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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03473353
Other study ID # STUDY00007664
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 30, 2017
Est. completion date December 31, 2022

Study information

Verified date January 2023
Source Milton S. Hershey Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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 information / eligibility

Status Completed
Enrollment 732
Est. completion date December 31, 2022
Est. primary completion date June 29, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Provider Participants 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


Related Conditions & MeSH terms


Intervention

Other:
Medical Scribe
Trained Medical Scribes will be present in the exam room to take notes on the the electronic medical record so that clinicians can focus all their attention to the interaction with the patient and parent.

Locations

Country Name City State
United States Hope Drive Pediatric Clinic Hershey Pennsylvania

Sponsors (1)

Lead Sponsor Collaborator
Milton S. Hershey Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Clinician Burnout Survey questions will assess clinician burnout using validated measures. 1 year
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