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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT00315770
Other study ID # FQS-506359
Secondary ID
Status Active, not recruiting
Phase Phase 1
First received
Last updated
Start date January 2004
Est. completion date April 2020

Study information

Verified date August 2018
Source Landspitali University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a controlled, randomized, intervention trial (CRIT) with 20-40 year old overweight individuals (n = 320) across Europe in order to distinguish between biologically active components of seafood, i.e., seafood proteins and n-3 lipids, regarding their effects on risk factors for metabolic syndrome, bone health, and weight management.


Description:

Subjects were recruited through advertisements from October 2004 until April 2005. Recruitment of 320 subjects (140 from Iceland, 120 from Spain, and 60 from Ireland). The inclusion criteria were body mass index (BMI) 27.5 to 32.5 kg/m2, age 20-40 years, and a waist circumference of equal or more than 94 cm and 80 cm for men and women, respectively. Exclusion criteria were weight change due to weight loss diet within 3 months before the start of the study, use of supplements giving n-3 fatty acids, calcium or vitamin-D during the last three months, drug treatment of diabetes mellitus, hypertension or hyperlipidemia and women's pregnancy or lactation. Each subject was instructed to follow a diet, energy-restricted by 30% from estimated energy expenditure (approximately 600 kcal/day), for 8 consecutive weeks. The subjects were randomly assigned to four diets varying in types of dietary protein and amount of n-3 fatty acids (especially very long chain n-3 fatty acids):

I: no seafood (control, including 6 placebo capsules/day)

II: lean fish (150 g cod x 3/week)

III: fatty fish (150 g salmon x 3/week)

IV: fish-oil capsules (6 capsules/day)

Risk factors for metabolic syndrome, bone health and weight management were analysed at baseline and endpoint.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 320
Est. completion date April 2020
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria:

- Body mass index (BMI) of 27.5 to 32.5 kg/m2

- Ages 20-40 years

- Waist circumference of equal or more than 94 cm and 80 cm for men and women, respectively

Exclusion Criteria:

- Weight change due to weight loss diet within 3 months before the start of the study

- Use of supplements giving n-3 fatty acids

- Calcium or vitamin D during the last three months

- Drug treatment for diabetes mellitus

- Hypertension or hyperlipidemia

- Women's pregnancy or lactation

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
weight loss diets for young adults


Locations

Country Name City State
n/a

Sponsors (6)

Lead Sponsor Collaborator
Landspitali University Hospital European Commission, The National Research Institute on Agriculture and Fisheries Research, Lisbon, Portugal, University College Cork, University of Iceland, University of Navarra

Outcome

Type Measure Description Time frame Safety issue
Primary Weight loss
Primary Anthropometry
Secondary Blood lipid profile (total high-density lipoprotein [HDL]- and low-density lipoprotein (LDL)-cholesterol, triacylglycerol)
Secondary Fatty acid composition of red blood cells
Secondary Fasting plasma glucose and fasting insulin
Secondary C-reactive protein
Secondary Prostaglandins
Secondary Interleukins
Secondary Intercellular adhesion molecules
Secondary Vascular cell adhesion molecules
Secondary Antioxidants/pro-oxidants
Secondary Serum ghrelin
Secondary Leptin
Secondary Quantitative insulin-sensitivity check index (QUICKI)
Secondary Adiponectin
Secondary Plasminogen activator inhibitor (PAI-1)
Secondary Cortisol
Secondary Glutathione (GSH) reductase
Secondary Malondialdehyde
Secondary Bone specific alkaline phosphatase
Secondary Osteocalcin
Secondary Parathyroid hormone (PTH)
Secondary 25-hydroxyvitamin D3 [25(OH) D3]
Secondary Creatinine
Secondary Pyridinoline (Pyr) and deoxypyridinoline (Dpyr)
Secondary Visual analogue scale for satiety
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