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Clinical Trials/NCT04338425
NCT04338425CompletedNot Applicable

Patient Satisfaction With Postoperative Communication Modality

NYU Langone Health1 site in 1 country295 target enrollmentStarted: December 1, 2018Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
295
Locations
1
Primary Endpoint
Percent of participants' satisfaction with surgeon

Study Overview

Brief Summary

Communication between a surgeon and a patient in the immediate postoperative period is thought to influence patient satisfaction. There is currently no standard of care regarding the optimal form of postoperative communication, nor is there a consensus in our department as to which modality is preferred by patients.The purpose of this study is to determine which form of communication, if any, is preferred by patients. Furthermore, this study aims to evaluate the impact that various forms of communication during the immediate postoperative period have on patient (subject) satisfaction. The study hypothesizes that patient (subject) satisfaction with their surgeon will be highest among those who communicate with their surgeons via videotelephony (i.e., videoconferencing) and that the lowest satisfaction will be among patients (subjects) who did not communicate with their surgeon until their regularly scheduled postoperative office visit. The results of this study may help identify low cost methods for increasing patient satisfaction.

Detailed Description

This is a prospective, randomized study designed to evaluate the effects of different communication modalities between surgeons and patients (subjects) in the immediate postoperative period. Given the nature of the study, it is not possible for either the surgeons or the subjects to be blinded. To reduce bias that may occur due to each surgeon's personal preference for postoperative communication modality, the surgeons (rather than individual subjects) will be randomized to one of the three communication modality groups (no communication on the day of surgery, voice call, or videoconferencing).

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •undergoing surgery at the NYU Langone Orthopedic Center

Exclusion Criteria

  • •Under the age of 18 years old

Arms & Interventions

No Communication group

No Intervention

Participants will not communicate with their surgeons until the post operative office visit.

Voice call group

Active Comparator

Participants will receive voice call from the surgeon after being discharged and before their post operative office visit.

Intervention: Voice call (Behavioral)

Video call group

Active Comparator

Participants will receive video call from surgeon after being discharged and before their post operative office visit

Intervention: Video call (Behavioral)

Outcomes

Primary Outcomes

Percent of participants' satisfaction with surgeon

Time Frame: post operative office visit (1 week after surgery)

The first self reported survey is designed specifically for this study to assess participants' satisfaction with their experience and postoperative communication.

Secondary Outcomes

  • Percent of participants' satisfaction with hospital experience(post operative office visit (1 week after surgery))

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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