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临床试验/NCT03827928
NCT03827928已完成不适用

The Acceptability, Feasibility, and Impact of a Group-based Yoga and Psychoeducation Program for Community-dwelling Adults With Multiple Sclerosis: A Randomized, Cross-over Pilot Study

Dartmouth-Hitchcock Medical Center1 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2019年7月1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
15
试验地点
1
主要终点
Feasibility of conducting a yoga intervention study

研究概览

简要总结

The purpose of the study is to assess the feasibility of a 6-week yoga and meditation intervention for people with multiple sclerosis (MS). The study will evaluate the impact of the program on fatigue, anxiety, depression, positive affect, and other measures. A sub-study will collect brain images using MRI on 2 subjects before and after the intervention to identify potential biological markers of MS related-fatigue.

详细描述

This study will recruit 20 subjects with multiple sclerosis (MS) to participate in a 6-week yoga/meditation program. Subjects will be randomly assigned to one of two groups. The first group will complete the yoga/meditation classes, followed by a waiting period. The second group will go through a waiting period, followed by yoga/meditation classes. Two subjects assigned to classes during the first session will be selected to participate in an MRI sub-study to look for biomarkers of MS-associated fatigue. All subjects will complete questionnaires and assessments during 3 clinic visits - at baseline, in between the class sessions, and at the end of the study. Questionnaires will also be mailed to subjects 6 weeks after the last study visit.

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
否

入选标准

  • •Diagnosis of Multiple Sclerosis with EDSS score equal to or less than 6 (within last year)
  • •18 years of age or older
  • •Ability to ambulate without assistance from a device or person
  • •Subjects taking medications for depression, fatigue, or anxiety must be stable for 8 weeks prior to baseline
  • •Able to read, write, and speak English
  • •Willing to refrain from participating in yoga or meditation outside of the study for the duration of enrollment
  • •Willing and able to give informed consent

排除标准

  • •Participation in yoga and/or meditation more than twice within 8 weeks prior to baseline.
  • •MS symptom exacerbation in the 8 weeks before baseline or other serious medical conditions that would impair ability to participate in the study.
  • •Any other reason that, in the investigator's opinion, would exclude the subject from participation in the study.
  • •Contraindication to scanning, including but not limited to ferromagnetic metal in the body, claustrophobia, inability to lie still or otherwise tolerate being in the scanner.
  • •Pregnant women must be excluded from the imaging component of the study due to unknown but possible risk of fetal exposure to the scanner. Women of child-bearing potential will take a confidential pregnancy test immediately prior to each scan session.

研究组 & 干预措施

Yoga/meditation

Experimental

A 6-week yoga/meditation intervention.

干预措施: Yoga/meditation (Behavioral)

Wait list

No Intervention

A wait list control period.

结局指标

主要结局

Feasibility of conducting a yoga intervention study

时间窗: At the clinic visit immediately following the yoga class session

The feasibility will be determined by the completion rates of the intervention. If fewer than 50% of subjects complete the intervention, it will be deemed unfeasible in the current format.

次要结局

  • Change in subject self-rated sleep disturbance(Through study completion, approximately 22 weeks)
  • Change in subject self-rated fatigue(Through study completion, approximately 22 weeks)
  • Change in subject self-rated anxiety(Through study completion, approximately 22 weeks)
  • Change in subject self-rated depression(Through study completion, approximately 22 weeks)
  • Change in subject self-rated pain interference(Through study completion, approximately 22 weeks)
  • Change in subject self-rated cognitive function(Through study completion, approximately 22 weeks)
  • Change in subject self-rated positive affect(Through study completion, approximately 22 weeks)
  • Change in subject self-rated quality of life(Through study completion, approximately 22 weeks)
  • Change in subject self-rated self-efficacy(Through study completion, approximately 22 weeks)
  • Change in subject cognition/processing speed(Through study completion, approximately 22 weeks)
  • Satisfaction rating of 6-week yoga program on a scale of 1 - 10(At the clinic visit immediately following the yoga/meditation class session)

研究者

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

Andrew D. Smith III

Principal Investigator

Dartmouth-Hitchcock Medical Center

研究点 (1)

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