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临床试验/NCT06612983
NCT06612983已完成不适用

Effects of Instrument Assisted Soft Tissue Mobilization on Healthy Tissue Regarding Range of Motion and Gait

Beth Marschner2 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2023年1月9日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
70
试验地点
2
主要终点
Range of Motion

研究概览

简要总结

The goal of this clinical trial is to study the effects of instrument assisted soft tissue mobilization (IASTM) in healthy tissue of 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 ankle and knee?
  • Does IASTM treatment have an effect on movement patterns including gait - how a person walks? Researchers will compare pre-test and post-test data from the same individual on their day with treatment to the pre-test and post-test data from the same individual on their day without treatment to see if ROM or gait are effected by use of IASTM.

Participants will:

  • Complete a past medical and injury history questionnaire
  • Have ankle and knee range of motion (ROM) measurements taken on both lower extremities using a goniometer
  • Undergo a gait analysis to determine center of gravity, center of pressure, step length, stride length, and stride frequency using Noraxon MyoMuscle Ultium Insoles
  • Undergo IASTM treatment techniques using the HawkGrips tools including applying emollient to the skin to reduce friction on the surface followed by scanning the gastroc/soleus complexes and Achilles tendons using the HG8-Scanner tool for 15 strokes in each direction to identify areas of concern, 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. Treatment techniques should last for 10 minutes in total on each side.
  • Complete the ankle and knee ROM measurements as well as gait analysis again to document progress at the end of the first session.
  • Return three to seven days after the first session in which the subject will have the walking treatment.
  • Undergo the same baseline pre-test measurements for range of motion and gait analysis as the first session
  • Experience the walking treatment by walking for the same time period that the IASTM treatment took at the first session
  • Undergo the post-test range of motion and gait analysis for data comparison.

详细描述

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

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

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

排除标准

  • 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

结局指标

主要结局

Range of Motion

时间窗: From baseline to end of session at one hour

Bilateral knee flexion and extension as well as ankle plantarflexion, dorsiflexion, inversion and eversion range of motion measurements were taken in supine using a goniometer.

Gait

时间窗: From baseline to end of session at one hour

Gait analysis was conducted using Noraxon MyoMuscle System with Ultium insoles placed in the participants shoes. The software collected data on center of gravity, center of pressure, step length, stride length, and stride frequency.

次要结局

未报告次要终点

研究者

发起方
Beth Marschner
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Beth Marschner

Assistant Professor

Minot State University

研究点 (2)

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