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临床试验/NCT05373056
NCT05373056Unknown不适用

Effects of Scapular Strength Exercise for Patients With Lateral Epicondylalgia a Randomized Clinical Trial

University of Alcala2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2022年2月28日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
60
试验地点
2
主要终点
Visual Analog Scale for Pain

研究概览

简要总结

the aim of the study is to determine whether a scapular strength exercise program combined with a conventional exercise program in epicondylar region in patients with lateral epicondylalgia produces statistically significant improvements in pain in the short and medium term compared to a conventional exercise program.

详细描述

It is a single-blind clinical trial design, with third-party evaluation. There are two groups, the control group and the experimental group. In the control group, only the conventional exercise program for epicondylar muscles will be performed and the experimental group will also perform a scapular exercise program. Group assignment is randomized using the G* POWER software program, following the inclusion and exclusion criteria. Variables related to pain, functionality, pressure pain threshold, prehensile strength and quality of life will be measured. The study will last 7 months.

研究设计

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

入排标准

年龄范围
30 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • tenderness over the epicondyle.
  • Clinical diagnosis of LD for at least 3 months.
  • Positive Mills and Maudsley test

排除标准

  • Patients with carpal tunnel syndrome, rheumatoid arthritis, cervical root syndrome, rotator cuff tendinopathy.
  • Fractures or surgical history in the shoulder or elbow.
  • History of elbow immobilization.
  • Limitation in range of motion of the shoulder.
  • Having undergone upper limb surgery in the last 6 months
  • Unhealed wound in the region in the treatment area
  • Impairment at a cognitive level that makes understanding with the therapist impossible.
  • Neural entrapment of the radial nerve.
  • Corticosteroid infiltration in the upper limb to be treated.

结局指标

主要结局

Visual Analog Scale for Pain

时间窗: 4 weeks

It will be measured with a 10 cm long horizontal line with descriptors at each end to help subjects identify their level of pain. The participants will mark with a cross the point of the line that most corresponds to the intensity of their symptoms. When interpreting the VAS, the respondent's cross position is usually assigned a score between 0 and 10. If documented on paper, pressures can simply be transferred to a scale of 100 values using a millimeter tape measure, although division into hundredths is considered sensitive enough.

次要结局

  • Functionality(4 weeks)
  • grip strength(4 weeks)
  • pressure threshold(4 weeks)
  • The Quality of the lifestyle(4 weeks)

研究者

发起方
University of Alcala
申办方类型
Other
责任方
Principal Investigator
主要研究者

Alejandro Ayuso Pablo

Principal investigator

University of Alcala

研究点 (2)

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