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The Effects of Vitamin D Supplementation on Aerobic Fitness in Athletes (VDAF)

U

Ulster University

Status and phase

Completed
Phase 4

Conditions

Aerobic Fitness (VO2max)

Treatments

Dietary Supplement: Placebo
Dietary Supplement: Vitamin D

Study type

Interventional

Funder types

Other

Identifiers

NCT02278172
REC14.0087

Details and patient eligibility

About

The primary aim of the study is to identify if vitamin D3 supplementation influences VO2max in athletes.

Secondary aims are to determine if vitamin D3 supplementation impacts on measures of muscle function, lung function, body composition, immune function and the self-reported incidence of upper respiratory tract infection.

This double-blind, randomised, placebo-controlled trial is of parallel design and will aim to recruit a total of 50 athletes randomised into either a placebo or treatment group for a 12-week intervention.

Enrollment

44 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Athletes whose sport does not primarily consist of an anaerobic component
  • Apparently healthy
  • Over the age of 18

Exclusion criteria

  • Resting arterial hypertension
  • Individuals who are not an athlete at a University/local sports team
  • Athletes who predominantly utilise anaerobic energy systems
  • Athletes under the age of 18
  • Those that have consumed a supplement containing vitamin D (greater than 400IU/day) or iron supplements for up to 30 days prior to starting the study
  • Those with health conditions identified by the screening questionnaire
  • Individuals that are on prescribed medication that is known to affect vitamin D metabolism
  • Those following a vegan diet
  • Those with a physical disability that would prevent successful completion of the exercise test
  • Those who have either had a sun holiday in the 4 weeks prior to starting the study
  • Those planning a sun holiday during the intervention period

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

44 participants in 2 patient groups, including a placebo group

Vitamin D3 3000IU (75μg)
Active Comparator group
Description:
Treatment solution delivered via oral spray once daily for 12-weeks
Treatment:
Dietary Supplement: Vitamin D
Placebo
Placebo Comparator group
Description:
Placebo solution delivered via oral spray once daily for 12-weeks
Treatment:
Dietary Supplement: Placebo

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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