NCT02771431

Brief Summary

Our study would be the first randomized study investigating the use of video conferencing via tablet computers versus traditional bedside rounding and its effect on clinical data such as length of stay and complications as well as patient satisfaction. As technology improves, medicine has an obligation to incorporate this technology to improve efficiency and cost-effectiveness. If telerounding is proven to not change outcomes or patient satisfaction, it saves time for the physician during office hours to see more patients or be productive in other ways. Telerounding could be applied in remote areas with a dearth of specialists, allowing these specialists' expertise to reach areas it could not before.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
107

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Feb 2015

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2015

Completed
1.1 years until next milestone

First Submitted

Initial submission to the registry

February 22, 2016

Completed
3 months until next milestone

First Posted

Study publicly available on registry

May 13, 2016

Completed
2.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 13, 2018

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 13, 2018

Completed
Last Updated

August 8, 2019

Status Verified

August 1, 2019

Enrollment Period

3.8 years

First QC Date

February 22, 2016

Last Update Submit

August 6, 2019

Conditions

Outcome Measures

Primary Outcomes (4)

  • Complication rates

    4 years

  • length of inpatient stay

    4 years

  • number of lab tests ordered

    4 years

  • severity of complications

    4 years

Secondary Outcomes (1)

  • Additionally patient satisfaction will be looked at based on post-operative questionnaire.

    4 years

Study Arms (2)

Standard

NO INTERVENTION

Group 1 will consist of patients receiving in-person attending-patient encounters while inpatients.

Tele-rounding

EXPERIMENTAL

Group 2 will consist of patients receiving video-conference attending-patient encounters. The intervention is being seen via ipad

Other: Tele-rounding in post operative care

Interventions

Both groups will receive standard of care. The only difference between these groups would be the physical presence of the attending in the room. Both groups will receive a physical exam with supervision of the attending, one group will have attending in the room and the other will have the attending present via I-pad. In both cases if there was something of concern the attending would step in for the physical exam if needed, regardless of which group they were randomized for.

Tele-rounding

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Patients 18 years of age or older
  • Undergo elective Urologic surgery requiring post-operative inpatient stay

You may not qualify if:

  • Patients under 18 years of age
  • Patients who are unable to provide their own consent
  • Patients who undergo urgent or emergent Urologic procedures who are not already enrolled in the study
  • Patients who do not require an inpatient post-operative stay
  • Patients who are seen on the weekend (Saturday or Sunday)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

North Shore LIJ

New Hyde Park, New York, 11042, United States

Location

Related Publications (7)

  • Strehle EM, Shabde N. One hundred years of telemedicine: does this new technology have a place in paediatrics? Arch Dis Child. 2006 Dec;91(12):956-9. doi: 10.1136/adc.2006.099622.

    PMID: 17119071BACKGROUND
  • Lilly CM, Cody S, Zhao H, Landry K, Baker SP, McIlwaine J, Chandler MW, Irwin RS; University of Massachusetts Memorial Critical Care Operations Group. Hospital mortality, length of stay, and preventable complications among critically ill patients before and after tele-ICU reengineering of critical care processes. JAMA. 2011 Jun 1;305(21):2175-83. doi: 10.1001/jama.2011.697. Epub 2011 May 16.

    PMID: 21576622BACKGROUND
  • Young LB, Chan PS, Lu X, Nallamothu BK, Sasson C, Cram PM. Impact of telemedicine intensive care unit coverage on patient outcomes: a systematic review and meta-analysis. Arch Intern Med. 2011 Mar 28;171(6):498-506. doi: 10.1001/archinternmed.2011.61.

    PMID: 21444842BACKGROUND
  • Ellison LM, Pinto PA, Kim F, Ong AM, Patriciu A, Stoianovici D, Rubin H, Jarrett T, Kavoussi LR. Telerounding and patient satisfaction after surgery. J Am Coll Surg. 2004 Oct;199(4):523-30. doi: 10.1016/j.jamcollsurg.2004.06.022.

    PMID: 15454133BACKGROUND
  • Ellison LM, Nguyen M, Fabrizio MD, Soh A, Permpongkosol S, Kavoussi LR. Postoperative robotic telerounding: a multicenter randomized assessment of patient outcomes and satisfaction. Arch Surg. 2007 Dec;142(12):1177-81; discussion 1181. doi: 10.1001/archsurg.142.12.1177.

    PMID: 18086984BACKGROUND
  • Gandsas A, Parekh M, Bleech MM, Tong DA. Robotic telepresence: profit analysis in reducing length of stay after laparoscopic gastric bypass. J Am Coll Surg. 2007 Jul;205(1):72-7. doi: 10.1016/j.jamcollsurg.2007.01.070.

    PMID: 17617335BACKGROUND
  • Kaczmarek BF, Trinh QD, Menon M, Rogers CG. Tablet telerounding. Urology. 2012 Dec;80(6):1383-8. doi: 10.1016/j.urology.2012.06.060.

    PMID: 23206790BACKGROUND

Study Officials

  • Manish Vira, MD

    Physician

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Attending Urologist

Study Record Dates

First Submitted

February 22, 2016

First Posted

May 13, 2016

Study Start

February 1, 2015

Primary Completion

November 13, 2018

Study Completion

November 13, 2018

Last Updated

August 8, 2019

Record last verified: 2019-08

Locations