A Personalized Medicine Prehabilitation Intervention Delivered Using Wearable Mobile Devices to Improve Cognitive Function in Elective Joint Replacement Surgery
Sponsor: University of Pennsylvania
Trial Details
| Condition | Arthropathy of Knee Joint, Arthropathy of Hip Joint |
| Intervention | personalized prehabilitation |
| Phase | NA |
| Status | Suspended |
| Participants | 28 |
| Est. Completion | 31 Dec 2028 |
| Last Updated | 29 May 2026 |
Primary Outcome
Change from baseline, pre-prehabilitation cognitive function at 30±2 days post-operative
Eligibility Criteria
Inclusion Criteria
Inclusion Criteria: * Adults scheduled for elective arthroplasty; * ≥55 years of age; * Capable of giving informed consent; * Willing to comply either to undergo prehabilitation (cases) or standard preoperative care (control); * Own a smartphone. Exclusion Criteria: * Patients with bilateral or revision surgeries; * Diagnosis of pre-existing dementia; * Test result of \<20 in the MoCA indicating moderate to severe dementia; * Diagnosis of acute stroke; * Diagnosis of neurologic injury; * Current alcohol (more than 2 drinks a day with last drink within the past 3 days) or substance abuse (positive urine dip test for illicit drugs) history at risk of postoperative withdrawal; * Active diagnosis of alcohol or substance abuse; * Recent travel across more than two (2) time zones (within the past month); * Planned travel across more than two (2) time zones during the planned study activities; * Subjects, who have received an experimental drug, used an experimental medical device within 30 days prior to screening, or who gave a blood donation of ≥ one pint within 8 weeks prior to screening; * Subjects without access to WiFi in their or close to home or at work.
Trial Sites
Countries
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