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The Effect of Visual Sternal Precautions on Behavioral Intentions and Readmissions (Sternal Trial)

N/A
Waitlist Available
Led By Craig D Feinman, Doctor of Physical Therapy
Research Sponsored by Northwell Health
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
* Post-surgical adult patients who had a median or midline sternotomy incision during cardiac surgery at North-Shore University Hospital.
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 30-60 days post patient discharge from hospital setting
Awards & highlights
No Placebo-Only Group

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.

Eligible Conditions
  • Intentionality
  • Readmission Rates

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~30-60 days post patient discharge from hospital setting
This trial's timeline: 3 weeks for screening, Varies for treatment, and 30-60 days post patient discharge from hospital setting for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Patient behavioral intentions post visual training strategies
Secondary study objectives
30 and 60 day readmission rates

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Visual Sternal PrecautionsExperimental Treatment1 Intervention
Patients will receive both "standard of care" written sternal precautions, as well as visual sternal precautions.
Group II: Standard Written Sternal PrecautionsActive Control1 Intervention
Patients will receive education that is the "standard of care" at North Shore Long Island Jewish Health Systems in their post-operative sternal precautions.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Visual Sternal Precautions
2014
N/A
~20

Find a Location

Who is running the clinical trial?

North Shore University HospitalOTHER
13 Previous Clinical Trials
3,660 Total Patients Enrolled
Northwell HealthLead Sponsor
475 Previous Clinical Trials
469,265 Total Patients Enrolled
Craig D Feinman, Doctor of Physical TherapyPrincipal InvestigatorNorth Shore University Hospital, NSLIJ Health System
Renee Pekmezaris, PhDStudy DirectorNorth Shore University Hospital, NSLIJ Health System
2 Previous Clinical Trials
344 Total Patients Enrolled
Andrzej Kozikowski, PhDStudy DirectorNorth Shore University Hospital, NSLIJ Health System
Jonathan Dropkin, ScD, PTStudy DirectorNorth Shore University Hospital, NSLIJ Health System
Joanna Steinn, MPHStudy DirectorNorth Shore University Hospital, NSLIJ Health System
Alan Hartman, MDStudy DirectorNorth Shore University Hospital, NSLIJ Health System
~2 spots leftby Jan 2026