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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03341650
Other study ID # SP2
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 2, 2015
Est. completion date December 2017

Study information

Verified date November 2017
Source University of Parma
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To the best of our knowledge, the effect of pasta consumption within a hypocaloric Mediterranean diet has only been scarcely explored yet. Therefore, a two-parallel group dietary intervention was carried out to investigate if pasta consumption could affect the BMI change in obese patients. The primary outcome was the loss of at leat 8% of the initial body weight in the first 6 months. Anthropometric and body composition (from bioelectrical impedance analysis - BIA-) measures were collected every month for the first 6 months and after 1 year. In addition, dietary information was collected at baseline and after 3, 6 and 12 months through a 7-day carbohydrate food record and a 24-h food recall. Blood samples were collected at baseline and at 6 and 12 months to assess: glucose, insulin, Homeostatic model assessment for insulin resistant (HOMA-IR) index, total cholesterol, low-density lipoprotein, high-density lipoprotein, and uric acid. Furthermore, the perceived quality of life was investigated through the 36-items short form health survey (SF36) questionnaire.


Recruitment information / eligibility

Status Completed
Enrollment 44
Est. completion date December 2017
Est. primary completion date December 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 55 Years
Eligibility Inclusion Criteria:

- BMI between 30-45 kg/m2

- healthy subjects

- regular meal consumption

- no celiac disease

- no menopause woman

Exclusion Criteria:

- with a BMI <30 or >45 kg/m2

- having diabetes, hepatic or kidney diseases

- having an eating disorder

- having celiac disease

- menopause woman

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
High Pasta
Participants received a personalised diet program considering their food preferences and eating behaviour, based on the Italian guidelines for a healthy and Mediterranean diet and were encouraged to maintain their habitual consumption of pasta (at least 5 times/week). To encourage participants to prepare healthy meals by using high-quality ingredients, participants were provided with a recipe book and dietary guidelines and recommendations.
Low Pasta
Participants received a personalised diet program considering their food preferences and eating behaviour, based on the Italian guidelines for a healthy and Mediterranean diet and were encouraged to maintain their habitual consumption of pasta (no more than 3 times/week). To encourage participants to prepare healthy meals by using high-quality ingredients, participants were provided with a recipe book and dietary guidelines and recommendations.

Locations

Country Name City State
Italy Department of Food and Drug, University of Parma Parma

Sponsors (1)

Lead Sponsor Collaborator
University of Parma

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change from baseline Body weight at 6 months Measured in kg according to the standard procedure baseline, 6 months
Secondary Change from baseline Body weight at 3 months Measured in kg according to the standard procedure baseline, 3 months
Secondary Change from baseline Body weight at 12 months Measured in kg according to the standard procedure baseline, 12 months
Secondary BMI Calculated as body weight in kilograms divided by the square of the height in meters baseline, 1 month, 2 months, 3 months, 4 months, 5 months, 6 months, 12 months
Secondary Waist circumference Measured in cm according to the standard procedure baseline, 1 month, 2 months, 3 months, 4 months, 5 months, 6 months, 12 months
Secondary Free Fat Mass Estimated by bioelectrical impedance analysis in kg and in % baseline, 3 months, 6 months, 12 months
Secondary Fat Mass Estimated by bioelectrical impedance analysis in kg and in % baseline, 3 months, 6 months, 12 months
Secondary Basal Metabolic Rate Estimated by bioelectrical impedance analysis in kcal/day baseline, 3 months, 6 months, 12 months
Secondary Glucose mg/dL in fasting condition baseline, 6 months, 12 months
Secondary Insulin microU/mL in fasting condition baseline, 6 months, 12 months
Secondary HOMA-IR index calculated from glucose and insulin in fasting condition baseline, 6 months, 12 months
Secondary Total cholesterol mg/dL in fasting condition baseline, 6 months, 12 months
Secondary HDL cholesterol mg/dL in fasting condition baseline, 6 months, 12 months
Secondary LDL cholesterol mg/dL in fasting condition baseline, 6 months, 12 months
Secondary Triglycerides mg/dL in fasting condition baseline, 6 months, 12 months
Secondary Uric Acid mg/dL in fasting condition baseline, 6 months, 12 months
Secondary Energy intake assessed by a 24-h dietary recall as kcal/day baseline, 3 months, 6 months, 12 months
Secondary Nutrient intakes assessed by a 24-h dietary recall as g/day baseline, 3 months, 6 months, 12 months
Secondary Carbohydrate-based food intakes assessed by a 7-day food diary as times/week baseline, 3 months, 6 months, 12 months
Secondary Perceived Quality of Life assessed by the SF36 questionnaire baseline, 3 months, 6 months, 12 months
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