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CompletedNCT02209558SternalUpdated Apr 14, 2015

The Effect of Visual Sternal Precautions on Behavioral Intentions and Readmissions

An interventional study of Visual Sternal Precautions in Intention - Mental Process and Readmission Rates, sponsored by Northwell Health. Completed at 1 site in United States. Per ClinicalTrials.gov, last updated 2015-04-14.

Sponsored by Northwell Health · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
19
Allocation
Randomized
Sex
All
01

Study summary

Sternal precautions are standard patient education protocol disseminated to post-operative open heart surgery patients . While this "best practice" safety measure is widely distributed to patients, the origin of said precautions is unknown. Statewide hospitals vary on their parameters for sternal precautions using a myriad of restrictions, i.e. weighted activities, biomechanical movements to be avoided. In addition, the medium in which sternal precautions are taught varies, thus complicating patient adherence to these vital post-operative measures.

The primary objective of this study is to use a randomized pre-post test design to compare two different training procedures. One training group examines current standard of care (providing verbal instruction using teach back and written sternal precautions). The second training group provides subjects with visual depiction of sternal precautions, in addition to standard of care. The study will analyze 30 and 60 day readmission rates for aforementioned patients. Finally, the study will assess changes in behavior intentions from before training to after training in both groups via behavioral analysis survey consisting of 8 questions.

Hypothesis 1: The investigators hypothesize that subjects provided with visual sternal precautions, in addition to standard of care, will have a lower 30 and 60 day readmission rate when compared to subjects in the standard of care group

Hypothesis 2: The investigators hypothesize that changes in behavior intentions toward sternal precautions will be greater from before training to after training in the visual SPs in addition to standard of care group than the standard of care only group.

Read the detailed description

Eligible subjects will be identified by the Senior Cardiothoracic Physical Therapist (Dr. Craig D. Feinman, PT, DPT) on staff at North Shore University Hospital. Dr. Feinman will provide basic study information to potential subjects and refer those that are interested in the study to the research team who will then provide a copy of the consent form and more information about the study. Inclusion Criteria represents post-surgical adult patients who had a median or midline sternotomy incision during cardiac surgery at North-Shore University Hospital. Exclusion Criteria represents patients with dementia or those that are cognitively impaired will be excluded from the study.

A T-test or Mann Whitney U test will be use to compare group differences on continuous variables, e.g. age. Beta regression or logistic regression model will be developed for the outcomes of adherence and readmission proportions/rates. To assess changes from pre to post training on behavioral intentions a paired t-test or Wilcoxon signed rank for matched pairs will be used. A result will be considered statistically significant at the p\<0.05 level of significance. All analyses will be performed using SAS version 9.3 (SAS Institute, Cary, NC).

02

Conditions studied

  • Intention - Mental Process
  • Readmission Rates
03

In context

Lead sponsor

Northwell Health is the lead sponsor of 463 studies on the registry; 109 are open to participants now.

Of its 40 completed or terminated interventional studies of FDA-regulated products, 20 (50%) have results posted.

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

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Post-surgical adult patients who had a median or midline sternotomy incision during cardiac surgery at North-Shore University Hospital.

Exclusion criteria

Exclusion Criteria:

  • Patients with dementia or those that are cognitively impaired will be excluded from the study.
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
19 participants (actual)

Study arms

  • No intervention
    Standard Written Sternal Precautions

    Patients will receive education that is the "standard of care" at North Shore Long Island Jewish Health Systems in their post-operative sternal precautions.

  • Experimental
    Visual Sternal Precautions

    Patients will receive both "standard of care" written sternal precautions, as well as visual sternal precautions.

    Behavioral: Visual Sternal Precautions

Interventions

  • BehavioralVisual Sternal Precautions

    Visual depiction of SPs in addition to "standard of care" written precautions

06

What researchers measure

Primary outcomes

  1. Patient behavioral intentions post visual training strategies

    The intervention group will receive "standard of care" sternal precautions delivered via written medium. In addition, printed visual depictions of sternal precautions will be provided. During completion of the initial Physical Therapy evaluation, patients will be asked to provide baseline knowledge of sternal precautions via "teach back," an important tool in assessing patients' knowledge of important points delivered during clinical practice. Patients will then perform teach back of sternal precautions upon second Physical Therapy encounter to ensure understanding and post-operative anesthesia effects have waned. Prior to discharge (when patient deemed medically appropriate by the medical/surgical team), the patient will receive a survey consisting of 8 behavioral intention questions with "yes," "no," or "not sure" responses. Questions posed on the surveys assess if patients will/will not perform certain behaviors that may/may not predispose a risk to the patient's sternum.

    Time frame: Post-operative day one when patient medically cleared for PT evaluation, 2nd session, and prior to discharge from hospital (approximately 1-10 days)

Secondary outcomes

  1. 30 and 60 day readmission rates

    Re-admission rates of enrolled subjects is integral in determining if patients adhere to sternal precautions after discharge. Resumption of regular activities is cleared by the medical/surgical team. The study team will review the medical records of the subjects 60 days after enrollment to determine if and why they were re-admitted to the hospital. Since there is a possibility for subjects to be re-admitted to facilities outside of the health system, the study team will also call the enrolled subjects 60 days after enrollment to obtain this information.

    Time frame: 30-60 days post patient discharge from hospital setting

07

Study locations

1 site
  • North Shore University Hospital
    Manhasset, New York 11030, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 14, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02209558
Lead sponsor
Northwell Health
Collaborators
North Shore University Hospital
Responsible party
Craig Feinman (Senior Cardiothoraic Physical Therapist, Physical Therapy, Northwell Health) — Principal investigator
First posted
Aug 6, 2014
Start date
Aug 2014
Primary completion
Apr 2015
Completion
Apr 2015
Last update
Apr 14, 2015

Study contacts

Craig D Feinman, Doctor of Physical Therapy
principal investigator · North Shore University Hospital, NSLIJ Health System
Renee Pekmezaris, PhD
study director · North Shore University Hospital, NSLIJ Health System
Andrzej Kozikowski, PhD
study director · North Shore University Hospital, NSLIJ Health System
Jonathan Dropkin, ScD, PT
study director · North Shore University Hospital, NSLIJ Health System
Joanna Steinn, MPH
study director · North Shore University Hospital, NSLIJ Health System
Alan Hartman, MD
study director · North Shore University Hospital, NSLIJ Health System

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2015. You cannot join it, but the record below documents what was studied.

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