Stability Plus - Outcomes From Extended Continuum of Care
Public ClinicalTrials.gov record NCT00756483. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
Study the Effects of Pre- and Post-Operative Resistive Exercise in Total Arthroplasty Patients Using the Stability Plus Exercise System
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
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.
Study identification
- NCT ID
- NCT00756483
- Recruitment status
- Not listed
- Study type
- Observational
- Phase
- Not listed
- Enrollment
- 200 participants
Conditions and interventions
Conditions
Interventions
Not listed
Eligibility (public fields only)
- Age range
- Not listed
- Sex
- All
- Healthy volunteers
- Accepts healthy volunteers
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Sep 30, 2008
- Primary completion
- Feb 28, 2009
- Completion
- Sep 30, 2009
- Last update posted
- Sep 21, 2008
2008 – 2009
United States locations
- U.S. sites
- 1
- U.S. states
- 1
- U.S. cities
- 1
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| University of Missouri Hospital | Columbia | Missouri | 65212 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT00756483, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Sep 21, 2008 · Synced Sep 4, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT00756483 live on ClinicalTrials.gov.