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Efficacy of Eccentric Resistance Training in Persons With Knee Osteoarthritis

Efficacy of Eccentric Resistance Training in Persons With Knee Osteoarthritis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02350387
Enrollment
32
Registered
2015-01-29
Start date
2015-01-31
Completion date
2015-12-31
Last updated
2016-02-26

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

Conditions

Osteoarthritis

Brief summary

The purpose of this study is to determine if there are differences in balance, strength, functional performance and self-reported outcomes for subjects with knee osteoarthritis who complete a low intensity, long duration eccentric training program compared to those who complete a high intensity, short duration eccentric training program. This study will be utilizing the Eccentron (manufactured by BTE Technologies) for the performance of all eccentric exercise.

Detailed description

Arthritis is the leading cause of disability in the United States. Osteoarthritis (OA) is the most common type of arthritis and affects nearly 27 million Americans. Knee OA is the most common type of osteoarthritis and is estimated to affect 42.1% of women and 31.2% of men over the age of 60. Osteoarthritis is most likely multi-factorial with several underlying causes. It is no longer considered a degenerative joint disease but rather a process that involves dynamic biomechanical, biochemical, and cellular processes. It not only involves degeneration of the articular cartilage, but also inflammation of the synovium, changes to the underlying subchondral bone, and the development of osteophytes. Currently, it appears that numerous systemic factors can lead to the initiation of OA through different causal pathways . These systemic causes can then be amplified by local factors such as trauma or increased loading caused by obesity. Currently, there is no cure for OA and attempts to find a disease modifying drug have been unsuccessful. Thus, treatment currently focuses on mitigating factors that are known to affect the radiographic progression of the disease as well as lead to activity limitation and participation restriction.9,10 Decreases in lower extremity strength are a major cause of activity limitations given the vital role of strength in activities of daily living. One method that is used to mitigate progressing factors is through the use of an exercise program. Many types of exercise have been used successfully in the literature including resistance training. Resistance training can take many different forms such as isometric, isotonic (concentric and/or eccentric) or isokinetic with various intensities. Presently, there is little evidence for the use of eccentric training interventions for patients with knee OA. This study aims to further examine this type of resistance training for the OA population. Therefore, the purpose of this study is to examine the effects of low intensity, long duration eccentric resistance training and high intensity, short duration eccentric resistance training in individuals with knee OA. Ideally, this study will allow us to determine the overall effects of eccentric resistance training as well as the potential differences of the two types of eccentric resistance training.

Interventions

PROCEDUREHigh Intensity Short Duration Exercise

Participants randomized to this group will perform 4 sets of 8-15 repetitions of eccentric exercise using the Eccentron set at 50-80% of the participant's one repetition maximum.

PROCEDURELow intensity Long Duration Exercise

Participants randomized to this group will perform 5-20 minutes of continuous eccentric exercise using the Eccentron set at 50% of the participant's one repetition maximum.

Sponsors

Regis University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
55 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Individuals will be included in the study if they are: * at least 55 years old, * cognitively able to understand directions, * able to ambulate at least 50 feet without stopping, * are currently experiencing knee pain and * meet at least 3 out of 6 criteria of the European League Against Rheumatism (EULAR) criteria for knee osteoarthritis diagnosis.

Exclusion criteria

Individuals will be excluded from the study if they have: * a diagnosed medical condition that would limit physical ability, including acute or active fractures, myocardial infarctions, stroke, * a traumatic brain injury within the last 6 months, or * joint replacement within the last 12 months. Individuals with chronic neurological disorders limiting motion or present with any known contraindication for balance training will also be excluded from the study.

Design outcomes

Primary

MeasureTime frameDescription
Isometric quadriceps strength as measured by a hand held dynamometerChange from baseline to 8 weeksThe primary outcome for this study is the change in quadriceps strength from baseline to 8 weeks (end of intervention) in both experimental groups.

Secondary

MeasureTime frameDescription
Timed Up and Go TestChange from baseline to 8 weeks
6-minute Walk TestChange from baseline to 8 weeks
Five times sit to stand testChange from baseline to 8 weeks
Lower extremity muscle strength as measured by a hand held dynamometerChange from baseline to 8 weeksTrunk flexion/extension, Hip Abduction/Extension, Knee Flexion/Extension, and Ankle Plantarflexion and Dorsiflexion will be assessed at baseline and 8 weeks by a hand held dynamometer.
Arthritis Impact Measurement Scale (AIMS)Change from baseline to 8 weeks
Pain and muscle soreness ( assessed utilizing a numeric pain rating scale)At the beginning of every treatment session and following every treatment session for the 8 week interventionPain and muscle soreness will be assessed utilizing a numeric pain rating scale at the beginning and end of every treatment session.
Balance (assessed utilizing the romberg, sharpened romberg, one-legged stance test, functional reach test, and step test)Change from baseline to 8 weeksBalance will be assessed utilizing the romberg, sharpened romberg, one-legged stance test, functional reach test, and step test.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026