NCT00756483

Brief Summary

Basic Protocol

  • 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
  • Perform Initial Assessment using Basic Exercises for the Surgical Procedure
  • Enter Assessment Data at www.stabilityplus.net (through the LOGIN tab/Portal)
  • Within portal, modify Basic Exercise Program to create customized Stability Plus prescription for the patient
  • Monitor patient progress through Stability Plus portal.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
200

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Oct 2008

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

September 18, 2008

Completed
4 days until next milestone

First Posted

Study publicly available on registry

September 22, 2008

Completed
9 days until next milestone

Study Start

First participant enrolled

October 1, 2008

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2009

Completed
7 months until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2009

Completed
Last Updated

September 22, 2008

Status Verified

September 1, 2008

Enrollment Period

5 months

First QC Date

September 18, 2008

Last Update Submit

September 19, 2008

Conditions

Arthroplasty

Keywords

ResistanceExercise

Outcome Measures

Primary Outcomes (1)

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

    3 months, 6 months and 12 months

Secondary Outcomes (1)

  • Reduced recovery time versus current norm

    3 months, 6 months and 12 months

Study Arms (4)

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

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Patients that have undergone total joint replacement - hip or knee

You may qualify if:

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

You may not qualify if:

  • Non-ambulatory patients

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Missouri Hospital

Columbia, Missouri, 65212, United States

Location

MeSH Terms

Conditions

Motor Activity

Condition Hierarchy (Ancestors)

Behavior

Study Officials

  • James T Yost

    Stability Plus, LLC

    STUDY DIRECTOR

Central Study Contacts

Ann M Juengermann

CONTACT

JuengermannA@health.missouri.edu

Linda C Landry

CONTACT

LandryL@health.missouri.edu

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
PROSPECTIVE
Sponsor Type
INDUSTRY

Study Record Dates

First Submitted

September 18, 2008

First Posted

September 22, 2008

Study Start

October 1, 2008

Primary Completion

March 1, 2009

Study Completion

October 1, 2009

Last Updated

September 22, 2008

Record last verified: 2008-09

Locations

US(1)