The Impact of Treadmills and Cooler Environments for Office Workplaces on Ergonomics, Heating Energy Requirements, Performance, as Well as Back and Cardiometabolic Health
ELBEngLück
Einfluss Von Laufbändern für Büroarbeitsplätze Auf Ergonomie, Heizenergiebedarf, Leistungsfähigkeit Sowie Rücken- Und Kardiometabolische Gesundheit
1 other identifier
interventional
16
1 country
1
Brief Summary
The aim of the project is to gain insights into the effects of treadmills at a standing desk and reduced room temperature on back and cardiometabolic health, cognitive performance, thermal comfort, and the associated heating energy requirements of buildings. Healthy young men and women will spend four consecutive days in a controlled laboratory office environment after a baseline visit. During the baseline visit, volunteers are familiarized with the treadmill and start wearing a continuous glucose monitor. The four consecutive laboratory office days are each scheduled from 8:30AM to 04:30PM. In a randomized order, participants the first two office days either at 19°C or 23°C room temperature. The first office day of each temperature conditions is spent only sedentary, while for the second one is regularly interrupted with light walking on the treadmill. Otherwise, the daily routine and test battery will be exactly the same between days, including a standardized breakfast and lunch meal, an attention task in the morning, and frequent subjective thermal comfort ratings and blood pressure measurements. Interstitial glucose as well as heart rate and heart rate variability will be continuously monitored through wearable devices. Treadmill walking will be videorecorded.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Jul 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 3, 2025
CompletedFirst Submitted
Initial submission to the registry
August 11, 2025
CompletedFirst Posted
Study publicly available on registry
August 24, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 31, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
August 31, 2025
CompletedDecember 16, 2025
December 1, 2025
2 months
August 11, 2025
December 15, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
Subjective thermal comfort rating
At regular intervals over each of the four laboratory office days
Interstitial glucose levels
Interstitial glucose levels measured by continuous glucose monitors
Continuously sampled every 15 min over all four laboratory office days
Working memory assessed by the TAP (Zimmermann & Fimm, 2002) n-back task
Participants view sequences of numbers and indicate whether the current number matches one presented one or two steps earlier. Outcome variables are accuracy (% correct) and reaction time (ms).
10:00-11:00 AM during each of the four laboratory office days
Divided attention assessed by the TAP (Zimmermann & Fimm, 2002) divided attention task
Participants simultaneously perform a visual and an auditory discrimination task. Outcome variables are reaction time (ms) and error rates.
10:00-11:00 AM during each of the four laboratory office days
Secondary Outcomes (10)
Systolic and diastolic blood pressure
at 09:00, 11:00, 12:30, 14:30 and 16:00 over all four laboratory office days
Heart rate
continuously from 08:30AM to 04:30PM over all four laboratory office days
Heart rate variability
continuously from 08:30AM to 04:30PM over all four laboratory office days
Skin temperature
continuously from 08:30AM to 04:30PM over all four laboratory office days
Cognitive flexibility assessed by the TAP (Zimmermann & Fimm, 2002) task-switching module
10:00-11:00 AM during each of the four laboratory office days
- +5 more secondary outcomes
Study Arms (4)
Sedentary activity at standard room temperature (23°C)
EXPERIMENTALSedentary activity at standard room temperature (23°C)
Walking activity at standard room temperature (23°C)
EXPERIMENTALWalking activity at standard room temperature (23°C)
Sedentary activity at lowered room temperature (19°C)
EXPERIMENTALSedentary activity at lowered room temperature (19°C)
Walking activity at lowered room temperature (19°C)
EXPERIMENTALWalking activity at lowered room temperature (19°C)
Interventions
The office is day is spent in 19 or 23°C room temperature from 08:30AM to 04:30PM.
From 08:30AM to 04:30PM, the office is day is spent either fully sedentary or interspersed with light walking on a treadmill (60 min at 10:00AM, 15 min at 01:00PM, 15 min at 02:00PM, 15 min at 03:00PM, 15 min at 04:00PM).
Eligibility Criteria
You may qualify if:
- Physically active, healthy test subjects
- Participants who are able to understand the research project
- Adult test volunteers (aged \>18 and \<40)
- German language skills at B2-C2 level
You may not qualify if:
- An implanted pacemaker
- Participants who are unable to give consent/participants with a legal representative
- Age under 18 or over 40
- Pregnant participants
- Participants with a BMI \>28
- Participants with underlying diseases with significant functional limitations (e.g., rheumatoid arthritis, diabetes mellitus, high blood pressure)
- Reading and/or spelling disorders or combined disorders of scholastic skills (ICD-10 F81.0 - F81.3)
- Participants with a possible SARS-CoV-2 infection will be excluded from the study for the duration of the infection
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University hospital at RWTH Aachen
Aachen, 52074, Germany
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Jan-Frieder Harmsen, PhD
RWTH Aachen University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
August 11, 2025
First Posted
August 24, 2025
Study Start
July 3, 2025
Primary Completion
August 31, 2025
Study Completion
August 31, 2025
Last Updated
December 16, 2025
Record last verified: 2025-12
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL
- Time Frame
- The study protocol is available from the 11th of August 2025 onwards for at least 5 years.
- Access Criteria
- The study protocol can be requested via email to study officials.
The study protocol can be requested via email to study officials.