A Detailed Protocol for Perspiration Monitoring Using a Novel, Small, Wireless Device


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Recently, we developed a small wireless device for perspiration monitoring. In this article, we present detailed protocols on how to use the device for perspiration monitoring with an example of the sympathetic activity test.

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Ogai, K., Fukuoka, M., Kitamura, K. i., Uchide, K., Nemoto, T. A Detailed Protocol for Perspiration Monitoring Using a Novel, Small, Wireless Device. J. Vis. Exp. (117), e54837, doi:10.3791/54837 (2016).


Perspiration monitoring can be utilized for the detection of certain diseases, such as thermoregulation and mental disorders, particularly when the patients are unaware of such disorders or are having difficulty expressing their symptoms. Until now, several devices for perspiration monitoring have been developed; however, such devices tend to have a relatively large exterior, considerable power consumption, and/or less sensitivity.

Recently, we developed a small, wireless device for perspiration monitoring. The device consists of a temperature/relative humidity (T/RH) sensor, battery-driven small data logger, and silica gel as a desiccant in a small cylindrical exterior. The T/RH sensor is placed between the detection windows (through which the water vapor from the skin enters) and the silica gel. The underlying principle of the perspiration monitoring device is based on Fick's law of diffusion, which means that water vapor flux from the skin to the silica gel (i.e. transepidermal water loss and perspiration) can be captured by change in humidity at the T/RH sensor. In addition, a baseline subtraction method was adopted to distinguish perspiration and transepidermal water loss.

As shown in the previous report, the developed device can monitor the perspiration at any sites of the body in an easy, wireless manner. However, detailed methods of how to use the device have not been disclosed yet. In this article, therefore, we would like to show the point-by-point tutorials of how to use the device for perspiration monitoring, by showing the sympathetic activity test with the sympathetic skin response monitoring as an example.


Human perspiration, generally known as "sweating," is not just a mechanism for thermoregulation1, but it is also related to certain kinds of diseases. The etiology of abnormal perspiration is broad, including: heatstroke, hyper- or hypothyroidism2, brain infarction3, diabetes mellitus4, dysautonomia5, menopause (known as "hot flash")6, cystic fibrosis7, Parkinson's disease8, and social anxiety disorder9. In light of the number of perspiration-related diseases, it has been considered beneficial to monitor perspiration rates for the early diagnosis or prediction of such diseases (e.g., prevention of heatstroke) in a ubiquitous manner10.

To date, only a small number of devices for perspiration monitoring have been proposed. In early days, skin conductance and relative humidity were used for indirect indices of the amount of perspiration11,12. Most recently, several kinds of flexible, wearable sensors for perspiration monitoring have been proposed13-19, although they are intended for the analysis of sweat electrolytes rather than the amount or temporal pattern of perspiration. The calculation of water vapor diffusion has been utilized for a more quantitative method of monitoring water exchange from the skin20-23. However, this requires (1) the assumption that the outer atmosphere is still and constant20, (2) enough sensitivity to detect the natural flow of water vapor21,22, or (3) a coolant (e.g., Peltier device that consumes a substantial amount of electricity) to condense water vapor to liquid23; thus, they might be difficult for daily and long-term monitoring. As an alternative, a ventilated chamber method was developed20,24,25. In the ventilated chamber method, dry nitrogen or dehumidified air is infiltrated in a small chamber adjacent to the skin from a nitrogen gas tank or a pump, and gas in the water vapor evaporated from the skin is collected. The amount of water vapor from the skin can be calculated from the difference of the humidity in the outlet and inlet gases. Although this method can estimate the amount of perspiration very precisely, a nitrogen gas tank or a mechanical pump is generally large enough to impede daily monitoring.

To address these drawbacks, we have recently developed a novel device for perspiration monitoring, in which a closed chamber with a desiccant-driven enforced water vapor flow, enabled sensitive and long-term monitoring26. This device consists of a cylindrical plastic exterior, temperature/relative humidity (T/RH) sensor with recording microprocessor, and silica gel (Figure 1). In principle, the outer atmosphere should not interfere with the water vapor flow, and a coolant or ventilating chamber is not required. Perspiration profiles can be obtained by solving equations using a spreadsheet software26. A previous study has only shown the principle of the developed device and has omitted the detailed method for how to use the device because of space limitations.

The objective of this article, therefore, is to show a detailed method of how to use the developed device for perspiration monitoring, by showing the recording of stress-induced palmar perspiration during the sympathetic activity test as an example.

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NOTE: The device, including the method of analysis, is covered by Japanese Unexamined Patent Application Publication No. 2011-169881 and the Japanese Patent No. 5708911. This study, including the protocol of the experiment with human subjects, was approved by the Medical Ethics Committee of Kanazawa University (#553-1).

1. Prerequisites for the Perspiration Monitoring Device

NOTE: Perform these steps only once before the first use.

  1. Install the universal serial bus (USB)-serial port conversion interface drivers in the computer27. If the drivers are already installed, skip this step.
  2. Connect the USB-serial port conversion interface to the computer via USB cable. Wait for the automatic driver installation if any.
  3. Set the parameters of the conversion interface and check the ID number of the serial port as follows.
    1. Open the device manager, and select [View] → [Devices by Type].
    2. Locate the "Ports (COM & LPT)" heading, and expand the section to find the heading containing "CP210x USB to UART Bridge" in the list.
    3. Memorize the ID number of the port (e.g., "COM5") in the "CP210x USB to UART Bridge" heading.
    4. Double click the "CP210x USB to UART Bridge," and open the "Port Settings" tab.
    5. Set the parameters as follows: "Bits per second" = 9600, "Data bits" = 8, "Parity" = "None," "Stop bits" = 1, and "Flow control" = "None."
    6. Click the "OK" button to close the window, and close the device manager.

2. Setup of the Perspiration Monitoring Device

NOTE: Set the recording settings as follows before using the device. Repeat these steps for each device if multiple devices are to be used.

  1. Make sure the battery is not inserted in the perspiration monitoring device.
  2. Plug the white connector of the USB-serial port conversion interface to the receptacle at the top of the perspiration monitoring device.
  3. Execute the perspiration recording software, followed by setting the device parameters as follows.
    1. Open the "Settings" tab.
    2. Set the "COM" number to the ID number of the serial port (see step 1.3.3).
    3. Click the "Confirm Connection" button. Check if the message "Connected…" appears.
    4. At the "Data File Folder" settings, choose the drive and select the folder where the perspiration data will be saved. To select the subfolder, double click the folder to open.
    5. Set the "Number of holes" to "4."
  4. Open the "Measure & Rec" tab, and set the "Time Interval" to the desired sample time.
  5. Insert a battery to the perspiration monitoring device.
  6. Fill the device with dry silica gel (color should be blue or green if the color indicator is available), and close the lid. If the lid does not close completely, reduce the amount of silica gel.
  7. Click the "Start Logging Now" button in the perspiration recording software.
    NOTE: Because the perspiration recording starts just after the disconnection, the perspiration monitoring device may be left connected until the monitoring is to be started.

3. Setup for the Measurement of Sympathetic Skin Response (SSR)

NOTE: These steps are intended to monitor the sympathetic activities as the palmar SSR, and are not necessarily required for perspiration monitoring itself. SSR is a change of skin potential according to the sympathetic arousal stimulation such as upset and concentration28,29.

  1. Cleanse the skin where the SSR is to be recorded with an alcohol swab.
  2. Put the anode, cathode, and grounding electrode on the palm, back of the hand, and wrist, respectively, by means of an electrode paste. Fix the electrodes with medical tape.
  3. Set the conditions of the instrumentation amplifier by turning the corresponding knobs of the amplifier as follows: Sensitivity = 1 mV/V, High cut filter ("HI CUT") = 3 kHz, and Low cut filter ("LO CUT") = 0.5 Hz.
  4. Execute the SSR recording software, and start the recording at a sampling rate of 200 Hz by clicking the "Start Measurement" button in the software.

4. Recording of the Perspiration

  1. Put a medical double-sided tape on the bottom of the perspiration monitoring device. When putting a tape, make sure the measurement windows (i.e. four holes at the bottom of the device) are not obstructed.
  2. Disconnect the perspiration monitoring device from the USB-serial port conversion interface. Immediately after the disconnection, observe the perspiration monitoring begin automatically. Make sure the LED lamp is blinking.
  3. Remove the release liner of the medical double-sided tape, and put the perspiration monitoring device on the skin where perspiration is to be monitored.
  4. Wait 10 min for stabilization of water vapor diffusion.
    NOTE: Although this process cannot be monitored, the previous study has confirmed that waiting 10 min is sufficient for stable monitoring26.
  5. Start the examination (e.g., sympathetic activity test).
  6. After the examination, remove the perspiration monitoring device from the skin. To stop the SSR recording, click the "Stop Measurement" button in the SSR recording software, and remove all electrodes from the skin.

5. Perspiration Analysis

  1. Connect the perspiration monitoring device to the USB-serial port conversion interface (as in step 2.2).
  2. Execute the perspiration monitoring software.
  3. Open the "Settings" tab, and click the "Confirm Connection" button.
  4. Open the "Measure & Rec" tab, and click the "Download" button to save the raw data of the device in the specified folder (see step 2.3.4).
  5. Perform perspiration analysis as follows.
    1. Open the "Analysis" tab, and click the "Read Data File." Observe the "Open File" dialog pop up. Select the saved file in the step 5.4, and then click the "Open" button.
      NOTE: The software automatically performs perspiration analysis based on the published method26, and the results will appear on the screen. At the same time, the perspiration data as the comma-separated values format will be saved in the same folder.

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Representative Results

Using this novel device for perspiration monitoring (Figure 1) and the Fick's law-based calculation, the temporal perspiration profiles can be obtained in an easy, wireless manner. Figure 2 shows representative data of wireless perspiration monitoring during the sympathetic activity test. In the experiment, the device for the perspiration monitoring, along with the electrodes for the sympathetic skin response (SSR) monitoring, was attached to the subject's palm. For the sympathetic activity test, the subject was requested to sit and perform the following tasks: (1) take a deep inspiration 5 times with 1 min intervals, and (2) do a mental calculation (e.g., continuously subtract 7 from 100, or the "Flash Anzan" in which the participant sums up the number displayed one after the other on a computer screen) to evoke sympathetic activity. The perspiration and the SSR were simultaneously recorded during the stress conditions. As a result of deep inspiration and mental calculation, the sympathetic activity-induced palmar perspiration could be measured using the developed device. Figure 3 shows representative data of multipoint measurement during daily activities. About 1 hr recording of perspiration at the palm (emotional sweating) and the anterior chest (thermal sweating) showed distinct patterns according to the activities.

Figure 1
Figure 1: The Novel Device for Perspiration Monitoring. (A) The exterior of the device containing dry silica gel. (B, C) A "doughnut-shaped" double-sided tape used in this study and its attachment to the device. (D) Attachment of the device to the skin. Please click here to view a larger version of this figure.

Figure 2
Figure 2: Representative Recording of Perspiration Under the Sympathetic Activity Test. (A) Attachment of the perspiration monitoring device with the sympathetic skin response (SSR) electrodes on the palm. (B) As a result of sympathetic activity test, palmar perspiration along with the SSR reaction was observed in response to the sympathetic activities. Please click here to view a larger version of this figure.

Figure 3
Figure 3: Representative Multipoint Recording of Perspiration During the Daily Activities. The distinct patterns of perspiration according to the different parts of the body (red line, at the palm; blue line, at the anterior chest) were observed during several activities (e.g., going downstairs, driving a car, having a lunch with talking, and shopping). Please click here to view a larger version of this figure.

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The aim of this article is to introduce the use of a novel, wireless perspiration monitoring device. Owing to the recent progress of engineering, more accurate, easy-to-handle methods for temporal perspiration monitoring have been proposed; the ventilated chamber method24,25 and the vapor pressure diffusion method23 are representative examples. However, the ventilated chamber method requires the use of dry nitrogen or a pump with desiccant to produce a dry atmosphere, and thus, the exterior tends to be large. The vapor pressure diffusion method can be adopted in a small exterior, although the open chamber system can be largely influenced by the outer atmosphere, and the closed chamber system has a problem with either water vapor saturation (the chamber is filled with a saturated water vapor) or considerable power consumption of a water vapor condenser (e.g., Peltier device).

To address the situation, we have recently developed a novel wireless device for perspiration monitoring26. In the device, the water vapor from the skin can be captured by a desiccant, enabling a constant but natural flow. In the course of the water vapor traveling, the T/RH sensor captures the flow of the water vapor as a change in the temperature and relative humidity. By calculating such changes under Fick's law, we could estimate the temporal changes of perspiration amount (mg/cm2/min) with <5% error, relative to the conventional ventilated chamber method26. The developed device can be used, for example, to monitor mental stress (Figure 2), thermal sweating, and ultimately the perspiration-related dysregulation in an easier manner.

The developed device is easy to handle, and so there are few points to consider. However, the perspiration measurement would fail if the silica gel is not dry. Therefore, before the experiment, the examiner should make sure that the silica gel is completely dry (i.e. the color is blue). A previous study has estimated the maximum duration of measurement being longer than 4 hr without changing the silica gel26. To re-nature silica gel, dry it in a drying oven until the color turns blue. A conventional microwave oven is also useful. The perspiration measurement would also fail if the attachment of the device is not sufficient. We recommend the usage of a "doughnut-shaped" double-sided tape.

Nonetheless, the developed device has a limitation. Because of the delicate calculation and the limit of desiccant absorptivity, the error of the amount of perspiration should be considered, especially at the higher level of perspiration. Although we have confirmed the error rate as being <5% relative to the conventional method26, the absolute value of the calculated perspiration value should be handled with caution.

Owing to the small, simple, and wireless design of the device, the multipoint perspiration monitoring under unrestricted conditions can be possible. As shown in Figure 3, the different temporal profiles of perspiration can be detected on the different positions of the skin (i.e. palm and anterior chest) in daily life conditions (e.g., talking, eating foods, driving a car, shopping, etc.). The device, therefore, might be utilized for the simultaneous detection of abnormal sweating derived both from the mental and thermal regulatory system malfunction. For example, the dysregulation of the peripheral nervous system in diabetes might be detected if the unbalanced sweating between the left and right soles were to be detected. We are now planning an observational study of perspiration profiles in hospitalized patients as a clinical experiment.

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The author Fukuoka Masakazu is the president of the Rousette Strategy Inc., where the developed device was assembled. No financial support was received from either Fukuoka Masakazu or the Rousette Strategy Inc.


We would like to acknowledge Mr. Ryohei Suganuma and Ms. Sakie Tachibana who helped perform the research. This study was supported in part by the JSPS KAKENHI Grant Numbers 15K20664, 24500848, and 21500405. This study was also funded in part by the MEXT/JST Tenure Track Promotion Program. A part of this study was based on the Japanese Unexamined Patent Application Publication No. 2011-169881 and the Japanese Patent No. 5708911.


Name Company Catalog Number Comments
Required for perspiration monitoring
Perspiration monitoring device Rousette Strategy Inc. SNT-200
USB-serial port conversion interface Rousette Strategy Inc. UUI-200
Perspiration recording software Rousette Strategy Inc. TED99
Silica gel Wako Pure Chemical Industries Ltd. 194-16665 Type A silica gel should be used.
Medical double-sided tape 3M 2181 Medical grade is recommended because of the attachment to the skin.
Computer Requires Windows operating system.
Name Company Catalog Comments
Required for the monitoring of sympathetic skin response
Instrumentation amplifier Nihon Kohden Corp. AB-611J
Amplifier chassis Nihon Kohden Corp. MEG-6108
Input box Nihon Kohden Corp. JB-610B
Alcohol swab Suzuran Sanitary Goods Co., Ltd. 4545766050846
Electrodes Nihon Kohden Corp. NE-114A
Electrode paste Nihon Kohden Corp. Z-401CE
Medical tape Nichiban Co., Ltd. SG257
Analog signal interface Micro Science K.K. C BOX-014
Analog-to-digital converter Micro Science K.K. ADM-686PCI
SSR recording software Matsuyama Advance Co., Ltd. LaBDAQ2000



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