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临床试验/NCT01894282
NCT01894282已完成3 期

Mind Body Intervention for Chronic Lower Back Pain: A Pilot Study

Canandaigua VA Medical Center2 个研究点 分布在 1 个国家目标入组 4 人开始时间: 2013年7月1日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
4
试验地点
2
主要终点
Visual Analogue Scale

研究概览

简要总结

This pilot study will evaluate the feasibility of having a non-behavioral health provider deliver a combination of manual therapy (MT) and cognitive behavioral therapy for pain (CBT-p). In addition, we will evaluate differences in outcomes in patients undergoing the combined intervention of CBT-p and MT and those undergoing MT alone.

详细描述

Given that this is a pilot study we will use simple descriptive statistics for patient characteristics, including age, sex, BMI and baseline scores on outcome measures. In addition we will assess the inter-rater reliability of the scoring of the delivery of the CBT-p by the two trained practitioners utilizing kappa statistics. We will perform data analyses using SPSS.

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
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 69 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 18 to 69 years of age with CLBP who are
  • "high risk" for poor prognosis based on SBST
  • currently undergoing chiropractic care.

排除标准

  • Contraindications to either MT or CBT-p.
  • Patients who are currently undergoing CBT-p
  • who have been treated for substance abuse in the past year.

结局指标

主要结局

Visual Analogue Scale

时间窗: Baseline and 6 weeks post baseline (immediately post intervention)

The VAS is a patient completed analogue measure that evaluates pain intensity on a 100 mm long horizontal line, which is anchored at each end with a statement representing the extremes of the dimension being measured. In this case the left hand side reads, "no pain" and the right hand side reads "worst pain possible". The VAS scale utilized will assess pain at the current time. The VAS has been established as a reliable, valid and generalizable measure that can be administered in a wide range of clinical and experimental settings.

次要结局

  • PROMIS Global Health Scale (GHS)(Baseline and 6 weeks post baseline (immediately post intervention))

研究者

发起方
Canandaigua VA Medical Center
申办方类型
Fed
责任方
Principal Investigator
主要研究者

Paul Dougherty, DC

Chiropractor

Canandaigua VA Medical Center

研究点 (2)

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