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Patient Satisfaction in the Orthopedic Surgery Clinic

NYU Langone Health logo

NYU Langone Health

Status

Withdrawn

Conditions

All

Treatments

Behavioral: Review

Study type

Interventional

Funder types

Other

Identifiers

NCT04343027
20-00152

Details and patient eligibility

About

Patients in the orthopedic surgery clinic routinely fill out a patient- reported outcome measurement survey prior to their visit. These scores are stored in Epic, but are not routinely reviewed with patients during their office visit. Study subjects will be randomly assigned into one of two groups: those who have their patient- reported outcome measurements reviewed with them by their physician, and those who will not have their patient-reported outcome measurements reviewed during the visit. Following the visit, patients will complete a patient satisfaction survey.

Full description

This patient satisfaction survey is a modified version of the Press-Ganey Outpatient Medical Practice 10-question survey. The patient satisfaction survey scores will then be compared between the two groups to quantify the effect of reviewing of patient-reported outcome measurements with patients on their satisfaction with the office visit

Sex

All

Ages

18 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult patients
  • Ages 18 and 100 years
  • Men and women will be included in this study
  • Willing and able to provide consent
  • Able to communicate in English
  • All patients of the Principal Investigator(s) that have an clinic appointment during the study date range will be considered for inclusion in the study

Exclusion criteria

  • Patients whose visit is related to workman's compensation, a disability claim, or a "no-fault" case (i.e. a law suit related to personal injury)
  • Patients that do not complete the patient satisfaction survey following their visit
  • Patient with mental disabilities or other handicap that would interfere with their capability of completing the surveys

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

0 participants in 2 patient groups

Standard of care group
No Intervention group
Description:
Participants who did not have their physicians review their patient-reported outcome measurements with them during the office visit.
Consultation group
Experimental group
Description:
Participants who had their physicians review their patient-reported outcome measurements reviewed with them during the office visit.
Treatment:
Behavioral: Review

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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