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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03129841
Other study ID # ND-202
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 1, 2017
Est. completion date November 18, 2017

Study information

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

Clinical Trial Summary

The aim of the present study is to test whether late eating dinner could affect the amount of weight loss in healthy obese women in a weight-loss program.


Recruitment information / eligibility

Status Completed
Enrollment 70
Est. completion date November 18, 2017
Est. primary completion date October 5, 2017
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:
Early dinner+Diet
Subjects are asked to eat dinner meals between 7:00- 7:30 PM in the ED group, while they are on a multidisciplinary weight loss plan for 12 weeks.
Late dinner+Diet
Subjects are asked to eat their dinner meal between 10:30-11:00PM, 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 kg 12 Weeks
Secondary waist circumference cm 12 Weeks
Secondary fasting plasma glucose mmol/L 12 Weeks
Secondary insulin level mU/l 12 Weeks
Secondary insulin resistance (HOMA-IR) Score 12 Weeks
Secondary glycosylated hemoglobin (HbA1c) percentage (%) 12 Weeks
Secondary lipid profiles mmol/l 12 Weeks
Secondary Liver Enzyme (SGOT, SGPT) U/l 12 Weeks
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