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临床试验/NCT02146482
NCT02146482已完成不适用

Evaluating Change in Back Pain From Access to a Sit-stand Workstation

Stanford University2 个研究点 分布在 1 个国家目标入组 57 人开始时间: 2013年4月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
57
试验地点
2
主要终点
Change in Back Pain

研究概览

简要总结

The purpose of the study is to evaluate the changes in back pain from access to a sit-stand workstation. Other muscle and joint pain and/or discomfort will also be evaluated. We hypothesize that access to a sit-stand workstation will allow one to experience postural variation and reduce back pain.

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
None

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

  • Back pain lasting ≥3 months and reported at a minimum of 4 out of 10 on the pain scale.
  • Sits >6 hours out of an 8-hour work day for work purposes
  • Able and willing to fill out a daily survey for the first week prior to randomization
  • Participants must be >18 years of age. There are no gender/race-ethnic restrictions.
  • Ability to understand and the willingness to sign a written informed consent document.

排除标准

  • Unable to stand for at least 10 minutes.
  • Currently using a sit-stand desk

研究组 & 干预措施

Control

No Intervention

Did not receive an intervention during the active portion of the study (i.e. 12 weeks). After the active portion of the study, this group was given a sit-stand computer workstation.

Sit-stand computer workstation

Experimental

Given a sit-stand computer workstation to use at their place of work

干预措施: Sit-stand computer workstation (Other)

结局指标

主要结局

Change in Back Pain

时间窗: Baseline (Week 1) and Follow-Up (Week 18)

The Roland-Morris Disability Questionnaire is designed to assess self-rated physical disability caused by low back pain. The patient is asked to agree or disagree with 24 different statements related to their back pain. The end score is the sum of the agreed statements. The score ranges from 0 (no disability) to 24 (maximum disability).

次要结局

  • Change in Pain in Other Body Parts(At the conclusion of each work day for 12 weeks and 8 weeks later)

研究者

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

Kathleen Horst

Assistant Professor

Stanford University

研究点 (2)

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