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Effect of Nutrition and Wellness Program on Health Parameter Among Employees

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

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07031726
Acronym
WNWP
Enrollment
98
Registered
2025-06-22
Start date
2025-06-12
Completion date
2025-11-30
Last updated
2026-01-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Body Composition, Nutrition, Obesity Prevention, Wellness Program, Workplace Interventions

Keywords

worksite wellness program, obesity prevention, personalized physical activity, personalized nutrition, employee health

Brief summary

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.

Detailed description

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.

Interventions

BEHAVIORALWorksite Nutrition and Wellness Program

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

BEHAVIORALStandard education

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

Sponsors

University of Brawijaya
Lead SponsorOTHER
Universiti Putra Malaysia
CollaboratorOTHER
Universiti Teknologi MARA (UiTM) Sungai Buloh Campus, Malaysia
CollaboratorUNKNOWN

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Masking description

Participants were blinded to group assignment to reduce bias in self-reported outcomes and compliance. Investigators and outcome assessors were not blinded due to the nature of the intervention

Intervention model description

Participants will be assigned to different groups based on faculty divisions using a cluster allocation model. Each group will receive either a structured wellness program or usual care.

Eligibility

Sex/Gender
ALL
Age
20 Years to 40 Years
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
Change in Body Mass Index (BMI)Baseline, Week 6, and Week 12Change in BMI measured using standard anthropometric protocol

Secondary

MeasureTime frameDescription
Change in Hand Grip StrengthBaseline, Week 6, and Week 12Measured using a digital dynamometer (dominant hand).
Body Fat PercentageAt Baseline, Week 6, and Week 12% Body fat in percentage measured via bioelectrical impedance analysis (BIA).
Skeletal massBaseline, week 6, Week 12Skeletal mass in percentage using BIA.
Change in VO₂ MaxBaseline, Week 6, and Week 12Estimated VO₂ Max via submaximal aerobic capacity test (e.g., Rockport or Queens step test).
Change in Fasting Blood GlucoseBaseline and Week 12Measured using capillary blood sample with a point-of-care glucometer (EasyTouch®) after ≥8 hours fasting.
Change in Waist CircumferenceBaseline, Week 6, Week 12Waist measured in centimeters at midpoint between lowest rib and iliac crest.
Change in Total Blood CholesterolBaseline and Week 12Total cholesterol measured using capillary blood with a point-of-care cholesterol meter (EasyTouch®).

Countries

Indonesia

Contacts

PRINCIPAL_INVESTIGATORIrka Dwi Fatmawati, S.Tr. Gz.

University of Brawijaya

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026