Gait Retraining to Reduce Knee Osteoarthritis Pain

Sponsor
Stanford University (Other)
Overall Status
Completed
CT.gov ID
NCT01397981
Collaborator
(none)
25
1
1
16.1
1.6

Study Details

Study Description

Brief Summary

The purpose of this study is to determine how well people can be trained to produce new and different movements through the use of haptic feedback. One particular application is retraining individuals to walk differently in order to reduce knee joint loads to prevent or treat knee osteoarthritis as an alternative to surgical treatments.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Gait retraining
Phase 1/Phase 2

Detailed Description

During the movement retraining session, you be given different combinations of haptic, visual, and auditory feedback in order to inform you on desired movement changes. This will take place at the Human Performance Laboratory at Stanford University. Motion analysis will be done while you perform movement activities (such as locomotion).

Prior to performing these movement tasks the investigators will attach reflective markers to your body using tape, pre-wrap and/or ace bandages. The investigators will record motion of your body's movements using infrared cameras which capture anatomical data from the reflective markers on your body.

The investigators will provide you with feedback to inform you of desired movement modifications. Haptic feedback devices such as vibration motors and skin stretch devices will be attached to your body via velcro straps and will be used to give "touch" feedback. There will be a computer monitor in front of you during testing to provide visual feedback. Sounds will be played using speakers near the testing area to provide auditory feedback.

The time needed for set up and performance of the above set of tests is approximately 90 minutes. You will be performing walking and other movements for only a small part of that time. The rest of the time will be spent preparing you for the experiment. After the investigators examine your movement data, if some of the data appear inaccurate or the investigators are unable to process the data, the investigators may ask you to repeat the movement analysis at a later time.

Study Design

Study Type:
Interventional
Actual Enrollment :
25 participants
Allocation:
Non-Randomized
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Evaluation of Haptic Technologies for Movement Retraining
Study Start Date :
Jul 1, 2011
Actual Primary Completion Date :
Apr 1, 2012
Actual Study Completion Date :
Nov 1, 2012

Arms and Interventions

Arm Intervention/Treatment
Experimental: Walking modification

Changing kinematics for walking

Behavioral: Gait retraining
Changing the kinematics of walking

Outcome Measures

Primary Outcome Measures

  1. Measure: Knee pain and function [four weeks]

    Knee pain and function will be assessed through the standardized KOOS survey

Secondary Outcome Measures

  1. Learning retention, knee adduction moment [four weeks]

    Learning retention of gait kinematics and knee joint loading including the knee adduction moment will be measured through motion capture and ground reaction force plates

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Symptoms of medial compartment pain during the previous 6 weeks

  • Radiographic evidence (AP X-ray) of medial compartment knee osteoarthritis (KL score of 3 or less)

  • Ability to walk unaided for 25 minutes without rest

  • Age > 18

Exclusion Criteria:
  • BMI > 30

  • Previous injury or surgery on foot, ankle, knee, hip, or back inhibiting ability to adopt different walking gait

  • Use of shoe insert or hinged knee brace

  • Corticosteroid injection within the previous 6 weeks

  • Age > 80

Contacts and Locations

Locations

Site City State Country Postal Code
1 Stanford University School of Medicine Stanford California United States 94305

Sponsors and Collaborators

  • Stanford University

Investigators

  • Study Director: Pete B Shull, Stanford University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Pete Bradley Shull, Dr., Stanford University
ClinicalTrials.gov Identifier:
NCT01397981
Other Study ID Numbers:
  • SU-07142011-8086
First Posted:
Jul 20, 2011
Last Update Posted:
Mar 6, 2013
Last Verified:
Mar 1, 2013
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 6, 2013