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NCT03443284

Health Partner Evaluation at Providence

Terminated NA Last updated 2 January 2020
What this trial tests

NA trial testing Health Partner in Total Knee Arthroplasty; Total Hip Arthroplasty in 79 participants. Terminated before completion.

Timeline
11 December 2018
Primary endpoint
17 December 2019
17 December 2019

Quick facts

Lead sponsorDePuy Orthopaedics
PhaseNA
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposesupportive care
Enrollment79
Start date11 December 2018
Primary completion17 December 2019
Estimated completion17 December 2019
Sites3 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

DePuy Orthopaedics — full company profile →

Who can join

18 and older, any sex, with Total Knee Arthroplasty; Total Hip Arthroplasty. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Health Partner

Trials testing the same drug.

Other DePuy Orthopaedics trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03443284.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing