RecruitingNCT07120191

An Open Label Data Collection Study of My Connect Post-Op, a Post-Operative Communication Tool

Sponsor

Concentra AI, inc

Enrollment

200 participants

Start Date

May 1, 2025

Study Type

OBSERVATIONAL

Conditions

Total Knee Replacement total hip replacement

Summary

This open label, multi-center study will collect data from the participant's use of My Connect Post-Op Software as a post-operative communication solution in supporting patient recovery through Technology-Assisted Conversation (TAC). The application will be tested by patients who have undergone total joint replacement as a post-op communication tool. Data will be collected on how effectively the product guides patients through their recovery, identifying potential complications, and providing appropriate recommendations based on structured question pairs.

Eligibility

Min Age: 22 YearsMax Age: 80 Years

Inclusion Criteria2

Orthopedic patients scheduled for elective joint arthroplasty (single or double knee, or single or double hip replacement surgery).
Age 22-80 years. Owns a smart phone. Speaks and understands written and spoken English. Ability to give written informed consent.

Exclusion Criteria3

Known diagnosis of a psychiatric disorder. Known opioid dependence in the Investigator's opinion that may complicate participation.
Participation in another clinical trial investigating a drug, medical device, or a medical procedure in the 30 days preceding trial inclusion and throughout the duration of the trial.
Any condition that in the Investigator's opinion may complicate or preclude the subject from participating in this trial, such as physical impairment or noncooperation

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Interventions

DEVICEpost op communication software

MyConnect Post Op is a communication tool that utilizes Technology Assisted Conversation to aid in the recovery of total knee and hip replacement patients