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临床试验/NCT04351477
NCT04351477Unknown不适用

The Effect of Mechanical Massage Chair on Musculoskeletal Pain Improvement for Endoscopists and Endoscopy Nurses

Seoul National University Hospital1 个研究点 分布在 1 个国家目标入组 25 人开始时间: 2020年6月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
25
试验地点
1
主要终点
Visual analogue scale

研究概览

简要总结

The effect of mechanical massage chair on musculoskeletal pain improvement for endoscopists and endoscopy nurses

详细描述

Randomized, open-label, cross-over study

  1. 1st phase Massage chair group (20 minutes/session, 3 sessions/week, 3 weeks), vs. control (no use of massage chair)
  2. Wash-out period (9 weeks)
  3. 2nd phase (cross-over) Massage chair group (20 minutes/session, 3 sessions/week, 3 weeks), vs. control (no use of massage chair)
  • Msculoskeletal pain questionnaires (VAS, NDI, SPADI)
  1. 1st phase: at baseline, 1.5 wk, 3 wk 2) 2nd phase: at baseline, 1.5 wk, 3 wk, 9wk after the end of treatment

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Other
盲法
None

盲法说明

  1. Randomization by allocation concealment
  2. Open label, cross-over design

入排标准

年龄范围
20 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Endoscopists or endoscopic nurses working at Seoul National University Hospital Gangnam Center

排除标准

  • •Spine disease, skin disease, acute inflammation, electrical heart device, thromboembolism, fracture, osteoporosis, varicose vein
  • •Pregnancy

研究组 & 干预措施

Massage chair group

Experimental

Use mechanical massage chair for 20 minutes/1 session, 3 sessions/week, for 3 weeks

干预措施: Massage chair (Device)

Control

No Intervention

No use of mechanical massage chair for 3 weeks

结局指标

主要结局

Visual analogue scale

时间窗: The change of VAS value at baseline, 1.5 week, 3 weeks during treatment, and 9 weeks after treatment

range: 0-10 (0: no pain; 10: worst possible pain)

次要结局

  • Neck disability index (NDI)(The change at baseline, 1.5 week, 3 weeks during treatment, and 9 weeks after treatment)
  • Shoulder pain and disability index (SPADI)(The change at baseline, 1.5 week, 3 weeks during treatment, and 9 weeks after treatment)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Su Jin Chung

Professor

Seoul National University Hospital

研究点 (1)

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