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NCT Number: NCT06610058

Effects of Instrument Assisted Soft Tissue Mobilization Regarding Range of Motion and Lower Extremity Power

The goal of this clinical trial is to study the effects of instrument assisted soft tissue mobilization (IASTM) in healthy adult volunteers. The main questions it aims to answer are:

* Does IASTM treatment have an effect on range of motion (ROM) as measured in the hip, knee and ankle? * Does IASTM treatment have an effect on lower extremity power? Researchers will compare pre-test and post-test IASTM treatment intervention data to the pre-test and post-test data of the no treatment control intervention to see if IASTM works to change range of motion and/or lower extremity power.

Participants will:

* Complete a questionnaire on medical history and injury background * Have hip, knee and ankle range of motion (ROM) measurements taken on both lower extremities using a goniometer * Complete three trials of vertical jump testing using a Fleage Floor standing vertical jump measurement tester with one warm up first * Complete three trials of horizontal jump testing using a Woanger 12'x2.5' long jump mat and verified by a secondary measure using a tape measure with one warm up first * Be randomly assigned to either IASTM first treatment group or the wait/control first group * Receive IASTM treatment techniques including application of emollient to the skin to reduce friction on the surface followed by scanning the hamstrings, quadriceps, gastroc/soleus complex, and Achilles tendon using the HG8-Scanner tool for 15 strokes in each direction. Then the concave tool corresponding to the size of the structure being treated will be used (HG6-Large Multi-Curve, HG5-Medium Multi-Curve, HG4-Small Multi-Curve) for 15 strokes in each direction. * Simply wait for 20 minutes (the duration of time treatment with IASTM would require) when completing the control treatment. * Complete hip, knee and ankle range of motion and vertical and horizontal jump measure testing at the end of the first session. * Return within fourteen days after the first session in order to undergo the opposite experience (IASTM first means wait/control second and vice versa). * Undergo the same baseline pre-test measurements for range of motion and vertical and horizontal jump measure testing as the first session. * Experience the opposite treatment for the same time period as the first session. * Undergo the post-test range of motion and vertical and horizontal jump measure testing at the end of the second session for data comparison.

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Minot State University

Minot, North Dakota, 58707, United States

About this study

No further information to note than what is described in the summary or elsewhere

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Individuals from a small regional university student body, faculty and staff may choose to volunteer to participate in this study.

Exclusion criteria

  • Acute spinal cord injury with neurological deficits
  • Neurological disorders
  • Acute lower extremity injury such as sprain or strain
  • Acute lower extremity pain causing gait deviation
  • Any type of lower extremity fracture within the past 12 months
  • Lumbar disc pathology with radicular symptoms
  • Use of blood thinning or clotting medications
  • Known connective tissue disorder

Treatment and study plan

Instrument Assisted Soft Tissue Mobilization first Control second

Other

Instrument assisted soft tissue mobilization was utilized first on day one and wait-control was completed on second day.

Control first Instrument Assisted Soft Tissue Mobilization second

Other

This intervention involved waiting for 20 minutes between pre-test and post-test on day one and having Instrument Assisted Soft Tissue Mobilization on day two.

Primary outcomes

  1. Range of Motion

    Time frame: From baseline to end of session at one hour

    Bilateral hip flexion, extension and abduction, knee flexion and extension, ankle plantarflexion, dorsiflexion, inversion and eversion range of motion measurements were taken in supine or prone (whichever was appropriate) using a goniometer.

  2. Lower Extremity Power Horizontal Jump

    Time frame: From baseline to end of session at one hour

    Lower extremity power was measured by completing three trials of horizontal jump testing using a Woanger 12'x2.5' long jump mat with the distance verified by a secondary measure using a tape measure with one warm up first and 90 seconds to recover between each jump.

  3. Lower Extremity Power Vertical Jump

    Time frame: From baseline to end of session at one hour

    Lower extremity power was measured by completing three trials of vertical jump testing using a Fleage Floor standing vertical jump measurement tester with one warm up first and 90 seconds to recover between each jump.

Sponsors and collaborators

Lead sponsor

Beth Marschner

Other

Collaborators

  • Minot State University

Registry information

Official study title

Effects of Instrument Assisted Soft Tissue Mobilization on Healthy Tissue Regarding Range of Motion and Lower Extremity Power

Acronym: (IASTM)

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Sep 24, 2024
Registry last updated
Sep 24, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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