Stability Plus - Outcomes From Extended Continuum of Care

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

200 participants

Study Classification

OBSERVATIONAL

Study Start Date

2008-10-31

Study Completion Date

2009-10-31

Brief Summary

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Basic Protocol

1. Identify participant(s)
2. Request patient participation/Acquire Consent
3. Register patient at www.stabilityplus.net through the LOGIN tab

* Patient ID (Name/Initials/SSN or any combination thereof)
* Gender
* Age
* Surgical Procedure
* Date of Surgery
* Select Basic Exercise Program that corresponds with Surgical Procedure
4. Perform Initial Assessment using Basic Exercises for the Surgical Procedure
5. Enter Assessment Data at www.stabilityplus.net (through the LOGIN tab/Portal)
6. Within portal, modify Basic Exercise Program to create customized Stability Plus prescription for the patient
7. Monitor patient progress through Stability Plus portal.

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Detailed Description

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Conditions

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Arthroplasty

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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M, 1

Male patients that have undergone total knee replacement

No interventions assigned to this group

F, 1

Female patients that have undergone total knee replacement

No interventions assigned to this group

M, 2

Male patients that have undergone total hip replacement

No interventions assigned to this group

F, 2

Female patients that have undergone total hip replacement

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Undergone total joint replacement
* Must be able to complete pre-operative strength assessment
* Must be able to exercise using specified resistive bands