Patient Satisfaction in the Orthopedic Surgery Clinic

NCT ID: NCT04343027

Last Updated: 2022-12-06

Basic Information

• Recruitment Status: WITHDRAWN
• Clinical Phase: NA
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-08-31
• Study Completion Date: 2023-06-30

Brief Summary

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.

Detailed 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

Conditions

All

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: OTHER
• Blinding Strategy: SINGLE

Study Groups

Standard of care group

Participants who did not have their physicians review their patient-reported outcome measurements with them during the office visit.

Group Type: NO_INTERVENTION

No interventions assigned to this group

Consultation group

Participants who had their physicians review their patient-reported outcome measurements reviewed with them during the office visit.

Group Type: EXPERIMENTAL

Review

Intervention Type: BEHAVIORAL

Physicians will review patient-reported outcome measurements with their patients during office visits.

Interventions

Review

Physicians will review patient-reported outcome measurements with their patients during office visits.

Intervention Type: BEHAVIORAL

Eligibility Criteria

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

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 100 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

NYU Langone Health

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Andrew Rokito, MD

Role: PRINCIPAL_INVESTIGATOR

NYU Langone Health

Other Identifiers

20-00152

Identifier Type: -

Identifier Source: org_study_id