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Clinical Trials/NCT03988751
NCT03988751CompletedNot Applicable

Real-time Location System Feasibility Study Part 2

Wake Forest University Health Sciences2 sites in 1 country22 target enrollmentStarted: June 6, 2019Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
22
Locations
2
Primary Endpoint
Characterize Number of Participants Who Tolerate Continuous vs Interval 40m Walk.

Study Overview

Brief Summary

The proposed study will investigate the feasibility of using the Wake Forest Real-time Location System (RTLS) in monitoring patient movement during their in-hospital postoperative recovery. The study will involve patients who have undergone surgery requiring inpatient admission to the surgical ward. Actual patient movement will be monitored during their postoperative recovery and compared with data recorded by the Wake Forest location system.

In this small pilot study, a subgroup of participants will be randomized to two cohorts, continuous walking and interval walking. Tolerability of the varied walking intensity will be measured.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
Single (Investigator)

Eligibility Criteria

Ages
18 Years to 90 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Characterize Number of Participants Who Tolerate Continuous vs Interval 40m Walk.

Time Frame: 1 day

Characterize number of participants who tolerate continuous vs interval 40m walk by evaluation of adverse events and change in vital signs.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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