Skip to content

Effects of vitamin D supplementation in physically active adults

Effect of vitamin D supplementation on resting metabolic rate, body composition and strength in physically active adults

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12620000896976
Enrollment
31
Registered
2020-09-11
Start date
2019-03-23
Completion date
2019-05-27
Last updated
2020-09-21

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

Conditions

None listed

Brief summary

Most of our vitamin D comes from spending time in the sun, but also a little comes from our diet. Importantly, research suggests that the amount of vitamin D that you have may affect the health of your muscles and therefore your strength, body composition and the amount of energy that your body uses at rest. However, we don’t know lots of things about this relationship and therefore we need to investigate it further. This is important because vitamin D may assist people to achieve a healthier body composition and perhaps help with the progression of exercise training (e.g., increasing muscle strength). The results of this study will help health professionals to clarify if higher levels of vitamin D are beneficial for achieving optimal muscle function and body composition.

Interventions

Participants completed two testing sessions (one pre-supplementation and another post-supplementation) over approximately 13 weeks. First, participants completed initial assessments, including an assessment of RMR, body composition, muscular strength and power, and hematological markers [total and free plasma 25(OH)VitD, Ca2+ and parathyroid hormone] between week 0 and 1. Data collection started after the summer season (March/April/May, Western Australia) to increase the chance of individuals be

Participants completed two testing sessions (one pre-supplementation and another post-supplementation) over approximately 13 weeks. First, participants completed initial assessments, including an assessment of RMR, body composition, muscular strength and power, and hematological markers [total and free plasma 25(OH)VitD, Ca2+ and parathyroid hormone] between week 0 and 1. Data collection started after the summer season (March/April/May, Western Australia) to increase the chance of individuals being VitD sufficient at the baseline and to optimize the chance of participants reaching higher serum total concentration (= 120 nmol·L-1) at the end of the supplementation period. Following pre-testing, participants were matched for sunlight exposure and randomly allocated in a double-blind and counterbalanced manner to the VitD3 group (total n = 17, female n = 11; 50 IU·kg-1 body-mass [BM]·day-1 Elite Vitamin D3, Healthspan Ltd®, United Kingdom [UK], batch tested by Informed-Sport, LGC Limited, UK) or placebo (total n = 14, female n = 8; dextrose, Glucodin, iNova Pharmaceuticals, Australia) supplement group for 12 weeks. All doses were concealed in opaque gelatin capsules (oral supplementation) and organized in sequentially numbered envelopes to ensure that participants and the testing researcher were blinded to group allocations. This dosing strategy was selected because it has been associated with a positive effect on strength performance in previous research. In the middle of the study (week 7) hematological markers were again assessed to measure VitD concentration and check for any possible adverse effects of supplementation. The frequency of the intervention administration was once a day for 12 weeks. Then, following 12 weeks of supplementation, participants repeated the pre-supplementation testing at the same time of day and referring back to their three-day food diary to ensure that they were similarly prepared to perform. Adequate and optimal VitD status were defined as 25(OH)D between 50-100nmol·L-1 and > 100 nmol·L-1, respectively, based on previous research that suggests that these concentrations may be related to optimal skeletal muscle outcomes. Participants were in contact with the main researcher weekly by personal text messages and email, to ensure training and supplementation adherence and report any perceived side-effects from the supplementation (self-report). Vitamin D3 supplementation was distributed to participants fortnightly and the capsules left were counted to determine compliance. A three-day food diary will be kept to measure dietary intake through the whole study (pre, middle and post supplementation period). First, participants recorded the amount of food, fluid and supplements consumed during 3 consecutive days (2 weekdays and 1 day of the weekend), after having received detailed instructions about how to complete their dietary intake. This diet monitoring period is considered adequate for the estimation of habitual energy and macronutrient consumption. Then each food record was briefly reviewed by a nutritionist together with each participant to ensure that sufficient detail is captured. Food records were analysed using Foodworks® (V9, Xyris Australia). Each individual will be encouraged to follow similar eating patterns throughout the study to minimise deviations in macronutrients, and vitamin and mineral intake.

Sponsors

Curtin University
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Prevention
Masking
Blinded (masking used) (Subject, Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

- adults, 18-35 years old -exercising at least three times per week with at least two of those sessions involving resistance training; - no history of VitD3 supplementation in the last month; - no current injuries that would prevent them from completing strength testing; - no current use of multivitamins, medication, or other supplements that are related with VitD metabolism and body composition [including calcium, thyroxine, creatine and thermogenic supplements]). - available to complete the tests at Curtin University and PathWest lab

Exclusion criteria

none

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026