An Open Label Data Collection Study of My Connect Post-Op, a Post-Operative Communication Tool
Recruiting
Observational Study
Total Hip Replacement
Total Knee Replacement
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 22 – 80
- Sex
- Any
- Study type
- Observational
- Participants needed
- 200 (estimated)
- Sponsor
- Concentra AI, inc · Industry
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
Check Your Eligibility
About This Trial
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 p…
Trial Locations
Loading…
Loading trial locations…
Eligibility Criteria
Inclusion Criteria:
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 Crite…
Contacts
No contact information available.