Actively Recruiting
An Open Label Data Collection Study of My Connect Post-Op, a Post-Operative Communication Tool
Led by Concentra AI, inc · Updated on 2025-08-15
200
Participants Needed
1
Research Sites
6 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying the use of My Connect Post-Op Software as a communication tool to support recovery after total hip or knee replacement surgery. This open-label, multi-center observational study will evaluate how effectively the software guides patients through their recovery, identifies potential complications, and provides recommendations based on structured conversations. The study includes adult orthopedic patients undergoing elective joint replacement surgeries who meet eligibility requirements. Participants will be trained on using the My Connect Post-Op device before their surgery during an in-office visit. After discharge, they will engage with the software daily for 30 days, responding to prompts and questions about their recovery. The software collects data on pain, sleep, activity, medication use, and diet, using tools like the GRASP device and smartphone slider for pain reporting. A control group will be formed by reviewing records of past patients who underwent similar surgeries. The study also includes a provider dashboard for managing patients and conducting real-time chats. During the 30-day study period, researchers will collect detailed conversation logs and monitor how the software supports clinical decision-making. Patient and provider satisfaction will be assessed periodically. Data on the software's chat responsiveness, clarity, and usability will also be gathered. The study aims to ensure the communication tool covers a wide range of clinical scenarios and supports patient recovery effectively.
CONDITIONS
Brief Title
An Open Label Data Collection Study of My Connect Post-Op, a Post-Operative Communication Tool
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Orthopedic patients scheduled for elective single or double knee or hip replacement surgery
- Age between 22 and 80 years
- Owns a smartphone
- Speaks and understands written and spoken English
- Able to give written informed consent
You will not qualify if you...
- Known diagnosis of a psychiatric disorder
- Known opioid dependence that may complicate participation
- Participation in another clinical trial involving a drug, device, or medical procedure within 30 days before or during this trial
- Any condition that may complicate or prevent participation, such as physical impairment or noncooperation as judged by the investigator
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person) for training and study requirements discussion before surgery
Duration - Approximately 30 days
Participants undergo orthopedic total hip or knee replacement surgery and start using the My Connect Post-Op communication tool after discharge.
Daily engagement with the software throughout the 30-day post-op period
Duration - Up to 30 days post-surgery
Participants' interactions with the communication tool are logged, and patient and provider satisfaction data are collected periodically during recovery.
Periodic assessments through the software during the 30-day study period
Trial Site Locations
Total: 1 location
1
Kansas Joint and Spine
Wichita, Kansas, United States, 67226
Actively Recruiting
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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