- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT03310242
Comparison of Sunlight Exposure and Vitamin D Supplementation on Serum 25-hydroxyvitamin D Levels
Comparison of Sunlight Exposure and Oral Vitamin D Supplementation on Serum 25-hydroxyvitamin D Concentration and Metabolic Markers in Korean Young Adults: a Randomized Clinical Trial
Studieoversigt
Status
Betingelser
Intervention / Behandling
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Ikke anvendelig
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- Serum 25(OH)vitamin D < 12ng/mL
- age between 18 and 39 years
- Korean men and women
Exclusion Criteria:
- Vitamin D supplementation within 2 months
- Photosensitivity or UV allergy
- History of hyperparathyroidism/hypercalciuria/kidney stone/skin cancer and other cancer
- Under medication for hypertension, dyslipidemia, and diabetes
- Intake of photosensitive medicine during study period
- Exposure of strong UV (e.g., beach, sun tanning) during study period
- Pregnant/breast-feeding women
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Firedobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Sunlight Exposure
Everyday sunlight exposure around noon for 20-30 minutes for 8 weeks
|
|
|
Eksperimentel: Vitamin D Supplementation
Supplementation of vitamin D3 500 IU/day for 8 weeks
|
- Supplementation of vitamin D3 500 IU/day for 8 weeks
|
|
Placebo komparator: Placebo
Intake of placebo for 8 weeks
|
- Intake of placebo for 8 weeks
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Serum 25(OH)D
Tidsramme: Baseline, 4 week, and 8 week
|
Changes in serum 25(OH)D levels in ng/mL
|
Baseline, 4 week, and 8 week
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
BMI
Tidsramme: Baseline, 4 week, and 8 week
|
Weight and height will be combined to report BMI in kg/m^2
|
Baseline, 4 week, and 8 week
|
|
Systolic blood pressure
Tidsramme: Baseline, 4 week, and 8 week
|
Systolic blood pressure changes in mmHg
|
Baseline, 4 week, and 8 week
|
|
Diastolic blood pressure
Tidsramme: Baseline, 4 week, and 8 week
|
Diastolic blood pressure changes in mmHg
|
Baseline, 4 week, and 8 week
|
|
Lipid panel
Tidsramme: Baseline and 8 week
|
Serum total cholesterol, triglycerides, HDL cholesterol, and LDL cholesterol in mg/dL
|
Baseline and 8 week
|
|
Fasting glucose
Tidsramme: Baseline and 8 week
|
Serum fasting glucose in mg/dL
|
Baseline and 8 week
|
|
AST
Tidsramme: Baseline and 8 week
|
Serum AST levels in mg/dL
|
Baseline and 8 week
|
|
ALT
Tidsramme: Baseline and 8 week
|
Serum ALT levels in mg/dL
|
Baseline and 8 week
|
|
GGT
Tidsramme: Baseline and 8 week
|
Serum AST, ALT, and GGT levels in mg/dL
|
Baseline and 8 week
|
|
Intact PTH
Tidsramme: Baseline and 8 week
|
Serum intact PTH levels in mg/dL
|
Baseline and 8 week
|
|
Whole body BMD and BMC
Tidsramme: Baseline and 8 week
|
Whole body BMD (g/cm^2) and BMC (kg) measured by DEXA
|
Baseline and 8 week
|
|
Lean body mass, fat mass, and percent fat
Tidsramme: Baseline and 8 week
|
Lean body mass (kg), fat mass (kg), and percent fat (%) measured by DEXA
|
Baseline and 8 week
|
|
Lean body mass, muscle mass, skeletal muscle mass, fat mass, and percent fat
Tidsramme: Baseline, 4 week, and 8 week
|
Lean body mass (kg), muscle mass (kg), skeletal muscle mass (kg), fat mass (kg), and percent fat (%) measured by body impedance analysis
|
Baseline, 4 week, and 8 week
|
|
EQ-5D-5L
Tidsramme: Baseline, 4 week, and 8 week
|
Quality of life measured using EQ-5D-5L scale. The EQ-5D is a standardised measure of health status developed by the EuroQol Group in order to provide a simple, generic measure of health status. In description part, health status is measured in terms of five dimensions (5D); mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. The respondents self-rate their level of severity for each dimension using three-level (EQ-5D-3L) or five-level (EQ-5D-5L) scale. The 5-level version of EQ-5D (EQ-5D-5L) was developed to improve such constraints of the three-level scale. EQ-5D-5L scale can define 3,125 (=5^5) different health states, and the 5-digit number can be converted into a preference weight which is also referred to as a single weighted index score. The index score of a value set derived from the general population sample can be regarded as a "societal valuation of the respondent's health state" in that country. |
Baseline, 4 week, and 8 week
|
Samarbejdspartnere og efterforskere
Efterforskere
- Ledende efterforsker: Hee-Kyung Joh, PhD, Seoul National University College of Medicine/Seoul National University Hospital
Publikationer og nyttige links
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- H-1504-112-668
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
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