Performance in Walking in Osteoarthritis Patients

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-09-19

Study Completion Date

2019-06-17

Brief Summary

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Few data exist to date on the effect of eccentric muscle building in knee osteoarthritis. No studies have compared the effect of eccentric versus concentric reinforcement in knee osteoarthritis. Our study aims to show the effectiveness of an eccentric reinforcement. This is a randomized, interventional trial.

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Detailed Description

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Few data exist to date on the effect of eccentric muscle building in knee osteoarthritis. No studies have compared the effect of eccentric versus concentric reinforcement in knee osteoarthritis. Our study aims to show the effectiveness of an eccentric reinforcement, the interest of a work supervised by a sports coach to maintain activity over time and to study the effect of this activity at the muscular level. The main objective is to study the effect of an eccentric muscle strengthening program on walking performance in osteoarthritis patients. The secondary objectives are to study: the effect of fatigue on walking, the relationship between fatigue and the level of physical activity, the effect of training on perceived fatigue and the effect of training on the function and at muscular level. This is a randomized, interventional trial. 40 subjects are planned. Inclusion criteria include: age 40-85 years, KL 2 and 3. The subjects are divided into two groups to perform either eccentric or concentric work. 2 sessions per week for 6 weeks. At baseline and at the end of the study a clinical evaluation and MRI will be carried out for evaluation of the criteria of judgment

Conditions

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Osteoarthritis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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concentric work

patient suffering from knee osteoarthritis will follow a concentric work. This training is 2 sessions per week for 6 weeks

Group Type ACTIVE_COMPARATOR

concentric work

Intervention Type OTHER

patient will follow 2 concentric trainings per week during 6 weeks

eccentric work

patient suffering from knee osteoarthritis will follow an eccentric work. This training is 2 sessions per week for 6 weeks

Group Type EXPERIMENTAL

eccentric work

Intervention Type OTHER

patient will follow 2 eccentric trainings per week during 6 weeks

Interventions

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eccentric work

patient will follow 2 eccentric trainings per week during 6 weeks

Intervention Type OTHER

concentric work

patient will follow 2 concentric trainings per week during 6 weeks

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Autonomous subjects aged 40 to 85
* Subjects meeting ACR criteria for gonarthrosis
* Subjects with a score of Kellgren and Lawrence at least one knee greater than or equal to 2
* Signature of consent form
* Subjects affiliated to social security

Exclusion Criteria

Subject with a Kellgren and Lawrence stadium at 4 for at least one of his two knees

* Subjects with symptomatic femoro-patellar arthrosis
* Subject with a pathology that makes walking testing impossible.
* Non-autonomous subjects, with a pathology impairing walking
* Subjects with symptomatic osteoarthritis of the hip and / or with a hip or knee prosthesis
* Subject incapable of signing consent and unable to understand information leaflet.

Minimum Eligible Age

40 Years

Maximum Eligible Age

85 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No