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Status unknownNCT00756483Updated Sep 22, 2008

Stability Plus - Outcomes From Extended Continuum of Care

An observational study in Arthroplasty, sponsored by Stability Plus, LLC. Status unknown at 1 site in United States. Per ClinicalTrials.gov, last updated 2008-09-22.

Sponsored by Stability Plus, LLC · Observational

The sponsor has not verified this record recently (last verified Sep 2008), so the status shown — last known as Not yet recruiting — may be out of date.
Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
200
Sex
All
01

Study 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.
02

Conditions studied

  • Arthroplasty

Keywords

  • Resistance
  • Exercise
03

In context

Lead sponsor

This is the only study on the registry with Stability Plus, LLC as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

Patients that have undergone total joint replacement - hip or knee

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

Exclusion Criteria:

  • Non-ambulatory patients
05

Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
200 participants (estimated)

Groups and cohorts

  • M, 1

    Male patients that have undergone total knee replacement

  • F, 1

    Female patients that have undergone total knee replacement

  • M, 2

    Male patients that have undergone total hip replacement

  • F, 2

    Female patients that have undergone total hip replacement

06

What researchers measure

Primary outcomes

  1. Pre- and post- study strength assessment tests for joint specific exercises

    Time frame: 3 months, 6 months and 12 months

Secondary outcomes

  1. Reduced recovery time versus current norm

    Time frame: 3 months, 6 months and 12 months

07

Study locations

1 site
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 22, 2008, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00756483
Lead sponsor
Stability Plus, LLC
Collaborators
University of Missouri-Columbia
First posted
Sep 22, 2008
Start date
Oct 2008
Primary completion
Mar 2009 (estimated)
Completion
Oct 2009 (estimated)
Last update
Sep 22, 2008

Study contacts

Ann M Juengermann
Contact
JuengermannA@health.missouri.edu
Linda C Landry
Contact
LandryL@health.missouri.edu
James T Yost
study director · Stability Plus, LLC

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Sep 2008. You cannot join it, but the record below documents what was studied.

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