Essential Fatty Acid Deficiency, Lifestyle-related Condition, Overweight and Obesity
Conditions
Keywords
Omega-3, physical activity, children, obesity, sedentary, accelerometry, BMI, fatty acids, inflammatory markers, intervention, randomized, double blind
Brief summary
This study hypothesizes that supplementation of omega-3 fatty acids (OM3) can increase physical activity, inhibit rapid gain in body weight and BMI in both sedentary and normally active 8 year old children. The purpose is secondarily to explore patterns of associations between OM3 supplementation, baseline and follow-up levels in all studied parameters. The study also aims to study if basal levels of OM3 are correlated with physical activity and to study if there is an association between basal levels of OM3 and the effect of OM3 supplementation on physical activity. To study if there is an effect of OM3 supplementation on triglyceride and LDL cholesterol levels and to study if there are more pronounced effects on children with higher levels. To study if OM3 supplementation, compared with placebo reduce weight increase among children at risk to become overweight. To study if there is an association between effects of OM3 on physical activity, weight and risk markers in blood. To study if there are any gender differences.
Interventions
DIETARY_SUPPLEMENTOmega-3
This group will receive capsules containing omega-3, omega-6 and vitamin E. The dosage is six capsules per day containing a total of 558 mg of eico-pentaenoic acid (EPA), 174 mg of docosahexaeonic acid (DHA), 60 mg of gamma-linolenic acid (GLA) and 9,6 mg vitamin E in natural form (alfa-tocopherol), gelatine, glycerol. Participants will be instructed to eat three capsules each morning and evening.
DIETARY_SUPPLEMENTPlacebo
This group will receive capsules containing rape seed oil. Participants will be instructed to eat three capsules each morning and evening.
Sponsors
Midsona AB
Forskningsrådet för arbetsliv och socialvetenskap, FAS
Karolinska Institutet
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
7 Years to 9 Years
Healthy volunteers
Yes
Inclusion criteria
* Children in second grade of Swedish primary school willing to participate
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Total physical activity | 15 weeks | The childrens' physical activity will be monitored during 7 consequtive days at 0 and 15 weeks with tri-axial accelerometer. |
| Body mass | 15 weeks | The childrens' body mass will be measured with standardized scales at 0 and 15 weeks. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Childrens reported quality of life | 15 weeks | A validated questionnaire for self-report of subjective perception of quality of life are filled out by each child at 0 and 15 weeks with assistance of an adult (parent or caregiver). |
| BMI | 15 weeks | The childrens' height will be measured using standardised stadiometer at 0 and 15 weeks. Along with the bosy mass data individual BMI (kilograms/meters squared) will be calculated for each time point. |
| Self reported physical activity | 15 weeks | A validated questionnaire for subjective self-report of physical activity will be filled out by each child at 0 and 15 weeks with assistance by parent or caregiver. |
| Perceived motor skill | 15 weeks | A validated questionnaire for subjective self-report of motor skills are filled out by each child at 0 and 15 weeks with assistance of an adult (parent or caregiver). |
| Cardiovascular risk markers | 15 weeks | Blood samples is collected from all participants at 0 and 15 weeks. This will not be decisive for inclusion in the study. Local anaesthesia will be used and the children can choose not to leave blood. Fasting blood samples will be analyzed for LDL-C, HDL-C, tot-C, TG, hsCRP, TNF-α, IL-6, IL-1, PAI-1, Glucose, Insulin, fatty acids and FTO-gene expression. |
Countries
Sweden
Outcome results
None listed