Respiratory Tract Infection, Vitamin D Deficiency
Conditions
Keywords
Vitamin D, Cholecalciferol, Respiratory tract infection
Brief summary
This is a feasibility double-blind randomised controlled trial in 32 participants. It evaluates the feasibility of a full trial which will examine the efficacy of weekly supplementation of cholecalciferol (vitamin D3) relative to placebo on the subsequent frequency and severity of objectively-verified symptomatic acute respiratory tract infection, overall and as a proportion of detected colonisations of the upper respiratory tract by 9 of the most common aetiologic viral pathogens.
Detailed description
The hypotheses of the full study are: Primary The group treated with vitamin D3 will have a significantly lower frequency of symptomatic respiratory tract infections than controls. Secondary 1. Among persons with detected viral colonisations of the nasopharynx, treated persons will have a lower frequency of symptomatic respiratory tract infection resultant than controls. 2. Treated group will have significantly less severe symptomatic RTIs than controls. 3. Treated group will have significantly shorter symptomatic RTI durations than controls. For the pilot, a cohort of 32 healthy young adults satisfying inclusion criteria will be randomised to cholecalciferol supplement or identical placebo and evaluated daily for the occurrence of RTI symptoms and evaluated weekly for the presence of respiratory colonisation by relevant pathogens using nasopharyngeal swab and polymerase chain reaction using selected pathogen-specific primers. This pilot will demonstrate the logistic feasibility of the proposed study design and provide preliminary data which will inform a larger study to be undertaken next year.
Interventions
DIETARY_SUPPLEMENTCholecalciferol
20,000 IU cholecalciferol capsule, given once weekly for 16 weeks.
DIETARY_SUPPLEMENTPlacebo
Microcellulose capsule identical in appearance to treatment
Sponsors
Royal Hobart Hospital Research Foundation (funding source)
Menzies Institute for Medical Research
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Caregiver, Investigator)
Eligibility
Sex/Gender
ALL
Age
18 Years to 45 Years
Healthy volunteers
Yes
Inclusion criteria
* Students undertaking study at the MS1 building of University of Tasmania Medical Sciences Precinct (17 Liverpool St Hobart TAS) for the full duration between May and September 2012
Exclusion criteria
* Persons who have used tobacco within the 6 months preceding study entry * Persons who have used any vitamin D (cholecalciferol or ergocalciferol) supplements or calcium supplements within the 3 months preceding study entry and/or persons who refuse to not start taking any such supplement during the study * Persons using any immunomodulatory medication, diuretic medication, antiepileptic medication, or barbiturates. * Persons who presently have been diagnosed with any chronic infectious disease (e.g. HIV, tuberculosis), chronic immune deficiency or autoimmune condition, or respiratory condition (e.g. asthma, chronic obstructive pulmonary disease). * Persons who are hypersensitive to vitamin D.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Frequency of validated respiratory tract infections during study period | 17 weeks | Frequency of validated respiratory tract infections during study period. Acute respiratory tract infections defined by respiratory symptoms reported by daily online survey lasting over a day and verified at exam by study nurse. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Proportion of colonisations leading to symptomatic respiratory tract infections | 17 weeks | Proportion of colonisations with respiratory pathogens that go on to symptomatic verified respiratory tract infections. Colonisation detected by nasal swab sampled quantitiative RT-PCR. |
| Severity of respiratory tract infections during study | 17 weeks | Severity (objective and subjective) of respiratory tract infections during the study. Subjective severity of symptoms reported by Likert scale (0-5) for each symptom. Objective severity by number and duration of symptoms. |
| Mean duration of respiratory tract infections during study | 17 weeks | Mean duration of respiratory tract infections during study. Duration defined as number of days from participant-reported symptom onset to sympton resolution, as reported in daily online questionnaire. |
| Frequency of non-respiratory tract infections during study | 17 weeks | Frequency of non-respiratory tract infections during study. Non-respiratory tract infections defined by non-respiratory symptoms reported by daily online survey lasting over a day and verified at exam by study nurse. |
| Concentration of serum 25-hydroxyvitamin D by the end of the study | 17 weeks | Concentration of serum 25-hydroxyvitamin D by the end of the study |
Countries
Australia
Outcome results
None listed