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Clinical Trials/NCT02399280
NCT02399280CompletedNot Applicable

Effect of High Caloric Intake at Lunch Against Dinner on Weight Loss of Overweight and Obese Women Attending a Weight Loss Program, a Randomized Clinical Trial

Novindiet Clinic2 sites in 2 countries70 target enrollmentStarted: February 1, 2015Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
70
Locations
2
Primary Endpoint
weight loss
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief 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 .

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Participant)

Eligibility Criteria

Ages
18 Years to 45 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

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

Outcomes

Primary Outcomes

weight loss

Time Frame: 12 weeks

Secondary Outcomes

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

Investigators

Sponsor
Novindiet Clinic
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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Effect of High Caloric Intake at Lunch... | Clinical Trial