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Secondary Prevention of Osteoporosis
This study has been completed.
Study NCT00421343   Information provided by National Institute on Aging (NIA)
First Received: January 10, 2007   Last Updated: August 28, 2008   History of Changes

January 10, 2007
August 28, 2008
February 2007
June 2008   (final data collection date for primary outcome measure)
Changes in functional status and muscle strength [ Time Frame: 6-months post fracture ] [ Designated as safety issue: No ]
Changes in functional status and muscle strength 6-months post fracture
Complete list of historical versions of study NCT00421343 on ClinicalTrials.gov Archive Site
  • Changes in vitamin D levels [ Time Frame: 6 months ] [ Designated as safety issue: No ]
  • satisfaction with the intervention [ Time Frame: 6 months ] [ Designated as safety issue: No ]
  • reasons for adherence/non-adherence with the intervention [ Time Frame: 6 months ] [ Designated as safety issue: No ]
  • Changes in vitamin D levels
  • satisfaction with the intervention
  • reasons for adherence/non-adherence with the intervention
 
Secondary Prevention of Osteoporosis
Secondary Prevention of Osteoporosis: A Window of Opportunity in the Acute Rehabilitation Setting

The purpose of this study is to develop and implement an evidence based protocol for the secondary prevention of osteoporotic fractures and falls, and to determine how compliance with this intervention improves muscle strength and functional status following a fracture.

Following a fracture, few persons are screened or treated for osteoporosis (Feldstein et al). It is not surprising, then, that the risk of future osteoporotic fractures remains high. Although little data exists on the secondary prevention of osteoporosis, calcium, vitamin D, and bisphosphonates have all been shown to be effective in the primary prevention of osteoporotic fractures, and they are likely beneficial in reducing secondary fractures as well. Targeting falls prevention is another approach that is likely effective in reducing the risk of fracture.

In the U.S., acute rehabilitation (rehab) settings offer a unique environment to initiate osteoporotic therapy. Therefore, this study will develop and implement evidence based interventions for the secondary prevention of osteoporotic fractures in the acute rehab setting with the following objectives:

Specific Aim I: Assess overall compliance with pharmacological and non-pharmacological interventions initiated in an acute rehab setting following a fragility fracture. Hypothesis: Non-compliant participants are less likely to show improvement in functional status, muscle strength, or vitamin D levels following the intervention.

Specific Aim II: Describe the incidence of fragility fractures and falls in participants at 6-months and one-year following the osteoporotic intervention introduced during acute rehab. Hypothesis: Similar to community based studies, a number of participants will go on to experience repeat falls and resulting fractures within one-year of follow-up. Compliant participants are less likely to experience falls and fractures.

Specific Aim III: Confirm the high prevalence of vitamin D deficiency in a rehab setting. Describe the relationship between changes in vitamin D levels in participants between baseline and 6-month follow-up and changes in functional outcomes. Hypothesis: There will be a direct association between a change in vitamin D levels and a change in functional status.

Consecutive individuals admitted with the primary or secondary diagnosis of fracture in the rehabilitation unit of Hebrew Rehabilitation Center will be offered enrollment. All participants enrolled will receive the same intervention: calcium, vitamin D, a weekly oral bisphosphonate, and falls prevention interventions. Specific interventions for preventing falls include optimization of visual acuity, a review of medications associated with falls, personalized exercises to improve strength and balance, and a home hazards safety evaluation when indicated.

All participants will have their functional status, muscle strength, and vitamin D level measured at baseline during their rehab stay. At the six-month follow-up, a home visit will be performed for all participants to again assess functional status, muscle strength, vitamin D level, satisfaction with the intervention, and reasons for non-compliance. A history of interim falls and fractures will be collected by telephone interviews, during home nursing visits, and during the exit 6-month visit.

Phase III
Interventional
Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Efficacy Study
Osteoporosis
  • Drug: alendronate with cholecalciferol
  • Drug: calcium carbonate with cholecalciferol
  • Behavioral: Falls prevention measures
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Completed
27
June 2008
June 2008   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Admitted to rehab unit with the primary or secondary diagnosis of fracture
  • English speaking
  • Cognitively able to provide consent or health care proxy available and willing to provide consent
  • Willing to cooperate

Exclusion Criteria:

  • Pathologic or periprosthetic fractures
  • Creatinine clearance less than 15ml/minute
  • Severe hypocalcemia
  • Esophageal stricture or achalasia
  • Taking other treatment for osteoporosis besides calcium or vitamin D in the past 6-months
  • History of kidney stones in the past 6-months
Both
65 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00421343
Sarah D. Berry, MD, MPH, Harvard University, Hebrew Rehabilitation Center
AG0074, 5 T32 AG023480-03
National Institute on Aging (NIA)
  • Merck
  • GlaxoSmithKline
Principal Investigator: Sarah D Berry, MD, MPH Harvard University, Hebrew Rehabilitation Center
National Institute on Aging (NIA)
August 2008

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP