Actively Recruiting

Age: 22Years - 80Years
All Genders
NCT07120191

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

Age: 22Years - 80Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Trial Site Locations

Total: 1 location

1

Kansas Joint and Spine

Wichita, Kansas, United States, 67226

Actively Recruiting

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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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