Sunlight Exposure and Vitamin D in Children

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Lesley Rhodes, University of Manchester
ClinicalTrials.gov Identifier:
NCT01477827
First received: November 18, 2011
Last updated: January 14, 2013
Last verified: January 2013
  Purpose

The purpose of this study is to examine the amount of sunlight exposure and vitamin D status of adolescent schoolchildren in each season throughout the year.


Condition Intervention
Healthy Schoolchildren
Other: None - observational study

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Sunlight Exposure and Vitamin D Status of Children in the UK

Resource links provided by NLM:


Further study details as provided by University of Manchester:

Primary Outcome Measures:
  • Serum concentration of 25-hydroxyvitamin D [ Time Frame: Approximately every 3 months ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Amount of sunlight exposure received [ Time Frame: Approx every 3 months ] [ Designated as safety issue: No ]
    Exposure to sunlight over 7 consecutive days is measured using polysulphone badges with one badge for weekdays and a second badge for the weekend.

  • Dietary intake of vitamin D [ Time Frame: Approximately every 3 months ] [ Designated as safety issue: No ]
    Intake of foods containing vitamin D is recorded for a one week period and the average daily intake determined.


Enrollment: 125
Study Start Date: June 2010
Study Completion Date: July 2012
Primary Completion Date: July 2012 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
Healthy volunteers
Healthy adolescents aged 12-15 years
Other: None - observational study
N/A

  Eligibility

Ages Eligible for Study:   12 Years to 15 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population

Schoolchildren in Greater Manchester

Criteria

Inclusion Criteria:

  • Healthy school children aged 12-15 years
  • White Caucasian
  • Male or female

Exclusion Criteria:

  • History of photosensitivity disorder
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01477827

Locations
United Kingdom
Salford Royal NHS Foundation Trust
Manchester, United Kingdom, M6 8HD
Sponsors and Collaborators
University of Manchester
Investigators
Principal Investigator: Lesley Rhodes, MBBS MD FRCP University of Manchester
  More Information

No publications provided

Responsible Party: Lesley Rhodes, Professor of Experimental Dermatology, University of Manchester
ClinicalTrials.gov Identifier: NCT01477827     History of Changes
Other Study ID Numbers: Bupa Protocol 1
Study First Received: November 18, 2011
Last Updated: January 14, 2013
Health Authority: United Kingdom: Research Ethics Committee

Additional relevant MeSH terms:
Vitamin D
Vitamins
Bone Density Conservation Agents
Physiological Effects of Drugs
Pharmacologic Actions
Micronutrients
Growth Substances

ClinicalTrials.gov processed this record on April 16, 2014