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Vitamin D Supplementation and Muscle Characteristics in Trained Subjects

7. september 2017 opdateret af: Inland Norway University of Applied Sciences

Effects of 12 Weeks of Vitamin D Supplementation on Muscle Characteristics in Trained Subjects

This study evaluates the effect of vitamin D supplementation on outcomes muscle performance and characteristics in 70 trained healthy individuals (18-40 years of age). Subjects will be allocated to ingest either vitamin D (35) or placebo (35) in a double-blinded fashion

Studieoversigt

Status

Afsluttet

Detaljeret beskrivelse

Vitamin D insufficiency compromises muscle functionality, leading to changes in muscle mass and strength, manifested at the cellular level. While this is increasingly recognized as a problem for individuals with vitamin D deficiency (typically 25(OH)D < 25 nmol/l), there is no general consensus for the remainder of the vitamin D-spectra. This lack of knowledge is probably linked to the variation in protocols of studies that have investigated the physiological role of vitamin D. These variations vary from aspects such as interventional vs observational studies to aspects related to subject characteristics such as age, health and training status. In this project, we will evaluate the effects of 12 weeks of vitamin D supplementation (2000 IU/day) on muscle performance and characteristics in 70 trained healthy individuals (18-40 years of age). Subjects will be allocated to either a vitamin D (35) or a placebo group (35) in a double-blinded manner. They will be instructed to continue their ordinary modes and frequency of training.

We anticipate baseline vitamin D levels in blood (and hence changes in vitamin D obtained through supplementation), measured as 25(OH)D, to be a major determinant of the efficacy of the intervention. This means that we expect individuals with low baseline levels of 25(OH)D to display more pronounced changes in functional and biological outcome measures than those with high baseline values. Such a scenario could be related to an inability of our protocol to increase blood levels of 25(OH)D in individuals with higher physiological levels of vitamin D (which essentially means that ingestion of vitamin D3 is leveled out or exceeded by elimination of vitamin D derivatives). Alternatively, it may be related to inabilities of tissues to respond to the resulting elevation in vitamin D levels. To study the individual variation in vitamin D responses, data on both functional and biological variables will be divided into quartiles based on baseline 25(OH)D-levels, whereupon comparisons will be made between the low-end and high-end quartile. Individual variation will also be assessed using a mixed model approach.

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

71

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

      • Lillehammer, Norge
        • Lillehammer University College

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år til 40 år (Voksen)

Tager imod sunde frivillige

Ja

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

- Individuals that have performed strength and / or endurance exercise training at least 3 X week for at least 6 months prior to the study

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Tredobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Vitamin D3
Vitamin D3 capsules for 12 weeks (2000 IU daily, equivalent to 50 ug)
Vitamin D3 opløst i olivenolie, indkapslet
Andre navne:
  • cholecalciferol
Placebo komparator: Placebo
Placebo capsules for 12 weeks (the number of daily capsules will match that of the vitamin D-group)
Olivenolie, indkapslet

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Lower body maximal dynamic strength
Tidsramme: wk 0, wk12
Changes in the ability of lower body muscles to exert maximal force during a dynamic movement
wk 0, wk12
Muscle fiber composition
Tidsramme: wk0, wk12
Changes of the muscle fiber composition of musculus vastus lateralis in a 2X to 2A direction, measured using mRNA profiling
wk0, wk12

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Gene expression in muscle
Tidsramme: wk0, wk12
Changes in RNA abundances in musculus vastus lateralis, measured at the level of single genes
wk0, wk12
Vitamin D in blood
Tidsramme: wk0, wk12
Changes in levels of 25(OH)D in blood
wk0, wk12
Steroid hormones in blood
Tidsramme: wk0, wk12
Changes in levels of steroid hormones in blood
wk0, wk12
Muscular endurance
Tidsramme: wk0, wk12
Changes in the ability of muscles to perform repeated dynamic contractions at submaximal loads (50% of 1 repetition maximum)
wk0, wk12
Upper body maximal dynamic strength
Tidsramme: wk0, wk12
Changes in the ability of upper body muscles to exert maximal force during dynamic movements
wk0, wk12

Andre resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Training diary
Tidsramme: From 1 month prior to study to post test (w12)
Diary that includes information on type of training, duration and intensity performed
From 1 month prior to study to post test (w12)
Vitamin D-intake diary
Tidsramme: From 1 month prior to study to post test (w12)
Diary withthat includes information on approximate intake of vitamin D from sources other than the study-specific supplement, including ingestion of fish, seafood and vitamin D-supplement
From 1 month prior to study to post test (w12)
Sun exposure diary
Tidsramme: From 1 month prior to study to post test (w12)
Diary that includes information on exposure to solarium or sun in countries south of Norway
From 1 month prior to study to post test (w12)

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Samarbejdspartnere

Efterforskere

  • Ledende efterforsker: Håvard Nygaard, MSc, Inland Norway University of Applied Sciences

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart

1. november 2015

Primær færdiggørelse (Faktiske)

28. februar 2017

Studieafslutning (Faktiske)

28. februar 2017

Datoer for studieregistrering

Først indsendt

5. november 2015

Først indsendt, der opfyldte QC-kriterier

5. november 2015

Først opslået (Skøn)

6. november 2015

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

8. september 2017

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

7. september 2017

Sidst verificeret

1. marts 2017

Mere information

Begreber relateret til denne undersøgelse

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

Kliniske forsøg med Vitamin D3

Abonner