Cholecalciferol and Flu Vaccine in Treating Healthy Participants

N/ATerminatedNCT01561989

Roswell Park Cancer Institute11 enrolled

Overview

This randomized clinical trial studies cholecalciferol and flu vaccine in treating healthy participants. Cholecalciferol may increase the immunologic response of flu vaccine in healthy participants. Flu vaccine may help the body build an immune response and help prevent flu

PRIMARY OBJECTIVES: I. To examine the effect of 25-hydroxy vitamin D3 levels on the immunologic response (antibody responses week 4 \[4 weeks (+/- 7 days)\] post-vaccination) to the injectable seasonal (2011-2012) trivalent influenza vaccine among Roswell Park Cancer Institute (RPCI) employees. (Observational component) II. To examine the effect of vitamin D3 (cholecalciferol) supplementation on the immunologic response (antibody response Week 16 \[4 weeks (+/- 7 days)\] post-vaccination) to the injectable seasonal (2012-2013) trivalent influenza vaccine among RPCI employees. (Intervention component) SECONDARY OBJECTIVES: I. To track occurrences of flu-like illness in the study population from November 1, 2011 through April 1, 2012, using a standardized epidemiologic questionnaire. (Observational component) II. To determine the relationship between 25-hydroxy vitamin D3 levels at time of vaccination and its immunologic responses Week 20 (8 weeks \[+/- 7 days\]) and Week 24 (12 weeks \[+/- 7 days\]) following administration of the injected seasonal (2012-2013) trivalent influenza vaccine. (Intervention component) III. To track occurrences of flu-like illnesses in the study population from November 2012 through April 2013, using a standardized epidemiologic questionnaire. (Intervention component) IV. To evaluate the association between single-nucleotide polymorphisms (SNPs) and polymorphisms in the deoxyribonucleic acid (DNA) sequence of vitamin-D3 metabolizing enzymes, measures of vitamin-D3 metabolism (24,25 hydroxy \[OH\] vitamin D3) and response to seasonal (2012-201) trivalent influenza vaccine. (Intervention component) OUTLINE: Patients are randomized to 1 of 2 treatment arms. ARM I: Patients receive low-dose cholecalciferol orally (PO) once daily (QD) for 12 weeks, followed by the seasonal (2012-2013) trivalent influenza vaccine intramuscularly (IM). ARM II: Patients receive high-dose cholecalciferol PO QD for 12 weeks, followed by the seasonal (2012-2013) trivalent influenza vaccine IM. After completion of study treatment, patients are followed up periodically.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

DOUBLE

Enrollment

Conditions

Healthy, no Evidence of Disease

Interventions

cholecalciferolDIETARY_SUPPLEMENT

Given PO

questionnaire administrationOTHER

Ancillary studies

trivalent influenza vaccineBIOLOGICAL

Given IM

Eligibility

Sex: ALLMin age: 18 YearsMax age: 64 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Healthy individuals seen at the Employee Health Clinic who will be eligible to receive influenza vaccine * Willingness to comply with study expectations * subject or legal representative must understand the investigational nature of this study and sign an Independent Ethics Committee/Institutional Review Board approved written informed consent form prior to receiving any study related procedure * INTERVENTION COMPONENT ONLY: * Willing to suspend use of any other vitamin D supplementation during the 3 month treatment interval; if currently using \> 2,000 IU/day of vitamin D supplementation, must suspend use 30 days prior to enrollment Exclusion criteria: -not RPCI employee

Locations (1)

Roswell Park Cancer Institute

Buffalo, New York, United States

Outcomes

Primary Outcomes

Effect of 25-hydroxy Vitamin D3 Levels on Immunologic Response (Antibody Responses) to Injectable Seasonal (2011-2012) Trivalent Influenza Vaccine (Observational Component)

Descriptive statistics and chi-square tests will be used to assess for differences in the occurrence of self-reported flu-like illnesses in the study population.

Time frame: At 4 weeks post-vaccination

Effect of Cholecalciferol Supplementation on Immunologic Response (Antibody Response) to Injectable Seasonal (2012-2013) Trivalent Influenza Vaccine (Intervention Component)

Descriptive statistics will be used to assess for differences in the occurrence of self-reported flu-like illnesses in the study population. Will be estimated with confidence intervals at each time point. Tested by Wald Chi-square test, and the odds ratio (with confidence intervals) will be reported.

Time frame: Up to 24 weeks post-vaccination

Secondary Outcomes

Occurrences of Flu-like Illness (Observational Component)

occurrences of flu-like illness

Time frame: Up to April 1, 2012

Relationship Between 25-hydroxy Vitamin D3 Levels at Time of Vaccination and Immunologic Responses Following Administration of the Injected Seasonal (2012-2013) Trivalent Influenza Vaccine (Intervention Component)

Relationship between 25-hydroxy vitamin D3 levels at time of vaccination and immunologic responses following administration of the injected seasonal (2012-2013) trivalent influenza vaccine (Intervention component)

Time frame: Up to week 24

Occurrences of Flu-like Illnesses (Intervention Component)

occurrences of flu like illness (intervention arm)

Time frame: From initial treatment until the end of study (April 1, 2012); up to 24-weeks.

Data from ClinicalTrials.gov

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