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临床试验/NCT04531306
NCT04531306已完成不适用

An Analysis of Kinesio® Tape on Myofascial Pain Syndrome of the Iliotibial Band

North Dakota State University2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2020年10月4日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
50
试验地点
2
主要终点
with-in subject differences pre- and 48-hour post- tape application

研究概览

简要总结

Participants will report for two research sessions. Prior to arrival, membership to a club sports team will be confirmed via email. The first session will require one hour, while the second will require 30 minutes. Maximum amount of time expected is one and a half hours, over two sessions in 48 hours. The 1st and 2nd sessions will be separated by 48 hours. Upon arrival for session 1, informed consent will be obtained along with the following demographic information: age, sex, height, weight, dominant leg, and sport. Next, the participant will complete the Musculoskeletal Questionnaire (MQ) in regard to the last 12 months. Participants will then be assessed for trigger points in their dominant side iliotibial band via palpation. Diagnostic criteria for trigger point will be modeled after Travell and Simons: taut band, pain upon palpation, referred pain, and a local twitch response. Up to four trigger points will be marked on the subject's skin with marker or pen. Pain pressure threshold will be obtained via algometer, using the terminology "Tell me the first moment you experience pain by verbalizing 'pain' ". Then, three pain pressure threshold readings will be taken per trigger point and then averaged by the researcher. Kinesiology tape will then be applied to the identified trigger points using the Fascial Technique. Pain pressure threshold will be obtained again with the same protocols 10 minutes after the tape is applied. The participant will be asked to wear the tape for 48 hours. Upon arrival for session 2, the application of the tape will be confirmed. With the participant's choice to continue in the study, a third and fourth measurement of pain pressure threshold will be obtained: one with the tape remaining on, and another 10 minutes after removal of the tape. Again, three pain pressure threshold readings will be taken per trigger point and then averaged by the researcher.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Factorial
主要目的
Treatment
盲法
None

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

  • member of club sports team

排除标准

  • acute quadriceps strain in last six months
  • knee surgery in last six months
  • acute hamstring strain in last six months
  • allergy to adhesive
  • malignancies
  • cellulitis
  • skin infection
  • fragile skin

结局指标

主要结局

with-in subject differences pre- and 48-hour post- tape application

时间窗: 48 hours

measured by pain pressure threshold (N/s2) via algometer

with-in subject differences pre- and 10-minute post- tape application

时间窗: 10 minutes

measured by pain pressure threshold (N/s2) via algometer

with-in subject differences 10-minute post- and 48-hour post- tape application

时间窗: 48 hours

measured by pain pressure threshold (N/s2) via algometer

with-in subject differences 48-hour post- tape application and post- 10- minute tape removal

时间窗: 10 minutes

measured by pain pressure threshold (N/s2) via algometer

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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