A Rehabilitation Tool to Determine Patient's Stay in Hospital After Joint Replacement

Total Joint Replacement Surgery Clinical Trial

Official title:

A Rehabilitation Tool to Determine Patient's Stay in Hospital After Joint Replacement

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT03776357
• Other study ID #: 46061
• Status: Terminated
• Phase: N/A
• Start date: August 26, 2019
• Est. completion date: March 10, 2020

Study information

• Verified date: June 2022
• Source: Stanford University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is the research study of a rehabilitation tool that informs, guides and empowers clinicians to care for their patients. We hope to learn ways to improve patient outcomes, reduce costs and increase value to the healthcare system

Description:

The investigator hope to learn co-relation between the rehab tool and clinical findings and analyse association if any. Rehab tool will optimize care according to the patient's specific needs and provided insights to patients length of stay in the hospital. these data driven insights will be used to observe correlation between machine and clinic data

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 9
• Est. completion date: March 10, 2020
• Est. primary completion date: March 10, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 99 Years

Eligibility

Inclusion Criteria:

• Patient scheduled for Primary unilateral total joint replacement

• Patient age should be more than or equal to 18 years.

• Patient must speak English

Exclusion Criteria:

• Patients undergoing bilateral primary knee replacement surgery

• Patients undergoing revision knee replacement surgery

• No uncorrectable deformity

• No deformity greater than 15 degree

• No hip arthritis

• No wheelchair dependency

• Patients not willing and capable to sign the written informed consent

Related Conditions & MeSH terms

• Total Joint Replacement Surgery

Intervention

Device:
• VERA clinic
A software system used with the Microsoft Kinect intended to support the physical rehabilitation of adults in the clinic and at home.

Locations

Country	Name	City	State
United States	Stanford outpatient center	Redwood City	California

Sponsors (1)

Lead Sponsor	Collaborator
Derek Amanatullah

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Length of Stay in Hospital Through Discharge		Up to 2 days
Secondary	Number of Participants Requiring Gait Aid Use	The gait aide use ranges in the order of decreasing performance as Nothing > Cane > crutch > walker.	3 months post operative visit
Secondary	Knee Society Score (KSS)	To assess the effectiveness of the device by calculating knee society score (KSS) after surgery. The scale ranges from 0-100 with grading as Score 80-100 - Excellent Score 70-79 - Good Score 60-69 - Fair Score below 60 - Poor	3 months post operative visit
Secondary	Knee Range of Motion	To assess the effectiveness of the device by calculating range of motion (maximum degrees)	3 months post operative visit