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Stability Plus - Outcomes From Extended Continuum of Care

Study the Effects of Pre- and Post-Operative Resistive Exercise in Total Arthroplasty Patients Using the Stability Plus Exercise System

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00756483
Enrollment
200
Registered
2008-09-22
Start date
2008-10-31
Completion date
2009-10-31
Last updated
2008-09-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Arthroplasty

Keywords

Resistance, Exercise

Brief summary

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.

Interventions

None listed

Sponsors

University of Missouri-Columbia
CollaboratorOTHER
Stability Plus, LLC
Lead SponsorINDUSTRY

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

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

Exclusion criteria

* Non-ambulatory patients

Design outcomes

Primary

MeasureTime frame
Pre- and post- study strength assessment tests for joint specific exercises3 months, 6 months and 12 months

Secondary

MeasureTime frame
Reduced recovery time versus current norm3 months, 6 months and 12 months

Countries

United States

Contacts

Primary ContactAnn M Juengermann
JuengermannA@health.missouri.edu
Backup ContactLinda C Landry
LandryL@health.missouri.edu

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026