The Effectiveness of Low Calorie Low Salt Lunch for Weight Reduction of Workers of a Health Promoting Hospital
Not Applicable
Completed
- Conditions
- ObesityOverweight
- 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
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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
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Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description Two thirds participation Lunch which is calorie-restricted and low-salt Participants 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 participation Lunch which is calorie-restricted and low-salt Participants 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 participation Lunch which is calorie-restricted and low-salt Participants in this group receive lunch which is calorie-restricted and low-salt during 12 weeks, the total duration of this study.
- Primary Outcome Measures
Name Time Method Change from baseline in weight 4 weeks, 8 weeks, and 12 weeks Participants will be monitored for up to 12 weeks after intervention
- Secondary Outcome Measures
Name Time Method Change from baseline in waist circumference 4 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