Evaluation of outcomes from correction of vitamin D levels in residential care facility residents
Phase 3
- Conditions
- Fracturesacute illnesses and exacerbation of chronic conditionsthe need of hospitalisationthe mortality rateVitamin D deficiencyPublic Health - Other public healthMetabolic and Endocrine - Metabolic disordersInjuries and Accidents - Fractures
- Registration Number
- ACTRN12611000950965
- Lead Sponsor
- ACT Government Health Directorate
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 250
Inclusion Criteria
Permenant residents of long-term care facilities in the ACT.
Aged 65 years or more.
Willing to partipate in the study.
Exclusion Criteria
Residents with Aged Care Assesment Team ACFI assessment of 'High' for behaviour (verbal or physical).
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Changes in the frequency of unplanned hospital and GP visits.<br>The research nurse will regularly conduct a data search from participants' medical records at Aged Care Facilities, and ACT Health hospital databases to obtain such information.[14 months following randomisation.];Changes in the frequency of fractures<br>The research nurse will regularly a conduct data search from participants medical records at the Residential Aged Care Facilities, and ACT Health hospital databases to obtain such information.[14 months following randomisation.];Changes in mortality rate.<br>The research nurse will regularly conduct a data search from participants medical records at Residential Aged Care Facilities, and ACT Health hospitals to obtain such information. At the end of the study, formal requests will be made to Australia's National Agency for Health and Welfare Statistics and Information (AIHW) to validate with in-house data collection.[14 months following randomisation.]
- Secondary Outcome Measures
Name Time Method The prevalence of vitamin D deficiency in the studied cohort. At the initial visit, the research nurse will collect baseline blood samples from partcipants to detemine their background vitamin D levels.[14 months following randomisation.]