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Clinical Trials/NCT03167502
NCT03167502CompletedNot Applicable

Performance in Walking in Osteoarthritis Patients: the Role of Fatigue and the Effect of an Eccentric Muscle Building Program

Centre Hospitalier Universitaire de Nice1 site in 1 country40 target enrollmentStarted: September 19, 2017Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
40
Locations
1
Primary Endpoint
Walking performance

Study Overview

Brief Summary

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.

Detailed Description

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

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
40 Years to 85 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

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.

Arms & Interventions

concentric work

Active Comparator

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

Intervention: concentric work (Other)

eccentric work

Experimental

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

Intervention: eccentric work (Other)

Outcomes

Primary Outcomes

Walking performance

Time Frame: after 6 training weeks

6-minute walk test

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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