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临床试验/NCT03398408
NCT03398408已完成不适用

Cognitive Flexibility Training in Persistent Pain

Washington University School of Medicine1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2017年12月29日最近更新:
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
150
试验地点
1
主要终点
Does cognitive training over five weeks improve cognitive flexibility performance scores in chronic hip, knee, and back pain patients?

研究概览

简要总结

To determine whether participation in a cognitive training program over a training period of five weeks improves cognitive flexibility in patients with chronic hip, knee, and back pain.

详细描述

This project is a single-center prospective, randomized study to assess whether cognitive flexibility can be improved through training on a Lumosity®-based training module over the course a five week timeframe in patients with chronic hip, knee, and back pain; and whether changes in cognitive flexibility will correlate with perceived pain scores.

研究设计

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

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Adults age 18 to 70 with chronic hip, knee, or low back pain for >3 months
  • •Documented moderate to severe chronic pain
  • •English as a primary language
  • •Access to a computer at home and an email account

排除标准

  • •Diagnosed Alzheimer's or documented severe cognitive impairment
  • •Lack of email/lack of basic computer skills
  • •Has undergone an interventional pain procedure within one week prior to enrollment
  • •Are scheduled to undergo a pain procedure during the five weeks of complete cognitive training

研究组 & 干预措施

Intervention

Experimental

Patients in both groups will complete paper-pencil TMT A and B and the CWMST, the computer-based TMT A and B and Color Match, and NCPT tests upon enrollment into the study.

Participants in the intervention group will then be provided with the Lumosity cognitive flexibility training module and complete daily training for a total of five weeks. 1-3 days after completion of their training, all patients will be invited to complete the computerized versions of the TMT A and B, Color Match, and NCPT tests again on their personal computers.

干预措施: Training (Behavioral)

Control

No Intervention

Patients in both groups will complete paper-pencil TMT A and B and the CWMST, the computer-based TMT A and B and Color Match, and NCPT tests upon enrollment into the study.

Patients in the control group will complete all tests upon enrollment and approximately five weeks after their initial testing, but will not participate in training.

结局指标

主要结局

Does cognitive training over five weeks improve cognitive flexibility performance scores in chronic hip, knee, and back pain patients?

时间窗: Up to 5 months

The primary outcome, i.e. NCPT score, will be assessed before and after five weeks of cognitive training. T-test will be used to compare the change in NCPT score between the training and the control group.

次要结局

未报告次要终点

研究者

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

simon.haroutounian

Assistant Professor of Anesthesiology

Washington University School of Medicine

研究点 (1)

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