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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02399280
Other study ID # ND-106
Secondary ID
Status Completed
Phase N/A
First received March 22, 2015
Last updated April 3, 2017
Start date February 2015
Est. completion date August 2015

Study information

Verified date April 2017
Source Novindiet Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of the present study is to evaluate the effect of consuming higher caloric intake at lunch in contrast to dinner on weight loss of obese and overweight female adults when they are in a multidisciplinary weight loss plan .


Recruitment information / eligibility

Status Completed
Enrollment 70
Est. completion date August 2015
Est. primary completion date June 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria:

- Must have Body mass index (BMI) between 27-35 kg/ m².

- Must be able to have moderate exercise.

- Must be interested to have weight loss.

Exclusion Criteria:

- Participating in a research project involving weight loss or physical activity in the previous six months.

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

- Taking medication 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:
Lunch as main meal(LM)+ Diet
Subjects are asked to have high caloric intake at lunch and low caloric intake at dinner, while they are on a multidisciplinary weight loss plan for 12 weeks.
Dinner as main meal(DM)+ Diet
Subjects are asked to have high caloric intake at dinner and low caloric intake at lunch, while they are on a multidisciplinary weight loss plan for 12 weeks.

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 12 weeks
Secondary waist circumference 12 weeks
Secondary Fasting plasma glucose level 12 weeks
Secondary Lipid profiles 12 weeks
Secondary Insulin resistance(HOMA) 12 weeks
Secondary Body mass index 12 weeks
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