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Completed

NCT Number: NCT07031726

Effect of Nutrition and Wellness Program on Health Parameter Among Employees

This study aims to evaluate the effectiveness of a worksite-based nutrition and wellness program in improving body composition, metabolic profile, and physical fitness among university employees who are overweight or obese. The intervention includes personalized and structured physical activity (brisk walking), nutritional education, and self-monitoring using mobile applications. Participants will be assessed at baseline, after 6 weeks and 12 weeks of intervention to determine changes in fat mass, muscle mass, waist circumference, and related health indicators. This program is designed to promote healthier lifestyle habits and prevent non-communicable diseases in the workplace.

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Key information

Age range

20 year–40 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Universitas Brawijaya - Kampus 2

Malang, East Java, 65145, Indonesia

About this study

This study is cluster randomized controlled trial conducted at Universitas Brawijaya to assess the effectiveness of a comprehensive workplace-based wellness intervention. The intervention comprises three key components: (1) structured physical activity is brisk walking with 150 minutes minimum for target per week; (2) personalized nutrition education delivered through interactive counseling; and (3) daily self-monitoring using a mobile application.

Participants include university employees categorized as overweight or obese, who work in sedentary office jobs for more than 5 hours per day. Subjects will be assessed at three time points-baseline, after 6 weeks, and after 12 weeks-to measure changes in body composition (e.g., body mass index, body fat percentage, subcutaneous fat, skeletal mass, and waist circumference), metabolic profile (e.g., fasting blood glucose and cholesterol), and physical fitness parameters.

The study aims to provide evidence on the impact of structured, low-cost wellness programs in reducing obesity-related health risks among adult employees in institutional settings. Ethical approval has been obtained from the Faculty of health, Universitas Brawijaya. The results are expected to support future implementation of health promotion policies in the workplace.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Employees aged 20-40 years
  • BMI ≥ 23 kg/m²
  • Body fat percentage ≥ 25% as measured by body composition analysis
  • Employed in white-collar occupations with predominantly sedentary work activities, defined as sitting for ≥ 5 hours per day, based on results from the Global Physical Activity Questionnaire (GPAQ).
  • Not engaging in regular vigorous physical activity, defined as participating in such activity less than 3 times per week, according to GPAQ results.
  • Not having a medical condition that could inhibit participation in the intervention.
  • Be willing to attend the program for a full 12 weeks.

Exclusion criteria

  • A history of severe chronic disease, including type 1 diabetes, severe coronary heart disease, or kidney failure.
  • Be enrolled in other weight loss programs that may affect the results of the study.
  • Regular engagement in vigorous-intensity exercise prior to the start of the intervention program.
  • Not classified as a white-collar sedentary worker based on the Global Physical Activity Questionnaire (GPAQ) assessment.

Treatment and study plan

Worksite Nutrition and Wellness Program

Behavioral

A structured behavioral intervention combining personalized physical activity and structured physical activity (Zumba classes), personalized nutrition counseling, and mobile app-based self-monitoring.

Other names: WNWP, personalized physical activity, personalized nutrition

standard education

Behavioral

General educational materials on healthy eating and physical activity based on the Ministry of Health guidelines. No tailored or active intervention provided.

Primary outcomes

  1. Change in Body Mass Index (BMI)

    Time frame: Baseline, Week 6, and Week 12

    Change in BMI measured using standard anthropometric protocol

Secondary outcomes

  1. Body Fat Percentage

    Time frame: At Baseline, Week 6, and Week 12

    % Body fat in percentage measured via bioelectrical impedance analysis (BIA).

  2. Skeletal mass

    Time frame: Baseline, week 6, Week 12

    Skeletal mass in percentage using BIA.

  3. Change in Waist Circumference

    Time frame: Baseline, Week 6, Week 12

    Waist measured in centimeters at midpoint between lowest rib and iliac crest.

  4. Change in Hand Grip Strength

    Time frame: Baseline, Week 6, and Week 12

    Measured using a digital dynamometer (dominant hand).

  5. Change in VO₂ Max

    Time frame: Baseline, Week 6, and Week 12

    Estimated VO₂ Max via submaximal aerobic capacity test (e.g., Rockport or Queens step test).

  6. Change in Fasting Blood Glucose

    Time frame: Baseline and Week 12

    Measured using capillary blood sample with a point-of-care glucometer (EasyTouch®) after ≥8 hours fasting.

  7. Change in Total Blood Cholesterol

    Time frame: Baseline and Week 12

    Total cholesterol measured using capillary blood with a point-of-care cholesterol meter (EasyTouch®).

Sponsors and collaborators

Lead sponsor

University of Brawijaya

Other

Collaborators

  • Universiti Putra Malaysia
  • Universiti Teknologi MARA (UiTM) Sungai Buloh Campus, Malaysia

Registry information

Official study title

The Effectiveness of Worksite Nutrition and Wellness Program on Changes in Body Composition, Metabolic Profile, and Physical Fitness Among Employees

Acronym: WNWP

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Jun 22, 2025
Registry last updated
Jan 28, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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