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Vitamin D DeficiencyNCT01385085

Impact of Work Environment Absent of Natural Light on Vitamin D Levels

An observational study of Vitamin D Deficiency, run by Medical Corps, Israel Defense Force.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Three types of workers exposed to different levels of natural sunlight will be tested for Vitamin D blood level, PTH, Ca, P, albumin and alkaline phosphatase. In addition, each tested worker will be asked to fill a questionnaire for demographic, medical and personal habit information. Read more about this study

Who is it for?
Ages 18 to 45 yearsHealthy volunteers can take part
Conditions the study is for
Vitamin D Deficiency
How many people
300 participants
Where
No sites listed yet
Study dates
Nov 2011to not given
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 45 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Study population: People employed in three types of natural sunlight exposure.

Who may be able to join

  • people employed in their current work place at least 6 months,

Who cannot join

  • people who consume food additives containing Vitamin D.
  • people who have a chronic illness which harms the Vitamin D absorption, such as Celiac, chronic Pancreatitis, Cystic Fibrosis and IBS.
  • people who have a chronic illness which harms Vitamin D metabolism, such as chronic hepatitis, kidney insufficiency and Nephrotic Syndrome.
  • pregnant women.
  • people who require prescribed medicine like steroids, anti-convulsion, and HIV treatments.

About this study

Three types of workers exposed to different levels of natural sunlight will be tested for Vitamin D blood level, PTH, Ca, P, albumin and alkaline phosphatase.

In addition, each tested worker will be asked to fill a questionnaire for demographic, medical and personal habit information.

Keywords
Vitamin D, Sunlight, Deficiency
Medical subject headings
Vitamin D Deficiency

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT01385085
Study groupRoleWhat they receive
No natural sunlightone group works in a basement with no natural sunlight
Low level of Natural Sunlightthe second group work in offices with unopenable windows.
High level of Natural SunlightThe third group works outdoors.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted29 Jun 2011 (estimated)
  2. Study startNov 2011

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case crossover
Time perspective
Cross-sectional
Enrolment
300 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01385085
Sponsor's protocol ID
922-2010-IDF-CTIL
Status last verified
Jun 2011
First submitted
28 Jun 2011
Last updated
29 Jun 2011
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

An observational study of Vitamin D Deficiency, run by Medical Corps, Israel Defense Force.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 29 Jun 2011. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 Jun 2011.

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