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临床试验/NCT03335618
NCT03335618已完成不适用

A First-in-Kind Randomized, Controlled Pilot Clinical Trial Testing Proactive vs Reactive Management of a Symptom Triad in Multiple Sclerosis

University of California, San Francisco1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2017年10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
30
试验地点
1
主要终点
Feasibility of an active symptom monitoring and intervention protocol

研究概览

简要总结

The purpose of this 12-week, exploratory pilot clinical trial is to continuously and remotely assess a triad of bothersome multiple sclerosis (MS) symptoms (BAM: bladder, ambulation, mood) and test the benefit of proactively treating these symptoms according to an evidence-based, multi-disciplinary, personalized protocol.

详细描述

MS is a chronic, debilitating disease of the central nervous system affecting approximately 2 million people worldwide and more than 400,000 individuals in the US. MS is the most common cause of non-traumatic neurological disability in young adults. Symptoms typically first afflict individuals during the prime of their professional and reproductive lives, between the ages of 20 and 40. Many affected individuals are unemployed, physically disabled, and at high risk for social isolation. While disease-modifying therapies (DMTs) can significantly reduce accumulation of disability in MS, patients still experience symptoms across a range of functional domains. Symptoms can include problems with bladder, walking, and mood (depression and anxiety). Often, these symptoms are only partially evaluated during routine MS clinic visits, and the long interval between clinic visits can result in them not being optimally managed.

The goal of the current study is to pilot a system of proactively monitoring a combination of symptoms (bladder, ambulation and mood) using an activity monitor and a smartphone.

Adult patients with MS who are experiencing symptoms in at least 2 of the 3 domains (bladder, ambulation, mood) will be enrolled. Visits will be at baseline (can be same day as routine visit to the MS clinic), and 3 months. Short surveys (<3 minutes to complete) will occur weekly, and longer surveys will occur at baseline, 6 weeks and 3 months. FitBit activity monitors will be worn for the entire 3 months.

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
Double (Participant, Care Provider)

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

  • •Any individual above the age of 18 with a confirmed diagnosis of MS
  • •Access to a smartphone
  • •Access to Wi-Fi at home
  • •Able to walk (including with a cane or walker)
  • •Willing to fill out surveys at multiple time points

排除标准

  • •Clinician's assessment of cognitive, dexterity, or visual impairment limiting ability to use a smartphone and subsequent technologies required by the study
  • •Inability to walk

研究组 & 干预措施

Active Coaching and Monitoring

Experimental

干预措施: Activity Monitoring and Symptom Coaching (Other)

Passive Monitoring

Sham Comparator

干预措施: Passive Activity Monitoring (Other)

结局指标

主要结局

Feasibility of an active symptom monitoring and intervention protocol

时间窗: 12 weeks

To evaluate feasibility of the intervention, we will calculate how many patients remain in the study, levels of patient satisfaction with the monitoring and intervention, and we will analyze patient and provider feedback.

次要结局

  • Improvement in bladder symptoms in MS participants.(12 weeks)
  • Improvement in mood symptoms in MS participants.(12 weeks)
  • Improvement in ambulation symptoms in MS participants(12 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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