RECRUITING

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

Description

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.

Study Overview

Study Details

Study overview

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.

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

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

Condition
This Study Will Collect Data Related to the Use of an AI Assisted Post op Communication Tool
Intervention / Treatment

-

Contacts and Locations

Wichita

Kansas Joint and Spine, Wichita, Kansas, United States, 67226

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * 1) Known diagnosis of a psychiatric disorder. 2) Known opioid dependence in the Investigator's opinion that may complicate participation.

Ages Eligible for Study

22 Years to 80 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Concentra AI, inc,

Study Record Dates

2025-11-30