Trial Review

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Trial registered on ANZCTR


Registration number
ACTRN12612000031864
Ethics application status
Not yet submitted
Date submitted
4/01/2012
Date registered
9/01/2012
Date last updated
9/01/2012
Type of registration
Prospectively registered

Titles & IDs
Public title
Vitamin D and muscle strength in female dancers and gymnasts
Scientific title
The effect of 12 months of cholecalciferol supplementation on muscle strength, bone mineral density and respiratory infections in female adolescent gymnasts and dancers
Secondary ID [1] 279679 0
Nil Known
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Nutritional status of adolescent female gymnasts and dancers 285478 0
Muscle strength in female dancers and gymnasts 285479 0
Bone mineral density in female dancers and gymnasts 285501 0
Respiratory infections in female dancers and gymnasts 285502 0
Nutritional status of female dancers and gymnasts 285503 0
Condition category
Condition code
Diet and Nutrition 285658 285658 0 0
Other diet and nutrition disorders
Musculoskeletal 285695 285695 0 0
Normal musculoskeletal and cartilage development and function

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
12 month supplementation trial with vitamin D3 (cholecalciferol) 1.25mg (50,000 IU) oral tablet, once per month
Intervention code [1] 283947 0
Other interventions
Comparator / control treatment
placebo in the form of oral tablet identical in appearance to the intervention tablet but with no active ingredients, taken once per month
Control group
Placebo

Outcomes
Primary outcome [1] 286208 0
muscle strength: dominant and non-dominant hand-grip measured using grip-strength dynamometer, quadriceps, hamstrings, knee extensors and flexors using an isokinetic dynamometer (Biodex 4), and jump height using a flight-time calculating jump mat.
Timepoint [1] 286208 0
6 and 12 months
Primary outcome [2] 286209 0
bone mineral density assessed at lumbar spine and proximal femure using dual energy x-ray absorptiometry (DXA) scan (Hologic Discovery A).
Timepoint [2] 286209 0
12 months
Primary outcome [3] 286225 0
Respiratory infections recorded using the Wisconsin Upper Respiratory Symptom survey
Timepoint [3] 286225 0
6 and 12 months
Secondary outcome [1] 295393 0
Iron status - full iron studies from venous blood sample including haemoglobin, serum ferritin, and soluble transferrin receptor
Timepoint [1] 295393 0
baseline
Secondary outcome [2] 295411 0
dietary intake from 4-day food diary (analysed using Foodworks software) and validated food frequency questionnaire to assess consumption of iron containing foods.
Timepoint [2] 295411 0
Baseline
Secondary outcome [3] 295412 0
body composition using dual x-ray absorptiometry, full body scan (Hologic Discovery A)
Timepoint [3] 295412 0
Baseline

Eligibility
Key inclusion criteria
Participating in gymnastics or dance at least 5 hours per week
Minimum age
13 Years
Maximum age
18 Years
Sex
Females
Can healthy volunteers participate?
Yes
Key exclusion criteria
Recent (within 2 months) or current use of vitamin D supplements including cod liver oil, smoker

Study design
Purpose of the study
Prevention
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Participants will be recruited by advertisements in various media. Once enrolled, they will be matched in pairs by (a) type of activity, and (b) age. Participants will receive either a vitamin D supplement or identical (in appearance) placebo pill once per month.Randomisation will be conducted by a 3rd party not associated with the study.
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Participants will be randomised using simple randomisation using a computer generated randomisation table (www.randomization.com)
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?



Intervention assignment
Parallel
Other design features
Phase
Phase 4
Type of endpoint/s
Efficacy
Statistical methods / analysis

Recruitment
Recruitment status
Not yet recruiting
Date of first participant enrolment
Anticipated
5/04/2012
Actual
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
Sample size
Target
100
Accrual to date
Final
Recruitment outside Australia
Country [1] 4038 0
New Zealand
State/province [1] 4038 0
Auckland

Funding & Sponsors
Funding source category [1] 284445 0
University
Name [1] 284445 0
Massey University Research Fund
Country [1] 284445 0
New Zealand
Primary sponsor type
University
Name
Massey University
Address
Private Bag 102904
North Shore Mail Centre
Auckland 0745
Country
New Zealand
Secondary sponsor category [1] 283367 0
None
Name [1] 283367 0
Address [1] 283367 0
Country [1] 283367 0

Ethics approval
Ethics application status
Not yet submitted
Ethics committee name [1] 286422 0
Health and Disability Ethics Committee - Northern Y
Ethics committee address [1] 286422 0
Ethics committee country [1] 286422 0
Date submitted for ethics approval [1] 286422 0
17/01/2012
Approval date [1] 286422 0
Ethics approval number [1] 286422 0

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 33580 0
Address 33580 0
Country 33580 0
Phone 33580 0
Fax 33580 0
Email 33580 0
Contact person for public queries
Name 16827 0
Dr Pamela von Hurst
Address 16827 0
Institute of Food, Nutrition and Human Health
Massey University
B27 Eastbourne Road,
Albany, Auckland 0632
Country 16827 0
New Zealand
Phone 16827 0
+64 9 414 0800 ext 41205
Fax 16827 0
+64 9 443 9640
Email 16827 0
p.r.vonhurst@massey.ac.nz
Contact person for scientific queries
Name 7755 0
Dr Pamela von Hurst
Address 7755 0
Institute of Food, Nutrition and Human Health
Massey University
Private Bag 102904
Albany, Auckland 0745
Country 7755 0
New Zealand
Phone 7755 0
+64 9 414 0800 ext 41205
Fax 7755 0
+64 9 443 9640
Email 7755 0
p.r.vonhurst@massey.ac.nz

No information has been provided regarding IPD availability


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

Documents added manually
No documents have been uploaded by study researchers.

Documents added automatically
No additional documents have been identified.