跳至主要内容
临床试验/NCT07274540
NCT07274540已完成不适用

The Effects Of Front Arm Band Orthosis On Pain, Functionalite And Grip Force Evaluation To Person Of Play Instrument

Medipol University2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2020年1月16日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
30
试验地点
2
主要终点
Change from Baseline in Pain Intensity as Measured by the Visual Analog Scale (VAS)

研究概览

简要总结

This interventional clinical study investigates the effectiveness of applying a forearm strap orthosis in 30 individuals experiencing forearm pain due to playing a musical instrument. Participants used the orthosis for 4 weeks. The primary objective is to evaluate the changes in pain levels and grip strength following this period. The study also explores the potential of this intervention to improve functionality and quality of life.

详细描述

The therapeutic and biomechanical effects of orthoses are utilized in the management of musculoskeletal disorders frequently encountered in instrumental musicians; this interventional study aims to prospectively evaluate the effect of a standardized forearm strap orthosis intervention on pain intensity, grip strength, and upper extremity functionality after a 4-week usage period in instrumental musicians. The study employs an Interventional type, single-group assignment, non-randomized pre-post design, enrolling 30 individuals from the Sulukule Art Academy of Fatih Municipality who meet the inclusion criteria. The primary outcome measures are the McGill Melzack Pain Questionnaire and Visual Analogue Scale (VAS) scores, grip strength values measured with the Jamar dynamometer, and Disabilities of the Arm, Shoulder, and Hand (DASH-T) Questionnaire scores, all obtained pre- and post- orthosis use. The secondary outcome measure is the evaluation of quality of life using the Short Form 36 (SF-36) Quality of Life Survey.

研究设计

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

入排标准

年龄范围
18 Years 至 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Participants were between 18 and 55 years old at the time of enrollment.
  • Participants had been playing an instrument for more than six months.
  • Participants had been playing an instrument for at least one hour a day.
  • Participants were willing and able to adapt to orthotic treatment.

排除标准

  • Participants had a history of surgery and/or trauma to the elbow where orthosis treatment was required.
  • Participants were receiving physiotherapy treatment within the last 6 months.
  • Participants had an acute injury that prevented performance.

结局指标

主要结局

Change from Baseline in Pain Intensity as Measured by the Visual Analog Scale (VAS)

时间窗: Baseline and 4 weeks

The VAS was a valid measure that recorded participants' perceived pain intensity. A decrease in the VAS score was evaluated. VAS ranges from a minimum of 0 (no pain) to a maximum of 10 (the most severe pain imaginable); higher scores indicate worse (more severe) pain.

Change from Baseline in Pain Intensity as Measured by the Visual Analog Scale (VAS)

时间窗: Baseline and 4 weeks

The VAS was a valid measure that recorded participants' perceived pain intensity. A decrease in the VAS score was evaluated. VAS ranges from a minimum of 0 (no pain) to a maximum of 10 (the most severe pain imaginable); higher scores indicate worse (more severe) pain.

Change from Baseline in Pain Experience Measured by the McGill Melzack Pain Questionnaire Score (MPQ-PRI)

时间窗: Baseline and 4 weeks

It was a questionnaire that measured the sensory, emotional, and evaluative aspects of pain. The decrease in the score was evaluated. The MPQ-PRI ranges from a minimum of 0 (no pain) to a maximum of 78 (the most severe and comprehensive pain); higher scores indicate a worse and more multidimensional pain experience.

Change from Baseline in Isometric Grip Strength using Jamar Dynamometer

时间窗: Baseline and 4 weeks

The maximum isometric grip strength of the affected hand was measured using the Jamar Dynamometer device.

Change from Baseline in Upper Extremity Functional Status using the Disabilities of the Arm, Shoulder, and Hand (DASH-T) Score

时间窗: Baseline and 4 weeks

It was a standardized questionnaire that measured upper extremity disability and its symptoms. A decrease in the DASH-T score (increased functionality) was evaluated.

次要结局

  • Change from Baseline in Quality of Life (SF-36)(Baseline and 4 weeks)

研究者

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

Tuba YILDIZ

Lecturer

Medipol University

研究点 (2)

Loading locations...

相似试验

Use Of Orthotics To Reduce Pain In Musicians | 临床试验