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Prevalence,Natural History,Prognosis Factor,QualityofLife,Health Care Consumption and Social Consequences of Symptomatic Knee and Hip Osteoarthritis in France

Knee and Hip OsteoArthritis Long Term Assessment. Prevalence, Natural History, Prognosis Factor, Quality of Life, Health Care Consumption and Social Consequences of Symptomatic Knee and Hip Osteoarthritis in France

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00481338
Acronym
KHOALA
Enrollment
878
Registered
2007-06-01
Start date
2007-04-30
Completion date
2019-03-31
Last updated
2015-08-03

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

Conditions

Hip Osteoarthritis, Knee Osteoarthritis

Keywords

Cohort, Quality of life, Health resource use, Disability, Prognosis

Brief summary

The aim of the project is to assemble and to follow on a 10-year period a nationwide representative sample of lower limb OA patients. General objectives: To document the natural history and to identify predictive factors of the evolution and consequences of hip and knee OA in terms of pain, functional disability, structural damage, quality of life, autonomy, medical and health care use and cost of disease.

Interventions

PROCEDUREX-rays

X-rays (hip and knee) every 2 years

BIOLOGICALbiological samples

biological sample (blood and urine) every 2 years

OTHERmedical information about osteoarthritis

several questionnaires about pain and function (WOMAC), physical activity (MAQ), quality of life (generic SF-36 and OA specific OAKHQOL/AMIQUAL), comorbidities (FCI), mental status (MMS), heath status (GHQ 28) and health resource consumption

Sponsors

Central Hospital, Nancy, France
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
40 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* male and female aged between 40 and 75 years * symptomatic hip or knee, uni or bilateral OA with clinical diagnosis confirmed by a medical physician and satisfying ACR classification criteria * Representative of prevalent cases in France at the cohort set-up time

Exclusion criteria

* presence of hip or knee joint replacement surgery * comorbidities severe enough to affect quality of life significantly or likely to induce a high health care consumption independently of OA * an history of osteotomy * Patello-femoral osteoarthritis without tibio-femoral osteoarthritis * Other joint diseases of the target joints * adult under legal protection or not able to consent

Design outcomes

Primary

MeasureTime frame
Quality of life, patient reported outcome measuresevery year, up to 10 years

Secondary

MeasureTime frame
health care consumptionevery year, up to 10 years

Countries

France

Outcome results

None listed

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