MedPath

The Effectiveness of Low Calorie Low Salt Lunch for Weight Reduction of Workers of a Health Promoting Hospital

Not Applicable
Completed
Conditions
Obesity
Overweight
Interventions
Other: Lunch which is calorie-restricted and low-salt
Registration Number
NCT02416544
Lead Sponsor
Seoul National University Hospital
Brief Summary

The aim of this study is to evaluate the effectiveness of Low Calorie Low Salt Lunch for Weight Reduction in overweight or obese workers of a health promoting hospital.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
109
Inclusion Criteria
  • Overweight or obese
  • Hospital workers
Read More
Exclusion Criteria
  • History of major medical problems such as heart disease in the last 6 months
  • Orthopaedic or joint problems that would be a barrier to physical activity
  • Pregnancy
  • Recent weight change of ≥10% of baseline weight
  • Taking medications that might affect body weight
  • Participation in other program about weight control
  • Alcohol or substance abuser
  • Other uncontrolled psychiatric problems
  • Eating disorders
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Two thirds participationLunch which is calorie-restricted and low-saltParticipants in this group starts lunch which is calorie-restricted and low-salt after 4 weeks from the beginning of the study and maintain the diet during 8 weeks.
One thirds participationLunch which is calorie-restricted and low-saltParticipants in this group starts lunch which is calorie-restricted and low-salt after 8 weeks from the beginning of the study and maintain the diet during 4 weeks.
Full participationLunch which is calorie-restricted and low-saltParticipants in this group receive lunch which is calorie-restricted and low-salt during 12 weeks, the total duration of this study.
Primary Outcome Measures
NameTimeMethod
Change from baseline in weight4 weeks, 8 weeks, and 12 weeks

Participants will be monitored for up to 12 weeks after intervention

Secondary Outcome Measures
NameTimeMethod
Change from baseline in waist circumference4 weeks, 8 weeks, and 12 weeks

Participants will be monitored for up to 12 weeks after intervention

Trial Locations

Locations (1)

Seoul National University Bundang Hospital

🇰🇷

Seongnam-si, Gyeonggi-do, Korea, Republic of

© Copyright 2025. All Rights Reserved by MedPath