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

Status

Completed

Intervention / Treatment

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

      • Izola, Slovenia, 6310
        • Faculty of Health Sciences

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
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

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.
180 seconds
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.
180 seconds

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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

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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