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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04601025
Other study ID # CL10840098
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 28, 2019
Est. completion date October 10, 2019

Study information

Verified date October 2020
Source Kutahya Medical Sciences University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study was carried out once a week on the same day and for three-week duration, with total of 17 randomly selected participants with ages between 18 and 24 years. The test foods containing different vegetable fiber sources (chickpeas and oats) were given to the participants every week as isocaloric, which have been the control food for a week. The satiety status was evaluated by visual analog scale (VAS) for total of five times as immediately before the test food consumption and at 30, 60, 90 and 120 minutes after consumption. Fasting and postprandial blood glucose levels were measured. A 24-hour retrospective food consumption record was obtained the next day.


Recruitment information / eligibility

Status Completed
Enrollment 17
Est. completion date October 10, 2019
Est. primary completion date June 24, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 25 Years
Eligibility Inclusion Criteria: - Age range of 18-24 years, - Studying at the university, - Not smoking, - Having normal BMI according to the World Health Organization (18.5-24.9 kg / m2), - Satisfy blood donation criteria, - Along with not suffering from diabetes, - Abnormal thyroid problem, - Gastrointestinal disorder, - Food allergy or intolerance Exclusion Criteria: - Individuals who smoke, - Follow a special diet program, - Having eating disorder, - Vegan or vegetarian, - Do not consume legumes, - Having gluten or lactose intolerance, - Suffering from a chronic disease, - Pregnant or breastfeeding

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Yoghurt
200 ml plain full-fat yoghurt
Chickpea+Yoghurt
80 ml plain full-fat yoghurt + 70 gr cooked chickpea
Oat+Yoghurt
80 ml plain full-fat yoghurt + 100 gr cooked oat

Locations

Country Name City State
Turkey Medipol University Istanbul

Sponsors (2)

Lead Sponsor Collaborator
Kutahya Medical Sciences University Medipol University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change of Satiety Appetite will be examined using visual analog scale (0-10) with five questions: 0 least and 10 greatest 0, 30, 60, 90 and 120 minutes after test food consumption
Primary Baseline and postprandial blood glucose concentration Blood glucose concentration before and at the end of 120.minutes after test food intake Up to 120. minutes
Primary Ad libitum lunch intake Quantification of lunch intake after the 120 minutes of test food consumption End of the 120.minutes
Secondary Quantification of food intake during the rest of the day 24-hours food consumption record from the end of the ad libitum lunch until the next day 9.00 AM. During the 24-hours of experimental day.
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