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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03171948
Other study ID # ND-205
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 10, 2017
Est. completion date January 17, 2019

Study information

Verified date January 2019
Source Novindiet Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to assess the effects of limited portion of almond consumption after a successful weight loss by a comprehensive weight loss plan (NovinDiet Plan) on weight maintenance in obese female adults.


Recruitment information / eligibility

Status Completed
Enrollment 120
Est. completion date January 17, 2019
Est. primary completion date December 12, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria:

- female

- 18-45 years of age.

- Body mass index (BMI) between 23-30 kg/ m² who lost at least 10% of her initial weight by the diet plan.

- Must be able to have moderate exercise.

- Must be interested to keep weight loss.

Exclusion Criteria:

- No Allergy to nut products

- Pregnancy or lactation during the previous 6 months, or planned pregnancy in the next 6 months.

- Taking medications that could affect metabolism or change body weight.

- Report heart problems, chest pain, and cancer within the last five years.

- Smoking

- Menopause

- Diagnosis of any chronic disease such as fatty liver, cancer, chemo/radio therapy, heart disease, immune compromised conditions, abnormal thyroid hormone level.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Almond Group
Almond Group (AG) are asked to have a 30 gr. almond every day in their afternoon snack plus following the hypoenergetic diet
Nut Free group
continue their diet without any nut consumption.

Locations

Country Name City State
Iran, Islamic Republic of NovinDiet Clinic Tehran

Sponsors (3)

Lead Sponsor Collaborator
Novindiet Clinic Tehran University of Medical Sciences, University of Nottingham

Country where clinical trial is conducted

Iran, Islamic Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary weight loss kg 6 Month
Secondary Waist circumference cm 6 Month
Secondary Fasting blood glucose mmol/l 6 Month
Secondary Fasting insulin level mU/l 6 Month
Secondary HbA1c 6 Month
Secondary HOMA-IR percentage (%) 6 Month
Secondary lipid profiles mmol/l 6 Month
Secondary liver function U/l 6 Month
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