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临床试验/NCT01419301
NCT01419301已完成不适用

Mindfulness Based Stress Reduction in MS

Stony Brook University1 个研究点 分布在 1 个国家目标入组 31 人开始时间: 2011年5月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
31
试验地点
1
主要终点
Electronic measure of needle disposals (MEMS TrackCaps)

研究概览

简要总结

This study focuses on stress, cognition, mood and fatigue and its effect on medication compliance. Medication compliance is measured by the weight of discarded needles. The investigators will be administering neuropsychological testing at baseline and the final visit. The subjects will complete self-report assessments during their 8 weeks in the study.

Group A will have additional weekly phone support for meditation, while Group B will have meditation training only.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Single (Investigator)

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

  • •Patients with either definite MS according to the revised McDonald criteria (Polman 2005) or patients with CIS (defined as an initial MS relapse with objective documentation and 2 or more lesions within the CNS of which at least one must involve the brain)
  • •Patients on GA therapy for at least 6 months
  • •Age 18 - 70

排除标准

  • •Unwilling to comply with study procedures
  • •Use of other DMT in conjunction with GA
  • •Unable to provide informed consent.
  • •Current (past 30 days) substance abuse
  • •Newly initiated (past 30 days) psychiatry treatment
  • •Enrolled in another program of meditation in the past six months.

结局指标

主要结局

Electronic measure of needle disposals (MEMS TrackCaps)

时间窗: Medication adherence will be measured by total number of missed doses, calculated from total needle disposals. The total number of missed doses across the six weeks will be compared between the two treatment groups at study end.

During the six-week MSBR program, medication adherence will be monitored with a widely used electronic measure of needle disposals (MEMS TrackCaps) This method has been demonstrated to be more accurate in MS than data obtained from either self-report or interview. At one month intervals the patient will bring the needle container to the Study Coordinator. All patients who attend at least introduction session and one telephone session will be included in the analysis.

次要结局

  • Perceived Stress Scale-10(Baseline, 1 X between weeks 3-7, Week 8)
  • Chicago Multiscale Depression Inventory (CMDI)(Baseline, 1 X betweeen Weeks 3-7, Week 8)
  • State Trait Anxiety Inventory (STAI)(Baseline, 1 X betweeen Weeks 3-7, Week 8)
  • Holmes and Rahe Social Readjustment Rating Scale (SRRS(Baseline, 1 X between weeks 3-7, Week 8)
  • Positive and Negative Affect Scale (PANAS)(Baseline, 1 X between Weeks 3 - 7, Week 8)
  • Fatigue Severity Scale (FSS)(Baseline, 1 X between Weeks 3 - 7, Week 8)
  • Expanded Disability Status Scale (EDSS)(Baseline and Week 8)
  • Physiologic Markers of Stress(Baseline and Week 8)
  • Physiologic Maker of Stress(Baseline, 1 X between Week 3 - 7, Weeek 8)
  • MACFIMS neuropsychological battery(Baseline and Week 8)

研究者

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

Lauren Krupp

Professor

Stony Brook University

研究点 (1)

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