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
30 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official 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 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
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 procedure within 30 days before or during this trial
- Any condition that may complicate or prevent participation, such as physical impairment or noncooperation as determined by the Investigator
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
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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