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Clinical Trials/NCT01907503
NCT01907503UnknownNot Applicable

Adaptation of Locomotor Activity in Patients Suffering From Hip OA - Analysis of This Adaptation as a Prognostic Criterion for Future Disease Progression

Centre Hospitalier Universitaire Dijon1 site in 1 country200 target enrollmentStarted: February 1, 2008Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Enrollment
200
Locations
1
Primary Endpoint
locomotor activity

Study Overview

Brief Summary

To assess the prognostic value of a characteristic evaluation of gait in persons suffering from hip OA for subsequent indications for THR.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Masking
None

Eligibility Criteria

Ages
45 Years to 75 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Men or women aged between 45 and 75 years Suffering from primary hip osteoarthritis defined according to ACR criteria who presented pain in the hip for at least one month in the preceding 3 months Radiological stage II, III or IV hip OA according to the Kellgren and Lawrence classification Patients able to understand simple instructions des packaging instructions, to give their written informed consent.

Exclusion Criteria

  • Indication for THR at the time of inclusion. Pregnant or breast-feeding women Alzheimer's disease Chronic respiratory insufficiency with clinical manifestations Parkinson's disease Motor neuron disease Major musculo-skeletal disorder (other than hip OA) Severe non-stabilised diabetes Non-stabilised hypertension Hip OA inflammation flare Rapidly-destructive hip OA Radiography to evaluate structural evolution of the disease done more than 12 months previously Presence of OA in another joint, or another osteoarticular or periarticular disease of the lower limbs with, in the opinion of the patient, disability due to this other disease that is greater than the disability caused by the hip OA.
  • Spine disease causing gait disturbance (radiculalgia, lumbar canal stenosis,... with, in the opinion of the patient, disability due to this other disease that is greater than the disability caused by the hip OA.)

Arms & Interventions

Patients with Primary hip osteoarthritis

Other

Patients with Primary hip osteoarthritis

Intervention: Evaluation of the balance of force platform (Procedure)

Healthy volunteer

Other

Healthy volunteer

Intervention: Evaluation of the balance of force platform (Procedure)

Outcomes

Primary Outcomes

locomotor activity

Time Frame: participants will be followed for the duration of hospital stay, an expected average of 2 weeks

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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