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临床试验/NCT07316946
NCT07316946尚未招募不适用

Effects of Neuromuscular Taping on Shoulder Pain and Function in Pitchers: A Clinical Trial

Sandra Jiménez-del-Barrio1 个研究点 分布在 1 个国家目标入组 62 人开始时间: 2026年2月13日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
62
试验地点
1
主要终点
Actual Pain Intensity

研究概览

简要总结

Effects of Neuromuscular Taping on Shoulder Pain and Function in Pitchers: A Clinical Trial

详细描述

Randomized clinical trial 2 arms

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Double (Participant, Outcomes Assessor)

盲法说明

participants and outcome assessors will be blinded

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

  • age over 18 years
  • compete in a sport that involves overhead movement patterns
  • train at least 2 hours per week
  • shoulder pain lasting more than six weeks
  • shoulder pain related to sports activity
  • understand Spanish fluently enough to complete the questionnaire assessment.

排除标准

  • presence of red flags that could suggest fractures, dislocations, or complete tendon ruptures, among others
  • neurological pathologies
  • other severe pathologies such as inflammatory arthritis, frozen shoulder
  • having received corticosteroid injections or physiotherapy treatment in the last six months
  • presence of previous surgeries
  • pregnancy
  • cognitive deficits that could limit the comprehension of the questionnaires or the physical evaluation
  • skin problems that would be a contraindication for any type of bandage.

结局指标

主要结局

Actual Pain Intensity

时间窗: Baseline, after 30 minutes of the intervention and 72 hours after intervencion

Pain intensity will be assessed using a 10-cm visual analog scale (VAS), ranging from 0 (no pain) to 10 (worst imaginable pain). Participants will be asked to rate the intensity of pain experienced at the time of measurement

Pain Intensity during the arm elevation

时间窗: Baseline, 30 minutes after intervention and 72 hours after intervention

Pain intensity will be assessed using a 10-cm visual analog scale (VAS), ranging from 0 (no pain) to 10 (worst imaginable pain). Participants will be asked to rate the intensity of pain experienced during arm elevation.

次要结局

  • Static Scapular Position(Baseline, 30 minutes after intervention and 72 hours after intervention)
  • Range of Motion(Baseline, 30 minutes after intervention and 72 hours after intervention)
  • Functional Capacity(Baseline, 30 minutes after intervention and 72 hours after intervention)

研究者

发起方
Sandra Jiménez-del-Barrio
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Sandra Jiménez-del-Barrio

PhD Physiotherapist

University of Valladolid

研究点 (1)

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