An Open Label Data Collection Study of My Connect Post-Op, a Post-Operative Communication Tool
Eligible age
22–80 yrs
Accepts
All genders
Locations
1 state
Healthy volunteers
No
See if you qualify for this study
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About this study
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.
Sponsor: Concentra AI, inc
You may qualify if…
- ✓ 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 may not qualify if…
- ✕ 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
Where it's recruiting
Wichita
Source: ClinicalTrials.gov · NCT07120191 · last updated 2025-08-15