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Exercise Intervention in Female School Children: Effect on Blood Pressure, Body Mass Index (BMI), and Maths Scores

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ClinicalTrials.gov Identifier: NCT00533819
Recruitment Status : Unknown
Verified October 2008 by Aga Khan University.
Recruitment status was:  Recruiting
First Posted : September 21, 2007
Last Update Posted : October 15, 2008
Sponsor:
Information provided by:
Aga Khan University

September 20, 2007
September 21, 2007
October 15, 2008
September 2007
Not Provided
Blood pressure [ Time Frame: 6 months ]
Same as current
Complete list of historical versions of study NCT00533819 on ClinicalTrials.gov Archive Site
  • Body mass index [ Time Frame: 6 months ]
  • Maths scores [ Time Frame: 6 months ]
Body mass index, Maths Scores [ Time Frame: 6 months ]
Not Provided
Not Provided
 
Exercise Intervention in Female School Children: Effect on Blood Pressure, Body Mass Index (BMI), and Maths Scores
A Phase II Non Randomized Community Intervention Trial in 4 Public Sectors Schools in Karachi. Exercise Intervention in Female School Children: Effect on Blood Pressure, BMI, and Maths Scores
Healthy physical activity decreases blood pressure in young female school children. It also has effects on BMI and maths scores.
  • Primary Objective: To compare the effect of 6 months healthy physical activity on blood pressure in female school children (9-13 yrs) with those who have routine physical activity
  • Secondary objective: To compare the effect of 6 months of healthy physical activity on body mass index and maths scores with those who have routine physical activity
  • Study Design: It would be a non-randomized experimental study (community intervention trial). It is designed to test the effectiveness of exercise on reducing blood pressure and the effect on BMI and maths scores
  • Setting: The study would be conducted in 4 public sector schools in Karachi.
  • Study Population: The study population would be selected from 4 local public sector schools near our hospital, The Aga Khan University Hospital. Two schools would have intervention and 2 schools would serve as controls. Both groups would have a base line screening for the outcome variables and then at 6 months
  • Intervention: The intervention is 30 minutes of healthy physical activity; 4-times/week would be carried out for a period of 6 months. This would be carried out by certified physical trainers who are experts in training children in aerobic exercise. Intervention group will have half an hour session on exercise motivation and its benefits. The routine activity group will have a similar session at baseline.
  • Sampling technique: convenience sampling
  • Sample Size : A sample size of 126 (63 in each arm) achieves 80% power to detect a difference of 4.3 mm in systolic blood pressure between the null hypothesis mean of 110.3 and an alternative hypothesis mean of 105.7 with an estimated standard deviation of 9.7 and with significance level (alpha) of 0.05 using one sided one sample t test. Assuming that there could be a 10% dropout rate we plan to take a total sample size of 140 students. We multiplied the total sample size by 2 to account for the design effect between clusters (schools) and achieved a total sample size of 280 that is 140 in each arm.
  • Dependent variables or outcome variables: Primary outcome measure would be the blood pressure. Secondary outcome measures would be body composition including weight, BMI, central obesity, and maths score. Independent variable would be demographics (age, school class) and the intervention of healthy physical activity and measurement of food intake frequency
Interventional
Phase 2
Allocation: Non-Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Prevention
Hypertension
Other: 6 months of healthy physical activity
half an hour of healthy physical activity including 20 minutes aerobic, 5 minutes warm up and cool down, 4 days a week
  • Experimental: 1
    Intervention: Other: 6 months of healthy physical activity
  • No Intervention: 2
    would have routine physical activity

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Unknown status
280
Same as current
May 2008
Not Provided

Inclusion Criteria:

  • Female children of age 9-11 yrs who are enrolled in the public sector school with a compound facility would be included in the study. Intervention would be offered to those only who will have normal age specific weight in percentiles.

Exclusion Criteria:

  • Those who are suffering from any chronic illness due to they which cannot participate and those who are mentally or physically disabled will be excluded from the study.
Sexes Eligible for Study: Female
9 Years to 11 Years   (Child)
No
Contact information is only displayed when the study is recruiting subjects
Pakistan
 
 
NCT00533819
07GS006CHS
743-CHS/ERC-07
No
Not Provided
Not Provided
Not Provided
Aga Khan University
Not Provided
Principal Investigator: Aysha Almas, MBBS, FCPS Student
Aga Khan University
October 2008

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP