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

NCT ID: NCT03776357

Last Updated: 2022-06-30

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

TERMINATED

Clinical Phase

NA

Total Enrollment

9 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-08-26

Study Completion Date

2020-03-10

Brief Summary

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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

Detailed Description

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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

Conditions

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Total Joint Replacement Surgery

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

NONE

Study Groups

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Experimental

The application used is build upon the company's category-defining, FDA- cleared Virtual Exercise Rehabilitation Assistant (VERA™) and create a platform that streamlines the performance and management of post-acute care physical therapy. The rehab tool will provide us with functional outcome score.

Group Type EXPERIMENTAL

VERA clinic

Intervention Type DEVICE

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

Interventions

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VERA clinic

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

Intervention Type DEVICE

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

99 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Derek Amanatullah

OTHER

Sponsor Role lead

Responsible Party

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Derek Amanatullah

Assistant professor

Responsibility Role SPONSOR_INVESTIGATOR

Locations

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Stanford outpatient center

Redwood City, California, United States

Site Status

Countries

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United States

Provided Documents

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Document Type: Study Protocol

View Document

Other Identifiers

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46061

Identifier Type: -

Identifier Source: org_study_id

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