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Vitamin D to Reduce Colds and Asthma Attacks in Young Children

Vitamin D vs. Placebo in the Prevention of Viral-induced Exacerbations in Preschoolers With Asthma: a Pilot RCT

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01999907
Acronym
DIVA-pilot
Enrollment
22
Registered
2013-12-03
Start date
2013-11-30
Completion date
2014-08-31
Last updated
2015-01-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Asthma

Keywords

asthma, virus diseases, pediatric, RCT, steroid

Brief summary

Viral infections are the main cause of asthma attacks in preschoolers, an age group with the highest rate of emergency visits due to asthma. While high doses of inhaled or oral corticosteroids provide benefits, these have been associated with adverse outcomes. Most asthmatic children have lower blood levels of vitamin D compared to non-asthmatic children. Low vitamin D level has been linked to more frequent and more severe asthma attacks as well as with higher dose requirement of inhaled corticosteroid. Recent studies show that vitamin D supplements can reduce the number of asthma attacks triggered by viral infections in children. Unfortunately, most people forget to take vitamin D every day during the fall and winter season as recommended in Canada. A solution is to give a vitamin D bolus by mouth. This has been shown to safely and effectively increase vitamin D levels in children. The investigators hypothesise that a vitamin D bolus given in clinic will sufficiently increase the blood level of vitamin D to prevent the expected winter decline in vitamin D, compared with placebo in preschool-aged children with asthma. This six-month pilot randomized controlled trial aims to: (1) show that a vitamin D bolus is superior to placebo in raising vitamin D levels; (2) record the number of asthma attacks and viral infections in enrolled participants; and (3) identify problems that may call for protocol changes.

Interventions

DIETARY_SUPPLEMENTVitamin D

100,000IU cholecalciferol given in a 2ml dose by mouth at baseline.

DIETARY_SUPPLEMENTdaily vitamin D supplement

Each group receives a daily vitamin D supplement for 6 months, providing 400IU per day.

OTHERPlacebo

placebo given in a 2ml dose by mouth at baseline.

Sponsors

St. Justine's Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
1 Years to 5 Years
Healthy volunteers
No

Inclusion criteria

* children aged 1-5 years * physician-diagnosed asthma as per GINA guidelines * upper respiratory tract infections as the main asthma exacerbation trigger * ≥4 respiratory infections in the past 12 months * ≥1 exacerbation requiring rescue oral steroids in the past 6 months or ≥2 in the previous 12 months.

Exclusion criteria

* extreme prematurity (\<28 weeks gestation) * infants \<12 months of age * breastfed infants with no vitamin D supplementation * recent (\<1 year) immigrants from countries where rickets and malnutrition prevalent * other chronic respiratory disease (broncho-pulmonary dysplasia; cystic fibrosis) * endocrine disorder of calcium/ vitamin D metabolism * disorder/ disease with associated malabsorption (inflammatory bowel disease) * kidney/ liver disease * sickle cell anemia * medications known to interfere with bone metabolism/ vitamin D levels * vitamin D supplementation \>1000 IU/ day in past 3 months * unable to attend medical visit in 3-4 months * plan to leave the province during the next 6 months.

Design outcomes

Primary

MeasureTime frameDescription
serum Vitamin D3 monthsmean change in serum vitamin D from baseline to 3 months

Secondary

MeasureTime frameDescription
adequate serum vitamin D3 monthsdifference in the proportion of children with serum vitamin D ≥75nmol/L at 3 months

Other

MeasureTime frameDescription
Hypercalciuriaany point during the 6 monthsurinary calcium: creatinine ratio \>1.25 (1-2 years) and \>1 (2-5 years) mmol/mmol
Cytokine/ chemokine profile10 dayschange in serum cytokine/ chemokine profile from baseline to 10 days post-bolus dose
duration of viral infectionsin the event of a cold during the 6 monthsnumber of days with respiratory tract symptoms as reported on the parent completed Canadian Acute Respiratory Illness & Flu Scale
exacerbations requiring oral corticosteroids6 monthsnumber of patients with one or more exacerbations requiring oral steroids, as documented by pharmacy dispensation records and medical records
duration of exacerbationsin the event of an exacerbation during the 6 monthsNumber of days with asthma symptoms as reported on the parent-reported 'Asthma Flare-Up Diary for Young Children'
participant retention6 monthspercentage of patients retained until 6 months after randomization
protocol adherence6 months1. participant attendance to all 4 home and clinic visits 2. percentage of patients with all 4 blood and urine tests collected 3. percentage of analyzable viral nasal swabs returned.
severity of exacerbationsin the event of an exacberbation during the 6 months1. area under the curve for β-agonist use as documented by parent of the 'Asthma Flare-Up Diary for Young Children'; 2. need for hospital admission
number of viral infections6 monthsnumber of patients/person-month of observation documented two days 1. parent-reported on the Canadian Acute Respiratory Illness and Flu Scale and 2. Positive viral presence, determined by polymerase chain reaction on nasal sample

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 12, 2026