Cycling Intervention on Symptoms of Patients With Knee Osteoarthritis

This study is designed to determine the effect of a cycling training program which modulates frontal and sagittal plane knee joint loading with graded increases of Q-Factor and cycling workrate in persons with symptomatic knee osteoarthritis.

Study Overview

• Status: Unknown
• Conditions: Osteoarthritis, Knee
• Intervention / Treatment: Procedure: Q-Factor Intervention

Detailed Description

The knee joint is one of the most common joints affected by osteoarthritis, and knee osteoarthritis is primarily observed in the medial compartment. This is in part attributable to the increased load experienced by the medial compartment during level walking. Patients with symptomatic knee osteoarthritis exhibit altered gait mechanics; namely a reduced loading response knee extension moment and an increased internal knee abduction moment. As a surrogate measure for medial compartment joint loading, loading response knee abduction moment in level walking has been shown to increase with the severity of knee osteoarthritis.

Recent gait modification research has shown that increased step-width decreases peak Knee abduction moment for persons with knee osteoarthritis. The inter-pedal width of a bicycle or cycle ergometer, known as Q-Factor, is analogous in cycling to step-width in gait. In contrast to gait, increased Q-Factor has been shown to increase the knee abduction moment during stationary cycling. Modulating sagittal and frontal plane loading of the knee in a graded manner during cycling may promote healthy adaptation to muscle weakness and pain. This adaptation may be manifest through restoration of altered knee joint biomechanics (knee extension moment, knee abduction moment), which, in turn, may also provide benefit to gait mechanics.

• Study Type: Interventional
• Enrollment (Anticipated): 30
• Phase: Not Applicable

Contacts and Locations

Study Locations

• United States
  • Tennessee
    • Knoxville, Tennessee, United States, 37996
      • Recruiting
      • Biomechanics/Sports Medicine Lab
      • Contact: Songning Zhang, PhD; Phone Number: 865-974-4716; Email: szhang@utk.edu
      • Contact: Tanner ThorsenZhang, MS; Phone Number: 865-974-2091; Email: tthorsen@vols.utk.edu
      • Principal Investigator: Tanner Thorsen, MS
      • Principal Investigator: Songning Zhang, PhD

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 46 years to 71 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Men and Women between the ages of 50 and 75 years old.
• Diagnosed with medial compartment tibiofemoral osteoarthritis in one of their knees.
• Be able to walk unaided for at least 25 consecutive minutes.
• Present with knee pain for at least 6 months occurring on a majority of the days in the month, or on most days (more than or equal to 4 of 7 days in a week) in one or both knees for at least 4 months.
• Osteophytes on knee x-rays.
• Grade 2 or higher out of a maximum of 4 on a modified Kellgren/Lawrence grade on the knee radiograph.

Exclusion Criteria:

• Initial Visual Analog Scale pain scores greater than 7.
• Diagnosed osteoarthritis of ankles, hips, or symptomatic osteoarthritis of the spine.
• Arthroplasty of any other lower extremity joint.
• BMI value greater than 40 kg/m2.
• Any major lower extremity injury in the past 6 months.
• Systemic Inflammatory Arthritis.
• Systemic Pain Conditions.
• Neurological Conditions that impact gait or cycling.
• Pregnant or Nursing Women.
• Major cardiovascular disease with an exercise limitation prescribed by a physician.
• Steroid injection at the knee within the previous 3 months.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm

Intervention / Treatment

Experimental: Q-Factor Intervention; Participants will progress through three increasing Q-Factors for each cycling workrate; Q-Factor 1 (Q1, 192mm), Q2 (234mm), Q3 (276mm). After completing bouts of all three Q-Factors for a given workrate, workrate will be increased by 20 Watts and bouts at each Q-Factor will be repeated.

Procedure: Q-Factor Intervention; The intervention period will consist of 12 training sessions across four consecutive weeks, with three training sessions held per week. If pain is not increased or reduced and Rating of Perceived Exertion is ≤12, the participant will progress to the next bout. If pain is increased from the pre-bout pain score, participants will repeat the bout, at the same workrate and Q-Factor settings. Following this fashion, participants will progress through three increasing Q-Factors for each given workrate; Q-Factor 1 (Q1, 192mm), Q2 (234mm), Q3 (276mm). After completing bouts of all three Q-Factors for a given workrate, workrate will be increased by 20 Watts and bouts at each Q-Factor will be repeated. For each training session, participants will complete bouts of cycling until 1) the maximum number of bouts (4 bouts) has been accomplished, 2) self-reported Rating of Perceived Exertion >12, indicating a transition to moderate physical activity, or 3) self-reported pain >5.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Knee Abduction Moment - Cycling	Change in Knee Extension Moment during cycling.	Baseline, 1 month, 2 month
Knee Abduction Moment - Gait	Change in Knee Extension Moment during gait.	Baseline, 1 month, 2 month

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Visual Analog Pain	Self-Reported pain intensity during gait and cycling reported on a scale from 1-10 with higher scores reflecting more pain.	Immediately following exercise (walking and cycling).
Knee Extension Moment - Cycling	Change in Knee Extension Moment during cycling	Baseline, 1 month, 2 month
Knee Extension Moment - Gait	Change in Knee Extension Moment during Gait	Baseline, 1 month, 2 month
Knee Injury and Osteoarthritis Outcome Score	Change in Knee Injury and Osteoarthritis Outcome Score reported on a scale from 0 to 100, with 0 representing extreme problems and 100 representing no problems.	Baseline, 1 month, 2 month

Collaborators and Investigators

• Sponsor: The University of Tennessee, Knoxville
• Investigators: Principal Investigator: Tanner Thorsen, MS, University of Tennessee, Knoxville

Study record dates

Study Major Dates

• Study Start (Actual): December 17, 2019
• Primary Completion (Anticipated): May 31, 2021
• Study Completion (Anticipated): May 31, 2021

Study Registration Dates

• First Submitted: October 22, 2019
• First Submitted That Met QC Criteria: October 23, 2019
• First Posted (Actual): October 25, 2019

Study Record Updates

• Last Update Posted (Actual): April 7, 2020
• Last Update Submitted That Met QC Criteria: April 6, 2020
• Last Verified: April 1, 2020

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Joint Diseases; Musculoskeletal Diseases; Rheumatic Diseases; Arthritis; Osteoarthritis; Osteoarthritis, Knee
• Other Study ID Numbers: UTK IRB-19-05254-XP

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: No

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No