CClinicalTrials.gg
CompletedNCT01576614Updated Sep 26, 2013

The Role of Off-shift Robotic Telerounding Between Physicians and Nurses in the Surgical Intensive Care Unit

An observational study in Off-shift Robotic Telerounding, sponsored by Lahey Clinic. Completed at 1 site in United States. Open to participants aged 18 Years to 75 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2013-09-26.

Sponsored by Lahey Clinic · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
35
Ages
18 Years to 75 Years
Sex
All
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Study summary

Hypothesis: The use of a mobile robotic telepresence system for off-hours rounding in the surgical intensive care unit has an impact on nurse-physician collaboration.

Study question: Does the addition of mobile video communication provided by RTP affect nurse-physician collaboration during off shift rounding in the surgical intensive care unit when compared to the more common clinical practice of off-shift rounding using the telephone?

Read the detailed description

This is a mixed-method study, involving both surveys and ethnographic fieldwork. The research team will utilize the Collaboration and Satisfaction About Care Decisions (CSACD) survey instrument at regular intervals to assess nurse-physician collaboration. The instrument is validated and reliable and has been extensively tested. Permission was obtained to use the instrument. The ethnographic investigation will run concurrently and be performed by a doctoral student from Massachusetts Institute of Technology (MIT). No part of the study will involve patient intervention. The study will be conducted in the surgical intensive care unit (SICU).

The survey-based portion of the study is a prospective, randomized, crossover-controlled trial; it will generate ordinal data regarding nurse-physician collaboration and satisfaction. The ethnographic portion of the study will involve observation and interviews. The MIT student will engage in unobtrusive observational shadowing of APs and nurses throughout the study, and will formally interview each observed AP and nurse twice during the entire length of the study: once at the onset of the study, and once as the study draws to conclusion. This observational shadowing will include visits to the SICU. All participants will be consented for the study. Consent for and implementation of these methods will be undertaken in a manner consistent with current best research practice; extensive measures will be taken to protect staff confidentiality.

02

Conditions studied

  • Off-shift Robotic Telerounding

Keywords

  • Comparing telephone VS RTP in SICU rounding practices
03

In context

Lead sponsor

Lahey Clinic is the lead sponsor of 58 studies on the registry; 4 are open to participants now.

Of its 5 completed or terminated interventional studies of FDA-regulated products, 4 (80%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Full time Nursing and Physician Staff providing rounding services in the Surgical Intensive Care Unit

Inclusion criteria

  • Full time registered nursing staff
  • Resident physicians and critical care attending physicians

Exclusion criteria

Exclusion Criteria:

  • Non-registered nursing staff
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
35 participants (actual)

Groups and cohorts

  • Nurse-Physician Rounding by Phone

    The SICU's practice involves daily morning team rounding at the bedside. The team includes the critical care attending physician (AP), surgical resident physician, and critical care nurse. The AP is physically present in the SICU during these rounds and for the hours between approximately 7am and 7pm. During off-shift hours (7pm-7am), the AP is available by phone as the "on-call" attending physician. In addition to this on-call availability, the standard of practice in SICU for years has been that the on-call physician proactively places a telephone call to the SICU at least once every evening to perform "telephone rounds" with the resident physician aeach SICU patient.

    Behavioral: Remote physician rounding

  • Nurse-Physican rounding by R T P

    Remote Telepresence Robotics (RTP) is a form of telemedicine that enables a fast and direct face-to-face response by a physician, located remotely, and may sometime utilize a mobile robot. RTP provides the physician the ability to teleconference with patients and other healthcare providers using two way audio visual technology. The sophistication of these devices varies and can range from simple video conferencing to remote robotic control devices with audio visual conferencing capabilities. The "robotic" capabilities refer to ability of the physician to remotely direct or drive the device from one location to another. The technology allows clinical experts to provide the right care at the right time and has become an accepted standard of care when used under appropriate circumstances.

    Behavioral: Remote physician rounding

Interventions

  • BehavioralRemote physician rounding

    Use of Remote physician rounding using Remote Telepresence Robotics

    Also known as: RTP, Remote Telepresence Rounding, Telemedicne, Robotic rounds

06

What researchers measure

Primary outcomes

  1. Collaboration and Satisfaction Survey About Care Decisions using CSACD Scores

    This is a mixed-method study, involving both surveys and ethnographic fieldwork. The research team will utilize the Collaboration and Satisfaction About Care Decisions (CSACD) survey instrument at regular intervals to assess nurse-physician collaboration. The instrument is validated and reliable and has been extensively tested. Permission was obtained to use the instrument

    Time frame: One Year

07

Study locations

1 site
  • Lahey Clinic
    Burlington, Massachusetts 01805, United States
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References and documents

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 26, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01576614
Lead sponsor
Lahey Clinic
Responsible party
Sponsor
First posted
Apr 12, 2012
Start date
Aug 2011
Primary completion
Aug 2013
Completion
Sep 2013
Last update
Sep 26, 2013

Study contacts

Timothy N. Liesching, MD
principal investigator · Lahey Clinic

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2013. You cannot join it, but the record below documents what was studied.

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