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临床试验/NCT03592355
NCT03592355终止不适用

Virtual Visits at Brigham and Women's Hospital: A Randomized Controlled Trial

Brigham and Women's Hospital2 个研究点 分布在 1 个国家目标入组 77 人开始时间: 2018年4月13日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
77
试验地点
2
主要终点
Days until third available appointment

研究概览

简要总结

Clinicians slated for virtual visit rollout will be randomized (stratified by department) to either receive immediate virtual visit on-boarding (intervention arm) or delayed (3-months later) virtual visit on-boarding (control arm). The investigators plan to enroll no more than 200 clinicians.

Any clinician in a department selected by the Brigham Health Virtual Care team for access to virtual visits is eligible, unless s/he saw less than 20 patients monthly over the last 6 months.

The Brigham Health Virtual Care team will onboard all clinicians and provide virtual visit support as per their usual protocol. The primary study endpoint is third-available appointment, a well-adopted measure of access. Other secondary endpoints revolve around continuity, efficiency, utilization, safety, cost, and patient experience.

详细描述

If enrolled in the intervention arm, the following steps will occur:

  • The clinician will receive the intervention arm follow-up email ("Follow-up Email - Intervention" in the Appendix).
  • The Brigham Health Virtual Care team will work with the clinician toward immediate on-boarding (software training, hardware setup, technical support) as per their usual process.
  • The clinician will schedule virtual visits as s/he and/or her/his department see fit. Virtual visits occur on an already-in-use Partners- and Brigham-approved video platform (attached).

If enrolled in the control arm, the following steps will occur:

  • The clinician will receive the control arm follow-up email ("Follow-up Email - Control" in the Appendix).
  • Three months from the time of the follow-up email, the Brigham Health Virtual Care team will work with the clinician toward immediate on-boarding (software training, hardware setup, technical support) as per their usual process.
  • The clinician will schedule virtual visits as s/he and/or her/his department see fit. Virtual visits occur on an already-in-use Partners- and Brigham-approved video platform (attached).

The investigators plan to follow patients of both clinician cohorts for a total of 6-months. The investigators will perform retrospective review of patient electronic health records and patients will receive a redcap survey (attached), an evaluation mechanism already employed by the Virtual Care team.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Clinician whose department is chosen for virtual visit rollout

排除标准

  • Clinician who saw on average fewer than 20 patients monthly over the past 6 months
  • Clinician who opts out of virtual visits

结局指标

主要结局

Days until third available appointment

时间窗: Through study completion, an average of 6 months

Number of days until the third available routine appointment, obtained at 12 o'clock each Friday (embargoed appointments not included). The mean of all of the weeks is a clinician's average number of days until the third available routine appointment.

次要结局

  • Number of inpatient admissions(Through study completion, an average of 6 months)
  • Frequency of visits with the usual provider of care(Through study completion, an average of 6 months)
  • Visit time(Through study completion, an average of 6 months)
  • Clinician volume per day(Through study completion, an average of 6 months)
  • Number of labs ordered(Through study completion, an average of 6 months)
  • Days until first available appointment(Through study completion, an average of 6 months)
  • Clinician volume per hour(Through study completion, an average of 6 months)
  • Number of specialist visits(Through study completion, an average of 6 months)
  • Continuity of care index(Through study completion, an average of 6 months)
  • Clinician volume per 6 months(Through study completion, an average of 6 months)
  • Patient Experience(Sent electronically within 1 week of the in-person or virtual visit)
  • Future capacity: percentage of open appointment slots(Through study completion, an average of 6 months)
  • Slot utilization(Through study completion, an average of 6 months)
  • Number of emergency department visits(Through study completion, an average of 6 months)
  • Number of medications prescribed(Through study completion, an average of 6 months)
  • No show rate(Through study completion, an average of 6 months)
  • Clinician volume per month(Through study completion, an average of 6 months)
  • Number of primary care visits(Through study completion, an average of 6 months)
  • Number of imaging studies(Through study completion, an average of 6 months)
  • Revenue from virtual or in-person visit(Through study completion, an average of 6 months)

研究者

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

David Levine

Associate Physician

Brigham and Women's Hospital

研究点 (2)

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