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Clinical Trial Summary

This is a prospective, mixed methods, multi-center, randomized, comparative, controlled study. Providence Health & Services will enroll a total of 296 subjects (18 years or older) who are electing to have total knee or hip replacement surgery. Subjects will be randomized to either the treatment group (Health Partner alongside standard care) or the control group (standard care alone). Health Partner is a combination of an iPhone or iPod Touch Operating System mobile application and a health care provider portal. The primary objective is to compare care plan adherence (pre- and post-surgery) for Health Partner vs. control subjects. Secondary objectives include evaluating all-cause medical resource utilization, communication with health care provider, well-being, fear of surgery, confidence in recovery from surgery, sleep, and patient satisfaction for 90 days post-surgery. To evaluate the behavioral factors associated with care path adherence using a qualitative interview method.To evaluate the usability and preferences of patients in their interaction with the intervention using a qualitative interview method, for product development.

The total planned study duration is approximately 1 year and 7 months.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Total Knee Arthroplasty; Total Hip Arthroplasty

NCT number NCT03443284
Study type Interventional
Source DePuy Orthopaedics
Contact
Status Terminated
Phase N/A
Start date December 11, 2018
Completion date December 17, 2019

See also
  Status Clinical Trial Phase
Terminated NCT03386786 - Health Partner Evaluation at Princeton N/A