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Doctor-Parent Interactions With Medical Scribes

Not Applicable
Completed
Conditions
Burnout, Professional
Interventions
Other: Medical Scribe
Registration Number
NCT03473353
Lead Sponsor
Milton S. Hershey Medical Center
Brief Summary

The purpose of the study is to collect outcomes related to a quality improvement project assessing the feasibility and effectiveness of a medical scribe program in which medical scribes accompany clinicians during their visits with patients. The medical scribes involved in the project are professional scribes and medical students who will accompany clinicians during patient visits and takes notes, enabling the clinician to engage more directly with the patient.

Detailed Description

The study has several specific objectives. This study aims to examine the impact of using medical scribes on (1) patient experience (e.g. patient satisfaction) (2) clinician experience (e.g. stress load, burnout, evaluation of the visit, amount of time spent after hours inputting notes), and (3) clinician-patient interaction (e.g. patient and clinician engagement during the visit).

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
732
Inclusion Criteria
  1. Attending clinicians with privileges at Penn State Hershey Children's Hospital and/or the Penn State Hershey Internal Medicine. This may include attending MDs or DOs and Nurse Practitioners (NPs).
  2. Voluntary participation in the medical scribe QI project.
  3. Consents to participate in the study.
Exclusion Criteria
  1. Clinician is not participating in the scribe project.
  2. Clinician does not consent to participate in the research portion of this project.

Patient Participants

Inclusion Criteria:

  1. Patient (if 18 years or older) or parent/guardian (P/G) of patient being seen by a participating clinician.
  2. Patient was not seen by a resident or medical student prior to meeting with clinician.
  3. English speaking/reading.
  4. Patient or P/G has capacity to consent.

Exclusion Criteria:

  1. Patient is seeing a clinician who has not consented to participate in the research portion of the study.
  2. Non-English speaking/reading.
  3. Patient or P/G lacks capacity to consent.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Pediatric CliniciansMedical ScribeSurvey data will be gathered from pediatric clinicians and also parents of pediatric patients at two time periods. At baseline, no Medical Scribes will be working with the clinicians, and then several months later, data will be gathered when Medical scribes ARE working with clinicians.
Primary Outcome Measures
NameTimeMethod
Clinician Burnout1 year

Survey questions will assess clinician burnout using validated measures.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Hope Drive Pediatric Clinic

🇺🇸

Hershey, Pennsylvania, United States

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