- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03733366
Thermal Comfort of Different Desktop Materials (Materials)
October 1, 2019 updated by: University of Primorska
Effects of Different Desktop Materials on Thermal Comfort and Attention
The aim of this study is to test the suitability of different types of desk surfaces.
The investigators will test 10 different surfaces (oak-ruff, oak-varnished, oak-oiled, spruce-ruff, spruce-varnished, spruce-oiled, particleboard laminate, particleboard veneer, corian and glass).
Firstly, the investigators will perform tests to assess physical characteristics of the materials (thermal conductivity, hardness, roughness, skid measures).
Secondly, the investigators will measure the participants' forearm skin temperature after 20-minutes of using each desk surface.
During those 20 minutes the participants will solve an attention test.
Study Overview
Detailed Description
People are surrounded by objects that are made of different materials.
These materials should be carefully chosen, especially the ones that are in direct contact with user's skin.
Office workers are constantly in contact with desk surface (while reading, typing, filling in forms, etc.).
Therefore, it is important that the material of desk surface is suitable and properly chosen.
It should be both functional and aesthetic.
The aim of this study is to evaluate the suitability of different desk surfaces for sedentary workers.
The investigators will test 10 different surfaces (oak-ruff, oak-varnished, oak-oiled, spruce-ruff, spruce-varnished, spruce-oiled, particleboard laminate, particleboard veneer, corian and glass).
All surfaces will be square shaped (800x800 mm).
Firstly, the investigators will perform tests to assess physical characteristics of the materials (thermal conductivity, hardness, roughness, skid measures).
Secondly, the investigators will measure the participants' forearm skin temperature after 20-minutes of desk use.
Every participant will test all 10 sample desk surfaces (cross-over design).
The investigators will use thermal IR camera to measure the temperature of participant's skin surface.
The investigators will measure the temperature before and after the contact with desk surface.
During those 20 minutes the participant will solve an attention test to assess the impact of different materials on attention.
At the end, the participants will answer a questionnaire about the suitability of the material.
Study Type
Interventional
Enrollment (Actual)
16
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Izola, Slovenia, 6310
- Faculty of Health Sciences
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 35 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- aged between 18 and 35
Exclusion Criteria:
- pregnancy
- pain presence in any musculoskeletal part > 3 on 10-level scale
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change of the skin temperature measured on forearm
Time Frame: at the beginning and after 20 minutes of using desk surface
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Skin temperature in the forearm will be measured with Infrared thermal camera.
Thermal camera is suitable for the measurements since it is a reliable tool for measuring skin temperature.
The temperature is presented in Celsius degrees.
Moreover, thermal camera provides a thermal picture indicating temperature distribution in the space.
|
at the beginning and after 20 minutes of using desk surface
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Attention test
Time Frame: 180 seconds
|
The attention test will be performed on computer.
On the computer screen letters P and R will appear.
Each time the letter R appears the participant will have to click ''space''.
If a letter P appears the participant should not react.
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180 seconds
|
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Adjusted Mood and feelings questionnaire
Time Frame: 180 seconds
|
The questionnaire consists of two questions.
One is asking the participant about their current mood.
The second question is asking the participant about their current arousal.
The participant answers both questions using a 9-level scale (1 meaning not at all and 9 meaning very much).
There is no total value of the questionnaire.
Also, higher or lower values do not represent better or worse outcome.
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180 seconds
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
November 5, 2018
Primary Completion (Actual)
February 28, 2019
Study Completion (Actual)
April 30, 2019
Study Registration Dates
First Submitted
October 29, 2018
First Submitted That Met QC Criteria
November 5, 2018
First Posted (Actual)
November 7, 2018
Study Record Updates
Last Update Posted (Actual)
October 4, 2019
Last Update Submitted That Met QC Criteria
October 1, 2019
Last Verified
November 1, 2018
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- Thermal comfort
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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