The Effects of Instrument-Assisted Soft Tissue Mobilization in Sedentary Individuals With Hamstring Tightness

Not Applicable

Completed

• Conditions: Hamstring Muscle Tightness; Muscle Strength; Pain Threshold

• Registration Number: NCT07091383
• Lead Sponsor: Cyprus International University

Brief Summary

The aim of this study will be to investigate and compare the effects of static stretching exercise, Instrument Assisted Soft Tissue Mobilization (IASTM), and functional IASTM techniques on hamstring muscle shortness, pain threshold, skinfold thickness, and functional muscle strength in sedentary individuals. Fifty-one sedentary individuals between the ages of 18 and 45 who meet the inclusion criteria of Cyprus International University will be included in the study. The first group will receive static stretching exercises two days a week for four weeks; the second group will receive the IASTM technique two days a week for four weeks; and the third group will receive the functional IASTM technique, which will be applied with passive movements two days a week for four weeks. Hamstring shortness, pain threshold, skinfold thickness, and functional muscle strength will be evaluated before the treatment (BT), immediately after the treatment (AT1), two weeks after the treatment (AT2), and four weeks after the treatment (AT4).

Detailed Description

Not available

Study Timeline

• Study Start: 2022-04-11
• Primary Completion: 2022-07-02
• Study Completion: 2022-08-03
• Status Verified: 2025-07
• Study First Submitted: 2025-07-22
• Study First Submitted QC: 2025-07-22
• Last Update Submitted: 2025-07-22
• Study First Posted: 2025-07-29
• Last Update Posted: 2025-07-29

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 51

Inclusion Criteria

• Sedentary individuals aged 18 to 45
• Who worked at a desk for extended periods
• Who exhibited hamstring muscle tightness of more than 10 degrees

Exclusion Criteria

• Diagnosed orthopaedic or neurological disorder
• a history of lower limb surgery
• The presence of scoliosis
• Tightness in the gastrocnemius muscle
• Participants who did not consistently attend the intervention programme (i.e., those who missed two or more sessions out of the 12 sessions)

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Hamstring Muscle Tightness	4 weeks	Hamstring tightness will be assessed using the PostureScreen Mobile application, a validated tool for photographic posture and joint angle analysis. Participants will lie supine on a treatment table with the non-test leg stabilized using a strap. The test leg will be positioned with both the hip and knee at 90° flexion, adjusted with a stool and pillow as needed. The anatomical landmarks-the greater trochanter, lateral femoral condyle, and lateral malleolus-will be marked on the test leg. While the participant wears minimal clothing, a lateral photograph will be taken from 1.5 metres using a tripod-mounted smartphone. Participants will be instructed to extend their knee as much as possible with their ankle dorsiflexed. The application will calculate the knee extension angle from the marked points, and the range of motion will be recorded in degrees. The test will be repeated if compensatory movements are observed.
Hamstring Skinfold Thickness	4 weeks	The site will be marked at the midpoint of the posterior thigh, halfway between the ischial tuberosity and the popliteal region. The skinfold will be grasped 1 cm from the marked point using the thumb and index finger, maintaining consistent pressure throughout the measurement. Skinfold thickness will be measured with a skinfold calliper (Holtain Ltd, Crymych, UK). The reading will be taken 3-4 seconds after applying the calliper and then recorded. At least two measurements will be taken with a one-minute interval between them. Results will be recorded in millimetres (mm).

Secondary Outcome Measures

Name	Time	Method
Pain Threshold	4 weeks	A pressure algometer will be used to assess the sensitivity of the area where pain is felt and to obtain a quantitative measure of pressure perception. In the assessment, a digital algometer (Algometer Commander, Jtech Medical, 801-478, USA) will be used. For the measurement, the participant will be positioned in the prone position. The motor point on the participant's hamstring muscle will be marked with a pen. The calibrated algometer, with a probe tip of 1 cm² diameter, will be placed perpendicularly on the marked point of the hamstring muscle. The physiotherapist will gradually apply pressure, and pressure will be increased until the participant perceives pain. Upon the participant's signal indicating pain, the pressure will be stopped and the probe will be removed. This test will be repeated three times, and the average value will be recorded.
Functional Muscle Strength	4 weeks	The "Five Times Sit-to-Stand Test" will be used to assess functional muscle strength. This test will evaluate the functional strength of the lower extremity, transitional movements, balance, and risk of falling. Participants will be asked to sit on a chair with a straight back and a seat height of 43-45 cm from the ground. They will be instructed to cross their arms over their chest, placing their hands on the opposite shoulders, and to stand up and sit down five times as quickly as possible without pausing. The test will begin with the participant standing, feet shoulder-width apart, and the trunk upright. Each complete sit-to-stand movement will be counted as one repetition. The time taken to complete five repetitions will be measured with a stopwatch and recorded in seconds. The stopwatch will be stopped when the participant stands up for the fifth time, and the result will be documented.

Trial Locations

Locations (1)

Cyprus International University; 🇹🇷 Mersin, Lefkosa, Turkey