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Clinical Trials/NCT03776357
NCT03776357TerminatedNot Applicable

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

Derek Amanatullah2 sites in 1 country9 target enrollmentStarted: August 26, 2019Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Terminated
Sponsor
Enrollment
9
Locations
2
Primary Endpoint
Length of Stay in Hospital Through Discharge
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief 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

Detailed 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

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Health Services Research
Masking
None

Eligibility Criteria

Ages
18 Years to 99 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

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

Outcomes

Primary Outcomes

Length of Stay in Hospital Through Discharge

Time Frame: Up to 2 days

Secondary Outcomes

  • Knee Society Score (KSS)(3 months post operative visit)
  • Knee Range of Motion(3 months post operative visit)
  • Number of Participants Requiring Gait Aid Use(3 months post operative visit)

Investigators

Sponsor
Derek Amanatullah
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Derek Amanatullah

Assistant professor

Stanford University

Study Sites (2)

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