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临床试验/NCT04571034
NCT04571034已完成不适用

Effects of Roller Massage on Short-Term Passive Muscle Stiffness

Jeffrey Sykora2 个研究点 分布在 1 个国家目标入组 48 人开始时间: 2021年2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
48
试验地点
2
主要终点
Change in Quadriceps Stiffness

研究概览

简要总结

Muscle stiffness is associated with a variety of variables that affect health, however there is limited research on the effect of massage on muscle stiffness, and existing research does not quantify the intensity of massage. Thus trial will determine the effect of roller massage on quadriceps muscle stiffness and passive range of motion.

详细描述

Following screening for eligibility and consent, subjects will be assigned randomly to one of three groups: a placebo control group and two roller massage groups (treatment groups). The treatment groups will each receive a single bout of roller massage. One treatment group will receive a massage at medium intensity (25 newtons of force directed perpendicular to surface of thigh), the other treatment group at high intensity (45 newtons of force directed perpendicular to surface of thigh). The placebo group will receive a single bout of sham ultrasound. Both placebo and treatments will be delivered to the anterior thigh with the participant in a supine position. Each procedure will last for 10 minutes. In all groups, muscle stiffness, natural oscillation frequency, elasticity, relaxation time, and creep at the vastus lateralis will be measured using a myotonometer. PROM for knee flexion will also be measured in both groups using goniometry. All measurements will be taken at 3 different times: immediately before treatment or placebo, immediately after treatment or placebo, and 30 minutes after treatment or placebo. Myotonometric measurements of the vastus lateralis will be taken 2/3 of the way down between the anterior superior iliac spine and lateral aspect of the patella, in accordance with guidelines for the Surface ElectroMyoGraphy for the Non-Invasive Assessment of Muscles. For goniometric measurement, participants will be in supine position on an examination table. The investigator will flex the participant's hip to 90 degrees and then, using a dynamometer (to ensure consistent applied force for all participants), flex the participant's knee. To measure knee flexion PROM, the goniometer will be positioned with the axis at the lateral epicondyle of the femur, the stationary arm in line with the lateral midline of the femur toward the greater trochanter, and the moving arm in line with the fibular head and lateral malleolus. During the time between the second and third measurements, subjects will be asked to sit quietly.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 30 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • Prior history of significant vascular or neuromuscular illness or impairment affecting the lower limbs
  • Serious injuries to the back or legs in the last six months
  • Discomfort or pain in the back or legs
  • Use of pain and anti-inflammatory medications
  • Any contraindications to massage treatment or ultrasound
  • Body mass index (BMI) >30 kg/m2.

结局指标

主要结局

Change in Quadriceps Stiffness

时间窗: 1 hour (at baseline, immediately after treatment and 30 minutes later)

Quadriceps stiffness will be measured using a myotonometer at baseline, immediately after treatment, and 30 minutes later.

Change in Passive Range of Motion

时间窗: 1 hour (at baseline, immediately after treatment and 30 minutes later)

Range of motion of the knee will be measured using a goniometer at baseline, immediately after treatment, and 30 minutes later.

次要结局

  • Change in Quadriceps Natural Oscillation Frequency(1 hour (at baseline, immediately after treatment and 30 minutes later))
  • Change in Quadriceps Creep(1 hour (at baseline, immediately after treatment and 30 minutes later))
  • Change in Quadriceps Elasticity(1 hour (at baseline, immediately after treatment and 30 minutes later))
  • Change in Quadriceps Relaxation Time(1 hour (at baseline, immediately after treatment and 30 minutes later))

研究者

发起方
Jeffrey Sykora
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Jeffrey Sykora

Study Coordinator

University of Kentucky

研究点 (2)

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