Actively Recruiting
Virtual Rehabilitation Platform for Patients With Knee Prothesis
Led by Trak Health Solutions S.L. · Updated on 2024-12-06
20
Participants Needed
1
Research Sites
56 weeks
Total Duration
On this page
Sponsors
T
Trak Health Solutions S.L.
Lead Sponsor
B
Biobizkaia Health Research Institute
Collaborating Sponsor
AI-Summary
What this Trial Is About
This clinical trial aims to evaluate the effectiveness and usability of the Trak Rehabilitation Platform in patients who have undergone knee replacement surgery. Its main questions are whether the Trak platform combined with conventional therapy helps patients achieve optimal functionality with fewer in-person sessions compared to conventional rehabilitation alone and whether the Trak platform improves adherence to treatment, independence in daily activities, and quality of life while reducing resource consumption. Researchers will compare the use of the Trak platform combined with conventional rehabilitation to standard rehabilitation practices to determine its impact on functional outcomes, patient and provider satisfaction, and resource efficiency. Participants will: * Use the Trak Platform as part of their personalized treatment plan. * Attend face-to-face rehabilitation sessions as prescribed. * Participate in assessments to measure functionality, adherence, independence, quality of life, and resource utilization.
CONDITIONS
Official Title
Virtual Rehabilitation Platform for Patients With Knee Prothesis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged over 18 and up to 85 years
- Patients who underwent knee prosthesis surgery at the Knee Unit of Cruces University Hospital
- Patients needing on-site rehabilitation at Cruces University Hospital rehabilitation service
- Patients who have signed the Informed Consent
You will not qualify if you...
- Patients with intellectual disability or cognitive impairment
- Patients with a history of knee infection
- Patients unable to use mobile apps, phones, tablets, or computers without family or caregiver support
- Patients who have not signed the Informed Consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Cruces University Hospital (HU Cruces, OSI EEC)
Barakaldo, Basque Country, Spain, 20018
Actively Recruiting
Research Team
J
JUAN F DUARTE MENDOZA
CONTACT
R
RAÚL ZABALLA FERNÁNDEZ
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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