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OpenTrials
Completed

NCT Number: NCT01295541

Early Progressive Mobility in the CVICU: Assessing Current Status

The current study is proposed to assess the frequency and type of progressive mobility procedures currently performed in the CVICU The study will evaluate the type and frequency of progressive mobility orders, whether or not progressive mobility steps are being taken by the nursing teams, define what steps patients are receiving, and record time to first weight bearing. Other outcome measures will be the days of required mechanical ventilation, and current ICU length of stay and cost to treat.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Medical College of Central Georgia

Macon, Georgia, 31201, United States

About this study

This will be a descriptive 4 month study of standard care practice. Patients who meet the inclusion / exclusion criteria for study will be enrolled (Waiver of informed consent is requested) and followed for a maximum of 28 days. The type and frequency of progressive mobility orders, whether or not progressive mobility steps are being taken by the nursing teams, define what steps patients are receiving, and record time to first weight bearing will be recorded. Weight bearing will be defined as standing for at least 1 minute. ICU LOS, Ventilator Days will be assessed at ICU discharge for study patients. Barriers to PM procedures will also be assessed.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patient is ≥ 18 years old.
  • Patient has been admitted to the ICU for less than 3 days prior to study enrollment
  • Patients require mechanical ventilation for >48 hours

Exclusion criteria

  • Mobilization is contraindicated by Patient's condition. Such as hip fractures or other injury that would impede standing posture.
  • Patient weighs less than 70 pounds or more than 440 pounds
  • Mobilization is contraindicated by patient's condition or physician's orders exist that prevent the patient from participating in the mobility protocol.
  • Patient was unable to walk or stand without assistance prior to ICU admission.
  • Patient was cognitively unable to follow verbal commands prior to ICU admission.
  • Patients current diagnosis includes acute stroke with neurologic impairment
  • Patient's current diagnosis includes drug overdose.
  • Patient has "Do not resuscitate" orders and/or is at an end stage terminal disease state.
  • Patient requires a specialty bed or mattress.

Treatment and study plan

Primary outcomes

  1. First OOB

    Time frame: Days

    The ICU day that the patient is able to stand for at least 1 minute will be assessed.

Secondary outcomes

  1. ICU LOS

    Time frame: Days

    Length of stay will be measured

  2. Type and Frequency of PM orders

    Time frame: Daily

    The type and frequency of Progressive mobility orders will be assessed

Sponsors and collaborators

Lead sponsor

Hill-Rom

Industry

Registry information

Important dates

Study start
2010
Primary completion
2010
Study completion
2010
First posted
Feb 14, 2011
Registry last updated
Feb 14, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.