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Workplace Intervention Including Exercise and Nutrition in Obese Office Workers

A Combined Workplace Intervention Including Exercise and Nutrition for Health Promotion in Obese Office Workers: a Randomized Controlled Study

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07603141
Enrollment
36
Registered
2026-05-22
Start date
2023-06-30
Completion date
2024-02-28
Last updated
2026-05-28

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

Conditions

Obesity (BMI>30)

Keywords

occupational setting, wellness, physical activity, functional capacity, dietary habits, hydration

Brief summary

The main objective of this study is to investigate the efficacy of a 6-month workplace combined (exercise and nutrition) intervention in obese office workers, using a randomized controlled study. An additional objective of this study is to evaluate the individual responses per participant following the program.

Interventions

OTHERWorkplace combined (exercise and nutrition) intervention

The IG will participate in a supervised 6-month combined intervention program (exercise and nutrition), which will take place inside the workplace settings during working hours. In more detail, the IG will participate, every working day (5 days/week), in a 6-month supervised combined chair-based exercise program (120 training sessions; 25-40 min/day), including chair based seated and chair-assisted standing exercises to improve flexibility, balance, strength and aerobic capacity. Except exercise, the intervention program consisted of weekly counseling and educational activities in healthy diet and proper hydration using presentations, leaflets, individual and group sessions with nutritionist, use of applications for proper hydration, use of goal-setting cards for healthy options

Sponsors

University of Thessaly
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Sedentary work at least 8 h per day in the office * BMI value ≥ 30 kg/m2 * No chronic diseases (physical or mental) * No use of any medication * No injuries (in lower or upper body) in the last 6 months * No participation in organized exercise programs or nutrition intervention during the last 6 months.

Exclusion criteria

Participants who do not meet the above criteria will be excluded from the study.

Design outcomes

Primary

MeasureTime frameDescription
Body fatBaseline and 6 monthsBody fat (BF): BF% will be assessed using the bioelectrical impedance method (Maltron 900).
Body circumferencesBaseline and 6 monthsThe waist and hip circumferences will be measured using an ergonomic circumference measuring tape (Seca 201).
Blood pressureBaseline and 6 monthsSystolic and diastolic blood pressure will be measured, using an electronic upper arm blood pressure monitor (A\&D-UA-851).
Respiratory functionBaseline and 6 monthsForced vital capacity (FVC) and forced expiratory volume in 1 s (FEV1) will be measured, using a portable spirometer (Micro, Medical, Micro).
Lipidemic profileBaseline and 6 monthsA blood sample will be obtained after overnight fasting (12 h), as previously described \[37\]. Total cholesterol, high-density lipoprotein (HDL) and triglycerides will be determined using a biochemical analyzer (Clinical Chemistry Analyzer Z 1145; Zafiropoulos Diagnostica S.A., Koropi, Greece), and low-density lipoprotein (LDL) will be calculated using the Friedewald equation.
Lower body flexibility:Baseline and 6 monthsThe sit-and-reach test will be performed using a Flex-Tester box (Novel Products Inc., Rockton, IL, USA).
Static balanceBaseline and 6 monthsThe single-limb stance test (with eyes opened) was performed, as previously described by Rinne et al.
Dynamic balance:Baseline and 6 monthsThe timed up-and-go test was performed, as previously described by Rikli and Jones.
Handgrip strengthBaseline and 6 monthsMaximal isometric handgrip strength will be assessed using a portable hydraulic dynamometer (Jamar 5030J1, Horsham, USA).
Aerobic capacity:Baseline and 6 monthsThe YMCA 3 min step test was used, which will be performed following the metronome cadence (96 beats per minute; 4 steps per cycle). The participants' HR will be measured 1 min following the termination of the step test.
Adherence to the Mediterranean dietBaseline and 6 monthsThe adherence to the Mediterranean diet will be assessed before and after the 6-month period using the specific Mediterranean Diet Score (range of total score: 0-55) \[34-35\]. The MedDietScore measures the weekly consumption of the following 9 food groups: non-refined cereals (whole grain bread and pasta, brown rice, etc), fruit, vegetables, legumes, potatoes, fish, red meat and products, poultry, full fat dairy products (like cheese, yoghurt, milk), as well as olive oil and alcohol intake \[35\].

Countries

Greece

Contacts

PRINCIPAL_INVESTIGATORKonstantina Karatrantou

University of Thessaly

PRINCIPAL_INVESTIGATORVassilis Gerodimos

University of Thessaly

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 29, 2026