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The Patient's Experience With Physician Assistant Providers (PEPAP)

The Patient's Experience With Physician Assistant Providers: a Descriptive Survey and Randomized Intervention

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05104879
Acronym
PEPAP
Enrollment
192
Registered
2021-11-03
Start date
2021-12-31
Completion date
2022-02-28
Last updated
2021-11-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Joint Diseases, Midlevel Providers, Nurse Practitioners, Physician Assistants, Patient Perceptions, Patient Preferences

Brief summary

Our investigation was a prospective cross-sectional survey evaluating the patient experience to new patients that presented to an outpatient private practice specialized in total joint reconstruction. New patients seeing a PA during their initial visit were randomized to intervention and control groups and all were given a descriptive survey at checkout. Inclusion criteria (1) new patient (2) English speaking (3) appointment with PA. There was no exclusion criteria. Eligible patients were randomized to the intervention group (received biosketch card) or the control group (no card) using random number generator. Patients within the intervention group received a biosketch card during rooming, pre-clinician encounter, and were not informed about involvement. Both groups received standard care that was independent of the study. To blind the outcome measure, the research assistant did not explain the reason for the card upon rooming. The provider PA was not informed which patient received the card. Upon discharge, the patient completed a five-question survey regarding the clinic visit.

Interventions

OTHERBiosketch Card

The experimental group received a biosketch card during rooming, pre-clinician encounter that gave an overview of the midlevel providers qualifications.

Sponsors

Desert Orthopedic Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* New Patient * Appointment with a PA

Exclusion criteria

* Non-English Speaker

Design outcomes

Primary

MeasureTime frameDescription
SurveyImmediately following the visitFive question survey following the visit

Contacts

Primary ContactShanthan C Challa
schalla@doclv.com7024998579

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026