Physical and Functional Recovery From Cardiac Surgery in Hospitalized Patients: A Feasibility Pilot Study

November 1, 2017 updated by: Baystate Medical Center
Ambulation following surgery has been found to be beneficial for patients; however, nurses and doctors struggle with getting post-operative, hospitalized patients to walk on their own. One promising strategy to address this might be an ambulation orderly, an employee whose single responsibility is to assure that patients walk 3-4 times per day. However, the effect of the ambulation orderly on post-operative physical activity has not yet been described. It is important to quantify what the ambulation orderly does in order to assess if this is an effective method for helping patients walk. As a result, the investigators will perform a pilot randomized controlled trial to test the effects of an ambulation orderly in patients hospitalized with recent cardiac surgery. Half of the patients will be assigned to walk with the ambulation orderly 3-4 times/day and the control group will be given standard nursing encouragement and assistance and encouragement to walk. The investigators will evaluate the average total daily step counts (over the hospital course, usually 4-7 days) and the change in walking distance between a baseline and a final 6 minute walk test. The investigators will also evaluate exercise physiologic parameters (heart rate, oxygen saturation) during ambulation, patient functional independence, and patient satisfaction.

Study Overview

Detailed Description

The investigators will perform a prospective randomized controlled trial at Baystate Medical Center, a 684-bed academic teaching hospital that serves as the referral center for a population of approximately 800,000 people living in Western Massachusetts.

The responsibility of the ambulation orderly is to walk patients after having a cardiac surgery, such as a coronary artery bypass surgery or a valve replacement or repair. Patients will be randomized to receive visits from the ambulation orderly (ambulation group) or to receive the standard care of Baystate Medical Center (control group). The standard of care will be nurse-directed ambulation, as is currently done in all other nursing floors at Baystate Medical Center. Nurses will be instructed to walk with the patients as they did before the initiation of the ambulation orderly and as they do when the orderly is on vacation, at conferences, training, or away for illness.

Study Type

Interventional

Enrollment (Actual)

36

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Massachusetts
      • Springfield, Massachusetts, United States, 01199
        • Baystate Medical Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Patients who have had a cardiac surgery procedure (coronary artery bypass grafting surgery or valve surgery). Must be ambulatory prior to surgery

Exclusion Criteria:

  • Unable to consent, cognitively impaired, and patients unable to walk prior to surgery

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Ambulation Orderly Intervention
Patients that are in this group are those randomized to receive visits from the ambulation orderly (ambulation group). The patients in this group will receive the visits from the ambulation orderly in addition to the standard of care that occurs with the rest of the hospital and with the control group.
The responsibility of the ambulation orderly is to walk patients after having a cardiac surgery, such as a coronary artery bypass surgery or a valve surgery. Baystate Medical Center hired an ambulation orderly May 8, 2013. The ambulation orderly is generally a high school graduate with some training in safe lifting and exercise, but extensive training is not required. In general, the goal is to have 1 ambulation orderly present 7 days a week for 8 hr per day. When available, ambulation orderlies are responsible for walking the patients who have been cleared by the clinical exercise physiologist or nurse up to 4 times per day. The walking of the patients occurs through the halls of the 6th floor of the Mass Mutual wing of Baystate Medical Center.
No Intervention: Control Group
This is for the patients who are randomized to receive the standard care of Baystate Medical Center. The standard of care will be nurse-directed ambulation, as is currently done in all other nursing floors at Baystate Medical Center. Nurses will be instructed to walk with the patients as they did before the initiation of the ambulation orderly and as they do when the orderly is on vacation, at conferences, training, or away for illness. These patients will not receive visits from the ambulation orderly.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Average Daily Step Counts while on M6 (cardiac surgery general floor.)
Time Frame: From arrival on M6 to hospital discharge. This is typically from post operative day 3 until post operative day 9-12.
The patient will wear an accelerometer, which will keep track of the amount of steps the patient took each day over the course of the hospitalization.
From arrival on M6 to hospital discharge. This is typically from post operative day 3 until post operative day 9-12.
Average change in walking distance between baseline and final 6-minute walk
Time Frame: From arrival on M6 (baseline) to hospital discharge (final). This is typically from post operative day 3 until post operative day 9-12
Each patient will complete a 6 minute walk after arriving on M6 (from intensive care until) and again at hospital discharge. The difference in distance walked will be compared.
From arrival on M6 (baseline) to hospital discharge (final). This is typically from post operative day 3 until post operative day 9-12

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Average Slope of Progression in Average Total Daily Step Counts
Time Frame: From arrival on M6 to hospital discharge. This is typically from post operative day 3 until post operative day 9-12.
The patient will wear an accelerometer, which will keep track of the amount of steps the patient took each day. The progression between groups will be compared.
From arrival on M6 to hospital discharge. This is typically from post operative day 3 until post operative day 9-12.
Average Daily Step Count on the 3rd day after arrival on M6
Time Frame: 3rd day on M6 as part of study (typically post operative day 6 or 7)
The step counts on the 3rd day after arrival on M6 will be compared in all groups. All patients are expected to still be in the hospital at this time.
3rd day on M6 as part of study (typically post operative day 6 or 7)
Average Total Daily Energy Expenditure
Time Frame: From arrival on M6 to hospital discharge. This is typically from post operative day 3 until post operative day 9-12.
The patient will wear an accelerometer, which will keep track of the total daily expenditure in calories per day.
From arrival on M6 to hospital discharge. This is typically from post operative day 3 until post operative day 9-12.
Average Total Time in Activity
Time Frame: From arrival on M6 to hospital discharge. This is typically from post operative day 3 until post operative day 9-12.
The patient will wear an accelerometer, which will keep track of the total time in activity.
From arrival on M6 to hospital discharge. This is typically from post operative day 3 until post operative day 9-12.
Pre and post 6 minute walk test vital signs
Time Frame: Each time the 6 minute walk test is done.
Heart rate, oxygen saturation, rating of perceived exertion, and rating of dyspnea will be measured before and after each 6 minute walk test.
Each time the 6 minute walk test is done.
Barthel Index
Time Frame: From arrival on M6 to hospital discharge. This is typically from post operative day 3 until post operative day 9-12.
The research staff and nurses or exercise physiologist will complete a survey to assess the physical independence of the patients.
From arrival on M6 to hospital discharge. This is typically from post operative day 3 until post operative day 9-12.
Hospital Consumer Assessment of Healthcare Providers and Systems (HCAHPS) Survey
Time Frame: Following the hospital stay within 2-6 weeks
The HCAHPS survey will be given to each patient at discharge to mail back to assess the overall satisfaction in each group.
Following the hospital stay within 2-6 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Collaborators

Investigators

  • Study Director: Peter Lindenauer, MD, MSc, Baystate Medical Center

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

March 1, 2015

Primary Completion (Actual)

July 1, 2015

Study Completion (Actual)

July 1, 2016

Study Registration Dates

First Submitted

January 27, 2015

First Submitted That Met QC Criteria

February 24, 2015

First Posted (Estimate)

March 2, 2015

Study Record Updates

Last Update Posted (Actual)

November 6, 2017

Last Update Submitted That Met QC Criteria

November 1, 2017

Last Verified

November 1, 2017

More Information

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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