ACTRN12616001722482已完成未知
An investigator initiated validation study comparing ViMove with standardized outcome measures of function and disability in adults with chronic low back pain.
Precision Brain, Spine and Pain Centre0 个研究点目标入组 40 人开始时间: 2016年12月15日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 40
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 Years 至 65 Years（—）
- 性别
- All
入选标准
- •1.Adults aged over 18 and < 65
- •2.Low Back pain for > 3 months
- •3.Pain score (as measured by a Numeric Rating Scale [NRS]) at baseline = or > 3
- •4.Able to provide informed consent
- •5. Does not meet any of the exclusion criteria
排除标准
- •1.Acute back pain (< 3 months)
- •2.Performance of assessment protocol is contraindicated for the participant
- •3.Illness or injury other than lower back pain that impacts upon function or causes disability or an inability to move independently.
- •4.Is pregnant or planning to become pregnant during the course of the study
- •5.Participants with a severe hearing impairment or inability to follow verbal instructions.
- •6.Significant medical or psychological abnormalities/conditions, a history of substance abuse or recent history of a medical-surgical intervention that in the opinion of the investigator would interfere either with the ability to complete the study or the assessments.
- •7.Known allergy skin reaction to tapes and plasters.
- •8.Participant who is currently enrolled in an investigational drug or device study
- •9.Inability to comply with study requirements or complete questionnaires in English independently.
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