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临床试验/NCT03969537
NCT03969537已完成不适用

Telemedicine Follow-up for Patients With Cervical Dystonia Treated With Neurotoxin Injections

Vanderbilt University Medical Center1 个研究点 分布在 1 个国家目标入组 27 人开始时间: 2019年4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
27
试验地点
1
主要终点
Patient Satisfaction with Telehealth

研究概览

简要总结

Many cervical dystonia (CD) patients are limited in their ability to travel to the clinic for follow-up in between injection visits.

A telemedicine visit at the time of peak effectiveness of neurotoxin treatment may be valuable in informing the neurologist's choice of muscle selection and/or dose for the next injection visit. The primary objective of this study is to investigate both patient and physician satisfaction with the use of our telemedicine tool for this type of follow-up. After assessment of the subject, the neurologist will decide whether or not the telemedicine visit was informative to the upcoming injection visit. Subjects will answer questions at the end of the visit regarding their satisfaction with the follow-up and overall telemedicine communication. The principle investigator will complete a similar survey with additional questions about information gathered from the visit to assess the primary objective.

A secure video communications platform will be used for the visit, which will occur 2-4 weeks after the patient's last neurotoxin injection (around the time of peak effectiveness). The investigating neurologist will remotely assess the patient and make notes for the next injection visit.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • Male or female subjects of any race, aged 18 and above
  • Diagnosed with cervical dystonia and being treated with neurotoxin injections at Vanderbilt University Medical Center
  • The subject, or if appropriate their medical decision maker, is willing and able to provide written informed consent.
  • Email and internet access
  • Personal computing device with audio/video capability

排除标准

  • Subjects for whom participation in the study may cause medical harm

结局指标

主要结局

Patient Satisfaction with Telehealth

时间窗: 4 months

This questionnaire measures patient satisfaction with the telehealth visit scored 7 to 27

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

David Charles

Professor of Neurology

Vanderbilt University Medical Center

研究点 (1)

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