Skip to main content
Clinical Trials/NCT07440979
NCT07440979
Active, not recruiting
Not Applicable

Effects of Personalized Nutrition Coaching on Body Composition, Dietary Intake, Physical Activity Among Overweight and Obesity Nurses at Indonesian Hospital: A Randomized Control Trial

Fakultas Kedokteran Universitas Padjadjaran1 site in 1 country44 target enrollmentStarted: January 19, 2026Last updated:

Overview

Phase
Not Applicable
Status
Active, not recruiting
Sponsor
Fakultas Kedokteran Universitas Padjadjaran
Enrollment
44
Locations
1
Primary Endpoint
Body weight (BW)

Overview

Brief Summary

Obesity among healthcare workers has become an increasing public health concern, with potential consequences for work productivity, quality of care, and long-term health outcomes. Despite their role in promoting health, healthcare workers often face demanding schedules, high stress levels, and limited access to structured health promotion programs, placing them at elevated risk for overweight and obesity. In the absence of targeted workplace interventions, these conditions may persist and worsen over time, highlighting the need for effective, sustainable, and context-specific strategies to support healthier lifestyles among healthcare workers.

This study aims to assess the effectiveness of personalized nutrition coaching as part of a weight loss program for Nurses in Indonesian Hospital. Participants who receive the intervention are expected to demonstrate improvements in nutritional status, including weight-related outcomes, reduction in body fat percentage, reduction in waist circumference. The intervention is also anticipated to promote healthier dietary intake, characterized by more balanced eating patterns, and higher levels of physical activity. Delivered through individualized online guidance, this program is intended to encourage sustainable lifestyle changes and improve overall health. The study will involve an 8-week intervention conducted among overweight and obese healthcare workers at Dr. Hasan Sadikin General Hospital, Bandung.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Masking Description

Blinding or Masking in behavioral intervention studies is limited and often not fully feasible

Eligibility Criteria

Ages
18 Years to 35 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • A Shift Nurse in Dr. Hasan Sadikin General Hospital Bandung
  • Male and Female, Aged 18-35 years (Young Adult)
  • Overweight (body mass index 23.0-24.99 kg/m²) or obese (body mass index ≥25.0 kg/m²)
  • Willing to participate in the study and provide written informed consent
  • Ownership of a smartphone and access to the internet

Exclusion Criteria

  • Being pregnant and/or breastfeeding.
  • Currently participating in a calorie-restricted diet program
  • Having special conditions such as food allergies, sensitivities, or intolerances, or following a specific dietary pattern (e.g., vegan diet or carbohydrate-restricted diet)
  • Having a recent diagnosis or condition that may interfere with study outcomes (body weight, body fat percentage, waist circumference), such as edema or smoking cessation within the past 3 months
  • Taking medications that may affect the study outcomes
  • Having diseases requiring dietary restriction or specialized Medical Nutrition Therapy (MNT), such as diabetes mellitus, kidney disease, or stroke

Arms & Interventions

Personalized Nutrition Coaching

Experimental

The intervention group consists 22 of Overweight and Obese Healthcare Workers who receive nutrition counseling and personalized nutrition coaching

Intervention: Personalized Nutrition Coaching (Behavioral)

Control

Placebo Comparator

The control group consists of 22 of Overweight and Obese Healthcare Workers who receive nutrition education in the form of a booklet. The booklet provides information on basic balanced nutrition guidelines

Intervention: Control (placebo) group (Other)

Outcomes

Primary Outcomes

Body weight (BW)

Time Frame: 8 weeks

Body mass of the participant measured in kilograms. (i.e., at least 5% of baseline body weight)

Secondary Outcomes

  • Height(8 weeks)
  • Waist circumference (WC)(8 weeks)
  • Body fat percentage(8 weeks)
  • Dietary intake(8 weeks)
  • Physical activity(8 weeks)

Investigators

Sponsor
Fakultas Kedokteran Universitas Padjadjaran
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Tazkiah Syahidah

Department of Public Health, Faculty of Medicine, Universitas Padjadjaran, Indonesia

Fakultas Kedokteran Universitas Padjadjaran

Study Sites (1)

Loading locations...

Similar Trials