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Gait Retraining for Runners With Knee Osteoarthritis

The Effects of Gait Retraining in Runners With Knee Osteoarthritis

Status
Withdrawn
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03314428
Enrollment
0
Registered
2017-10-19
Start date
2025-07-01
Completion date
2026-07-01
Last updated
2026-03-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Osteoarthritis, Knee

Brief summary

Tibiofemoral osteoarthritis (TFOA) is highly prevalent in older adults, and often causes symptoms and functional limitations. Physical activity is widely advocated in people with TFOA, and running is an easy and accessible activity that provides many benefits on general health. However, running induces high knee loads, which could potentially contribute to symptoms of runners with TFOA. Previous studies have suggested that running gait modifications can help in decreasing symptoms and knee loading in runners with knee conditions. Yet, no study has been conducted in runners with TFOA. This intervention study will investigate the effects of a 4-week running gait retraining program on symptoms and running biomechanics in runners with TFOA. We hypothesize that running modifications will decrease symptoms, improve function and reduce knee loading.

Interventions

BEHAVIORALGait retraining

Over a 4-week period, runners will be asked to increase their step rate to reduce knee loading during running. Specifically, they will have to increase their preferred step rate by 10% during weekly laboratory running sessions as well as during habitual running training. In the laboratory, runners will be provided with live visual/auditory biofeedback on step rate and asked to target a specific value representing 110% or preferred step rate. During their individual running sessions, runners will be wearing a GPS-enabled watch that will provide feedback on live step rate, and they will be asked to maintain the same value as in the laboratory.

Sponsors

University of British Columbia
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Masking description

Data will be analyzed by an assessor blinded to date of data collection for each testing session. Following data collection, a researcher not involved with data collection or analysis will re-code data timepoints to ensure that the assessor is unaware of the timepoint each datapoint was obtained.

Intervention model description

Single Group cohort study

Eligibility

Sex/Gender
FEMALE
Age
40 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* TFOA of Grade 2 (mild) or 3 (moderate) on the Kellgren and Lawrence scale * report knee pain greater than or equal to 3/10 on a numerical pain rating scale (0-10) during most days of the previous month * run at least 10 km per week for a minimum of 6 months * declare being comfortable running on a treadmill for at least 30 minutes

Exclusion criteria

* history of traumatic knee injury * neurological or inflammatory arthritic condition * cardiovascular or cardiopulmonary disease preventing from safely performing moderate intensity running * presence of any lower limb condition affecting running (other than TFOA) * use of any oral or injected corticosteroids or viscosupplementation in the previous six months * regular use of non-steroidal anti-inflammatory drugs, analgesics or knee unloading bracing devices before, during or after running * non-English speaking

Design outcomes

Primary

MeasureTime frameDescription
Knee Osteoarthritis Outcome Score (KOOS) changeBaseline, 2 weeks, 4 weeks, 2 months, 3 months, 4 monthsValidated questionnaire on symptoms and functional limitations related to knee osteoarthritis. The score is expressed in percentage (0-100), with 0 representing extreme knee problems and 100 representing no knee problems.
Peak knee adduction moment impulse changeBaseline, 4 weeks, 4 monthsValidated surrogate measure of knee joint loading during movement. Expressed as Nm/kg\*sec

Secondary

MeasureTime frameDescription
Numerical pain rating scale for pain during running changeBaseline, 2 weeks, 4 weeks, 2 months, 3 months, 4 monthsValidated scale ranging from 0 (no pain) to 10 (worst imaginable pain), in which participants rate their worst level of pain during running over the previous week.
Step rate changeBaseline, 4 weeks, 4 monthsNumber of steps taken during one minute of running.
Peak knee flexion moment impulse changeBaseline, 4 weeks, 4 monthsValidated surrogate measure of knee joint loading during running. Expressed as Nm/kg\*sec

Countries

Canada

Contacts

PRINCIPAL_INVESTIGATORMichael A Hunt, PT, PhD

University of British Columbia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026