Osteoporosis With Current Fragility Fracture
Conditions
Keywords
osteoporosis, fragility fracture, secondary prevention
Brief summary
Osteoporosis is a disease characterized by reduced bone mass and increased skeletal fragility, predisposing to an increased fracture risk. The presence of a low trauma fracture is a powerful predictor of future fractures and about 50% of patients with a fragility fracture will suffer a subsequent fracture in the next 10 years (Center Jacqueline R, 2007). Osteoporotic fractures are associated with an increased morbidity and mortality but also high financial costs. However, less than 20% of patients presenting a low trauma fracture receive an appropriate post-fracture osteoporosis management (Little and Eccles, 2010). The hypothesis of a lack of information and an under assessment of consequences by both patients and physicians has been raised to explain this gap between recommended care and usual practices. The aim of the PREVOST program is to assess the efficiency of patient-centered osteoporosis prevention program, after a fragility fracture of the upper limb, to improve post-fracture management of osteoporosis (ie BMD test and / or osteoporosis treatment) in women over 50 years old. This open randomized controlled trial aims to compare the BMD or osteoporosis treatment prescription rate at 6 months after inclusion between two groups: intervention receiving information on fracture and osteoporosis (oral and written), phone call reminders and written information to give to their family physician, and control receiving usual care without information.
Interventions
BEHAVIORALOsteoporosis prevention program
Women will receive an oral information and advices on osteoporosis, a written leaflet on osteoporosis (risk factors, diagnosis, prevention and treatments), a letter and a leaflet on osteoporosis management to give to their family physician and phone call reminders (D15, D30, D45) to advise them to consult their family physician and, if they have a BMD prescription, to perform their BMD
Sponsors
Hospices Civils de Lyon
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE
Eligibility
Sex/Gender
FEMALE
Age
50 Years to 85 Years
Healthy volunteers
No
Inclusion criteria
* Women aged over 50 years * with a fragility fracture of wrist or humerus that occurred in the past 6 months * treated in an emergency department or orthopedic department * who signed the consent form
Exclusion criteria
* no signed consent * previous history of femoral neck fracture * poly-trauma or accident * patients under osteoporosis treatment * patients who performed a BMD test in the past 6 months * patients with severe renal impairment, hyperthyroidism, bone primary or secondary malignancy. * legal disability * difficulty in understanding French * psychiatric disorder
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Proportion of women in the 2 groups who initiated a management of osteoporosis at 6 months (BMD or osteoporosis treatment prescription). | 6 months after inclusion | At 6 months, women will be asked whether or not they received a BMD test prescription and/or an osteoporosis treatment prescription by their physician. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Proportion of women in the two groups who performed BMD at 6 months | 6 months after inclusion | At 6 months, women who received a BMD prescription will be asked whether or not they performed a BMD test; if they realized a BMD test, their result will be asked. |
| Proportion of women in the two groups with an increased perception of fracture risk. | 6 months after inclusion | Women will answer the same questionnaire at inclusion and at 6 months to assess their fracture risk perception. |
| Proportion of women in the two groups who changed their behaviour in order to prevent future fractures: regular practice of physical activity, dairy products consumption and calcium and vitamin D supplementation. | 6 months after inclusion. | Women will answer the same questionnaire at inclusion and at 6 months to assess their behaviour towards fracture risk or prevention of osteoporosis: physical activity, dairy products consumption and calcium and vitamin D supplementation |
| Proportion of women who improved their knowledge about osteoporosis | 6 months after inclusion | Women will answer the same questionnaire at inclusion and at 6 months to assess their osteoporosis perception and knowledge (risk factors, severity,consequences, treatments) |
Countries
France
Outcome results
None listed