Virtual Visits at Brigham and Women's Hospital

Sponsor
Brigham and Women's Hospital (Other)
Overall Status
Terminated
CT.gov ID
NCT03592355
Collaborator
(none)
77
1
2
22.6
3.4

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Virtual Visit
N/A

Detailed Description

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.

Again, aside from the initial randomization and retrospective data collection and analysis, all of the above would have occurred irrespective of this research protocol.

Study Design

Study Type:
Interventional
Actual Enrollment :
77 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
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).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).
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Virtual Visits at Brigham and Women's Hospital: A Randomized Controlled Trial
Actual Study Start Date :
Apr 13, 2018
Actual Primary Completion Date :
Mar 1, 2020
Actual Study Completion Date :
Mar 1, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention

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

Other: Virtual Visit
Clinicians will have a synchronous video visit with their patients.

No Intervention: Control

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

Outcome Measures

Primary Outcome Measures

  1. Days until third available appointment [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.

Secondary Outcome Measures

  1. Days until first available appointment [Through study completion, an average of 6 months]

    Number of days until the next 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 next available routine appointment.

  2. Future capacity: percentage of open appointment slots [Through study completion, an average of 6 months]

    Percentage of appointment slots that are open and available for booking patients over the next four weeks, obtained at 12 o'clock each Friday (embargoed appointments not included). The mean of all of the weeks is a clinician's future capacity.

  3. Frequency of visits with the usual provider of care [Through study completion, an average of 6 months]

    Ratio of the number of visits to the most frequently seen provider to the total number of visits to all providers obtained each month. The mean of all of the months is a clinician's ratio.

  4. Continuity of care index [Through study completion, an average of 6 months]

    The number of visits to each individual physician divided by the total number of visits the patient had overall obtained each month. The mean of all of the months is the continuity of care index

  5. No show rate [Through study completion, an average of 6 months]

    Ratio of the number of no-show visits to total visit slots obtained each week. The mean of all of the weeks is a clinician's no show rate.

  6. Visit time [Through study completion, an average of 6 months]

    In-person: face time with patient per pertinent EHR fields, obtained each week. The mean of all of the weeks is a clinician's visit time. Virtual: enter virtual waiting room to video stops, obtained each week. The mean of all of the weeks is a clinician's visit time.

  7. Clinician volume per hour [Through study completion, an average of 6 months]

    Patients seen per hour, calculated at the end of the study.

  8. Clinician volume per day [Through study completion, an average of 6 months]

    Patients seen per day, all calculated at the end of the study.

  9. Clinician volume per month [Through study completion, an average of 6 months]

    Patients seen per month, all calculated at the end of the study.

  10. Clinician volume per 6 months [Through study completion, an average of 6 months]

    Patients seen per 6 months, all calculated at the end of the study.

  11. Slot utilization [Through study completion, an average of 6 months]

    Ratio of used slots to total slots, obtained each week. The mean of all of the weeks is a clinician's slot utilization.

  12. Number of primary care visits [Through study completion, an average of 6 months]

    Number of primary care visits

  13. Number of specialist visits [Through study completion, an average of 6 months]

    Number of specialist visits

  14. Number of emergency department visits [Through study completion, an average of 6 months]

    Number of emergency department visits

  15. Number of inpatient admissions [Through study completion, an average of 6 months]

    Number of inpatient admissions

  16. Number of imaging studies [Through study completion, an average of 6 months]

    Number of imaging studies ordered

  17. Number of labs ordered [Through study completion, an average of 6 months]

    Number of laboratory studies ordered

  18. Number of medications prescribed [Through study completion, an average of 6 months]

    Number of medications prescribed

  19. Patient Experience [Sent electronically within 1 week of the in-person or virtual visit]

    Brigham Health Virtual Care team survey sent to participating patients

  20. Revenue from virtual or in-person visit [Through study completion, an average of 6 months]

    Revenue garnered by an individual clinician for her/his clinical activity, calculated per hour and per 6 months (denominator: total clinical hours worked).

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Clinician whose department is chosen for virtual visit rollout
Exclusion Criteria:
  • Clinician who saw on average fewer than 20 patients monthly over the past 6 months

  • Clinician who opts out of virtual visits

Contacts and Locations

Locations

Site City State Country Postal Code
1 Brigham and Women's Hospital Boston Massachusetts United States 02115

Sponsors and Collaborators

  • Brigham and Women's Hospital

Investigators

  • Principal Investigator: David Levine, MD, MPH, MA, Principal Investigator

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
David Levine, Associate Physician, Brigham and Women's Hospital
ClinicalTrials.gov Identifier:
NCT03592355
Other Study ID Numbers:
  • 2018P000452
First Posted:
Jul 19, 2018
Last Update Posted:
Sep 22, 2021
Last Verified:
Sep 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by David Levine, Associate Physician, Brigham and Women's Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 22, 2021