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Evaluation of outcomes from correction of vitamin D levels in residential care facility residents

Phase 3
Conditions
Fractures
acute illnesses and exacerbation of chronic conditions
the need of hospitalisation
the mortality rate
Vitamin D deficiency
Public Health - Other public health
Metabolic and Endocrine - Metabolic disorders
Injuries 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
NameTimeMethod
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
NameTimeMethod
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.]
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