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N/A N=40 Randomized Diagnostic

Evaluation of a Pocket-Sized Ultrasound Device As an Aid to the Physical Examination

Splenomegaly · Pleural Effusion

Enrolled (actual)
40
Serious AEs
0.0%
Results posted
Feb 2015
Primary outcome: Primary: Comparison of Diagnostic Ability of the Intervention Group's Ultrasound Exam to the Control Group's Physical Exam — 6.4; 7.6; 79.6; 79.3 units on a scale — p=0.11

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
resident with GE vscan (Device)
Age
Adult · 24+ yrs
Sex
All
Sponsor
Brigham and Women's Hospital
Primary completion
Nov 2012

Outcome Measures

OutcomeResultp-value
PRIMARY
Comparison of Diagnostic Ability of the Intervention Group's Ultrasound Exam to the Control Group's Physical Exam
6.4; 7.6; 79.6; 79.3 0.11
SECONDARY
Improvement in Diagnostic Ability Within the Intervention Group
6.7; 7.6; 79.3; 79.1 0.043 sig

Summary

The 40 resident study subjects will be randomized to either receive a training session on use of a pocket-sized ultrasound or to receive training on physical exam skills. Following these sessions the subjects will have the opportunity to practice their skills during clinical rounds at BWH inpatient and outpatient settings. Four weeks after the training session all study subjects will take part in an assessment of their diagnostic skills. During this assessment they will be asked to complete an exam on a patient subject. Those randomized to the ultrasound group will be allowed to use their devices while the control group will use the traditional physical exam. Following the exams, resident study subjects will be asked to indicate whether they detected any of the following abnormalities on their exams: pleural effusion, hepatomegaly, cirrhotic liver, splenomegaly, ascites, aortic stenosis, mitral regurgitation, right atrial pressure, abdominal aortic aneurysm, deep vein thrombosis. Resident study subjects will also complete a questionnaire about the physical exam and use of the ultrasound. Prior to the assessment, all patients will undergo ultrasound by an attending radiologist, and these results will serve as the "gold standard" for our study.

Eligibility Criteria

Inclusion Criteria

  • All interns and residents in the BWH internal medicine residency program who responded to a recruitment email and agreed to participate.

Exclusion Criteria

  • • Radiology Preliminary residents
  • Residents with previous formalized ultrasound training that included a practical component
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01948076). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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