Met QC Criteria
February 28, 2023
First Posted (Actual)
March 1, 2023
Study Record Updates
Last Update Posted (Actual)
September 13, 2023
Last Update Submitted That Met QC Criteria
September 11, 2023
Last Verified
September 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- GaziosmanpasaU_Erol_06
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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