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Clinical Trials/NCT00876018
NCT00876018
Completed
Phase 4

A Double Blind Randomized Controlled Trial in School Going Children, to Evaluate the Impact of a Multiple Micronutrient Fortified Nutritional Powder on Physical Performance Measures

GlaxoSmithKline1 site in 1 country300 target enrollmentJuly 7, 2008

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Physical Fitness
Sponsor
GlaxoSmithKline
Enrollment
300
Locations
1
Primary Endpoint
Change From Baseline in Maximal Aerobic Capacity (VO2max)- 12 Inch Step Test After 4 Months
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

The purpose of this study is to evaluate the effect of nutritional supplement on physical performance measures of apparently healthy school going children in India.

Detailed Description

Nutritional status may be important in achieving optimal physical performance. There is evidence of significant improvements in physical fitness, aerobic capacity and anaerobic threshold of children and adolescents with nutritional intervention, albeit in children with initial sub-optimal nutritional status. This may be of particular relevance in developing countries like India, where there is limited data on physical fitness and a wide-spread prevalence of concurrent micronutrient deficiencies even in apparently normal school age children. The present study therefore, is designed to assess the effect of a nutritional supplement on the physical performance measures of school going children. This is a randomized, double blind placebo-controlled study of three treatment groups (1 test, 1 positive control (placebo) and 1 'no intervention') conducted in equal numbers of male or female children \[ages 7-11\] attending day schools in Bangalore. Subjects in the intervention (test and positive control) groups will receive study treatments (fortified or un-fortified nutritional powder) once a day for 4 months. The treatments will be administered under supervision on all school working days; for the weekend and other holidays, sachets will be provided for home consumption. At baseline and 4months, physical performance tests will be administered and blood sample drawn to assess nutritional status. Other selected outcome measures such as nutrition status and muscle strength/ endurance will also be assessed. It is hypothesized that after 4 months of intervention, children consuming fortified nutritional powder will have statistically significant improvements in physical performance/ fitness measures as compared to the two control groups.

Registry
clinicaltrials.gov
Start Date
July 7, 2008
End Date
December 19, 2008
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Boys and girls between ages 7-10.5 years
  • Z score of height for age and weight for age of 0 to \< -3
  • Good general health at screening
  • Understands and is willing, able and likely to comply with all study procedures and restrictions
  • Written informed consent from the parents/ guardians and writtent assent by the study participant

Exclusion Criteria

  • Severe anemia (Hb\<8 g% )
  • Cardiovascular disease on clinical examination or history
  • Any underlying respiratory disease with impairment of lung function
  • Physical disability Children consuming nutritional supplements (tonics, syrups, tablets or chews) and/ or health food drinks on a regular basis
  • Recent history \[3mo\] of serious infections, injuries and/ or surgeries
  • Participation in any nutritional study in the last 1 year
  • Indication that they are likely to move within the period of study intervention
  • Any known food allergies like peanut allergy, gluten allergy
  • Family members of an employee of the Sponsor or the study site.

Outcomes

Primary Outcomes

Change From Baseline in Maximal Aerobic Capacity (VO2max)- 12 Inch Step Test After 4 Months

Time Frame: Baseline, after 4 months

Maximal aerobic capacity (VO2max) is defined as the maximum rate of oxygen consumption, measured during incremental exercise. VO2max was measured with the help of an externally placed 12-inch step test to assess the aerobic fitness/cardio-respiratory endurance of the study participants. In this test, participants were asked to step at 22 steps a minute for 3 minutes. The pulse rate was recorded manually, within 15sec of stopping the test. VO2max was calculated as (VO2 x HRmax) divided by HR observed, where HRmax = 220-Age in years. HRmax= maximum heart rate. VO2 is equal to (0.2 x Stepping Rate) + (2.4 x Step height x Stepping Rate) + 3.5 mL/kg/min. mL/kg/min.= milliliter per kilogram per minute.

Change From Baseline in Time Taken for 40 Meter (m) Sprint After 4 Months

Time Frame: Baseline, after 4 months

A 40m sprint was used to assess speed with time taken to complete the sprint being recorded manually using a digital stopwatch. The moment any part of the designated participant's body reached the marker level, the corresponding examiner stopped their watches and recorded the time for the sprint.

Change From Baseline in Aerobic Capacity-shuttle Test (VO2peak) After 4 Months

Time Frame: Baseline, after 4 months

Aerobic capacity(VO2peak) is defined as maximum rate of oxygen consumption attained on a particular exercise test. VO2peak was measured by 20m shuttle run test to assess aerobic \& whole body endurance. In this test, participants were asked to move around one cone to another placed at 19m distance, reversing direction \& in accordance with a pace dictated by sound signal, that got progressively faster at one minute intervals. The initial pace was set at 4.0 km/hr \& with subsequent increases of 0.5 km/hr every subsequent minute. This test was conducted in groups (of at least 3 children per group). The shuttle was stopped when either the participant chose to stop because of exhaustion or when participant was \> 1m away from cone at 2 consecutive paced signals. The number of shuttles at stoppage was noted. VO2peak was calculated as 31.025 + (3.325 x speed) - (3.248 x age). Speed is speed attained in previous level of shuttle, computed as speed (km/hr) = v + 0.5 x n/60; and age is in years.

Change From Baseline in Visual Reaction Time After 4 Months

Time Frame: Baseline, after 4 months

Visual reaction time was assessed using a customized computer based programme. Participant was provided with a periodic random test visual stimulus among many other 'non test' stimuli. Participant was required to tap the space bar of the computer as fast as possible on the appearance of the test visual stimulus. Three test visual cues were provided at each sitting to allow for training effects. The shortest visual reaction time of the three visual cues was used in analyses.

Secondary Outcomes

  • Change From Baseline in Soluble Transferring Receptors (sTr) After 4 Months(Baseline, after 4 months)
  • Change From Baseline in Maximal Handgrip Strength for Dominant and Non-dominant Hand After 4 Months(Baseline, after 4 months)
  • Change From Baseline in Ferritin Level After 4 Months(Baseline, after 4 months)
  • Change From Baseline in C-reactive Protein Level After 4 Months(Baseline, after 4 months)
  • Change From Baseline in Rate of Decline of Muscle Strength After 4 Months(Baseline, after 4 months)
  • Change From Baseline in Vitamin B2 Level After 4 Months(Baseline, after 4 months)
  • Change From Baseline in Folate Level After 4 Months(Baseline, after 4 months)
  • Change From Baseline in Time to Fatigue After 4 Months(Baseline, after 4 months)
  • Change From Baseline in Hemoglobin Level After 4 Months(Baseline, after 4 months)
  • Change From Baseline in Vitamin B6 Level After 4 Months(Baseline, after 4 months)
  • Change From Baseline in Vitamin B12 Level After 4 Months(Baseline, after 4 months)
  • Change From Baseline in Vitamin C Level After 4 Months(Baseline, after 4 months)

Study Sites (1)

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