CClinicalTrials.gg
CompletedNCT07576413Updated May 8, 2026

Effects of Standing Desks and Intermittent Walking on Cognitive Fatigue

An interventional study of Performance of cognitive tasks in Sitting Position, Overexertion From Maintaining Prolonged Standing Position and Walking, sponsored by Clarkson University. Completed at 1 site in United States. Open to participants aged 18 Years to 45 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-05-08.

Sponsored by Clarkson University · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Registered 7 years 11 months after the study started (first participant enrolled Jun 2018, registered May 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
31
Allocation
Randomized
Ages
18 Years to 45 Years
Sex
All
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Study summary

The objective of this randomized-controlled crossover design was to identify inter-individual responses to the use of sitting desks, standing desks and two minutes of walking after twenty-eight minutes of sitting on the performance of cognitive tasks and moods in healthy undergraduate and graduate students. Participants were randomly assigned to an order of interventions and were asked to perform 26 minutes of cognitive tasks followed by completing 2 minutes of surveys where they were asked about their moods. Following the 28 minute cognitive battery participants were given a 2 minute break. In the seated condition participants performed all tasks on a seated desk and had to remain seated for their 2 minute break. In the standing condition participants performed the entire battery standing and had to remain standing for the 2 minute break. In the intermittent walking condition, participants performed all tasks in a seated condition and for their 2 minute break, participants were asked to walk for 2 minutes at a pace that they felt comfortable.

Read the detailed description

The current protocol has been used by Boolani, et al, 2017 to induce cognitive fatigue in college age individuals between the ages of 18-45 to test the effectiveness of cocoa and caffeinated cocoa in attenuating fatigue. It is our goal to explore the effects of standing desks as well as intermittent walking during cognitively fatiguing tasks and determine whether their use can attenuate mental fatigue in individuals between the ages of 18-45 years while performing cognitively challenging tasks.

02

Conditions studied

  • Sitting Position
  • Overexertion From Maintaining Prolonged Standing Position
  • Walking
03

In context

Lead sponsor

Clarkson University is the lead sponsor of 7 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 45 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • 18-45 years in age

Exclusion criteria

Exclusion Criteria:

  • Use of any prescription medications for any chronic conditions
  • current acute illness
  • chronic illnesses
  • color blindness
  • inability to stand for 90 minutes
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Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Single (Outcomes assessor)
Enrollment
31 participants (actual)

Study arms

  • Active comparator
    Sitting desk

    Participants were asked to perform all tasks in a sitting condition

    Behavioral: Performance of cognitive tasks

  • Experimental
    Standing desk

    Participants were asked to perform all tasks while standing

    Behavioral: Performance of cognitive tasks

  • Experimental
    Intermittent walking

    Participants were asked to walk for 2 minutes at a self-selected pace after 28 minutes of performing tasks while seated.

    Behavioral: Performance of cognitive tasks

Interventions

  • BehavioralPerformance of cognitive tasks

    Participants performed a series of cognitive tasks on all 3 days

06

What researchers measure

Primary outcomes

  1. Profile of Mood Survey- Short Form Vigor on a 0 to 20 scale from baseline to the end of the study

    Using the self-reported Profile of Mood Survey-Short Form participants reported their moods on the vigor scale of the POMS-SF

    Time frame: 28 minutes, 58 minutes, 88 minutes

  2. Profile of Mood Survey- Short Form Fatigue on a 0 to 20 scale from baseline to the end of the study

    Using the self-reported Profile of Mood Survey-Short Form participants reported their moods on the fatigue scale of the POMS-SF

    Time frame: 28 minutes, 58 minutes, 88 minutes

  3. Profile of Mood Survey- Short Form Tension on a 0 to 20 scale from baseline to the end of the study

    Using the self-reported Profile of Mood Survey-Short Form participants reported their moods on the tension scale of the POMS-SF

    Time frame: 28 minutes, 58 minutes, 88 minutes

  4. Profile of Mood Survey- Short Form Depression on a 0 to 20 scale from baseline to the end of the study

    Using the self-reported Profile of Mood Survey-Short Form participants reported their moods on the depression scale of the POMS-SF

    Time frame: 28 minutes, 58 minutes, 88 minutes

  5. Profile of Mood Survey- Short Form Anger on a 0 to 20 scale from baseline to the end of the study

    Using the self-reported Profile of Mood Survey-Short Form participants reported their moods on the anger scale of the POMS-SF

    Time frame: 28 minutes, 58 minutes, 88 minutes

  6. Changes on the Profile of Mood Survey- Short Form Confusion on a -4 to 16 scale from baseline to the end of the study

    Using the self-reported Profile of Mood Survey-Short Form participants reported their moods on the confusion scale of the POMS-SF

    Time frame: 28 minutes, 58 minutes, 88 minutes

  7. Changes in state mental energy were measured on a 0 to 300 scale from baseline to the end of the study

    Using the state mental and physical energy and fatigue scale participants reported their state mental energy.

    Time frame: 28 minutes, 58 minutes, 88 minutes

  8. Changes in state mental fatigue were measured on a 0 to 300 scale from baseline to the end of the study

    Using the state mental and physical energy and fatigue scale participants reported their state mental fatigue.

    Time frame: 28 minutes, 58 minutes, 88 minutes

  9. Changes in state physical fatigue were measured on a 0 to 300 scale from baseline to the end of the study

    Using the state mental and physical energy and fatigue scale participants reported their state physical fatigue.

    Time frame: 28 minutes, 58 minutes, 88 minutes

  10. Changes in state physical energy were measured on a 0 to 300 scale from baseline to the end of the study

    Using the state mental and physical energy and fatigue scale participants reported their state physical energy.

    Time frame: 28 minutes, 58 minutes, 88 minutes

Secondary outcomes

  1. Performance on the concentration task grid

    A 100 square grid was used as a measure of concentration. The grid is arranged in a 10x10 square with each square containing a two-digit number (from 00 to 99) which are randomly placed in the center of each of the squares. Participants were asked to mark off as many consecutive numbers as possible starting from 00 within a one-minute pe-riod, by tapping on the desired square

    Time frame: 15 minutes, 45 minutes, 75 minutes

  2. Performance on the continuous performance task

    Participants monitored a continuous series of letters (A-Z; Tahoma Regular font, size 20 point) presented on the screen for 1000ms and were asked to respond to the detection of the letter "X" only when preceded by the letter "A" by tapping on the screen or press-ing the "Space" key.

    Time frame: 6 minute, 36 minutes, 66 minutes

  3. Performance on the distractor task

    Identify the correct responses on the distractor tasks

    Time frame: 16 minutes, 46 minutes, 76 minutes

  4. Performance on the Erikson Flanker task

    During this task participants were first presented with a white fixation cross for 200ms, followed immediately by five equally sized arrows arranged in a 10.5cm horizontal ar-ray for 800ms. Participants were instructed to attend to the central arrow and ignore the four flankers. Participants were asked to press the left key if the central arrow was fac-ing left and the right arrow if the central arrow was pointed to the right. If all arrows were pointing the same direction (e.g. "\< \< \< \< \<") then the trial was considered con-gruent. However, if the central arrow was pointing the opposite direction (e.g. "\> \> \< \> \>") then the trial was considered incongruent. Subjects were presented with a 30 con-gruent and 30 incongruent trials in random order.

    Time frame: 19 minutes, 49 minutes, 79 minutes

  5. Performance on the Paced Visual Serial Addition Task

    Participants were asked to start at the number 0 and add the digit shown on the screen (0-9). Participants were then asked to remember the previous number and add the next digit presented on the screen and type their responses on the keypad.

    Time frame: 17 minutes, 47 minutes, 77 minutes

  6. Performance on the serial subtraction three task

    Participants were asked to silently subtract backwards in threes from a ran-dom number starting between 800 and 999 that was presented on the iPad screen

    Time frame: 2 minutes, 32 minutes, 62 minutes

  7. Performance on the serial subtraction seven task

    Participants were asked to silently subtract backwards in sevens from a ran-dom number starting between 800 and 999 that was presented on the iPad screen

    Time frame: 4 minutes, 34 minutes, 64 minutes

  8. Performance on the Rapid Visual Input Processing Task

    Participants were required to monitor a continuous series of digits (1-9; Tahoma Regu-lar font, size 20point) presented on the screen every 1000ms. The participants were given a primary, secondary, and tertiary task. The participant's primary task was to detect the presentation of three consecutive odd digits that were in ascending order (e.g. 3-7-9), the secondary task was to detect three consecutive even digits that were in ascending order (e.g. 2-4-8), and the tertiary task was to identify the number 6 when it was presented on the screen.

    Time frame: 14 minutes, 44 minutes, 74 minutes

  9. Performance on the Stroops task

    Participants were presented words (Tahoma font, 20point), every 1000ms on a screen spelling the names of colors (i.e. blue, yellow, red, green), which were either congru-ent (words presented in the same color as the color they were spelling out such as the RED presented in red font) or incongruent (words presented in a color different from the color that they spelled out such as the word RED spelled in green font). Participants were presented with all five options of colors used in this test (red, green, yellow, black, and blue) and asked to press the color of the text (font color) and not the word presented on the screen. There were 30 congruent and 30 incongruent tasks presented in random order and participants were scored on the number of correct responses, number of incorrect responses, and the average reaction time for correct responses. Each test was scored separately for both congruent and incongruent tasks

    Time frame: 18 minutes, 48 minutes, 78 minutes

  10. Performance on the Perceptual Fast Counting Task

    Participants were asked to press the number key that qualified with the number of dots presented on the screen. Each dot was approximately 0.5cm in diameter and the num-ber of dots on the screen ranged from 4 to 7. The number of dots was randomized across each trial and trials lasted 1 minute. Participants were scored based on number of correct responses, average reaction time for each correct response and the total num-ber of trials conducted in one minute

    Time frame: 20 minutes, 50 minutes, 80 minutes

07

Study locations

1 site
  • Clarkson University
    Potsdam, New York 13699, United States
08

References and documents

Individual participant data

Plan to share: No — Due to IRB restrictions no individual data will be shared with other researchers. All data will be reported as aggregate.

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 8, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07576413
Lead sponsor
Clarkson University
Responsible party
Sponsor
First posted
May 8, 2026
Start date
Jun 1, 2018
Primary completion
Dec 15, 2018
Completion
Dec 15, 2018
Last update
May 8, 2026

Study contacts

Ali Boolani, PhD
principal investigator · Clarkson University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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