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CompletedNCT00801983Updated Aug 22, 2014Results posted

The Effect of Alternative Keyboards on Discomfort and Typing Kinematics

An interventional study of Alternative Keyboard in Pain, sponsored by University of Pittsburgh. Completed at 1 site in United States. Open to participants aged 18 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2014-08-22.

Sponsored by University of Pittsburgh · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
85
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

Awkward postures during computer keyboard use have been hypothesized to be one cause of musculoskeletal pain/discomfort as well as musculoskeletal disorders of the upper extremity (MSD-UE). Alternative computer keyboards purport to reduce musculoskeletal pain/discomfort and have been shown to change aspects of keyboard users' kinematics under laboratory conditions. However, research that has examined the effectiveness of alternative keyboards in reducing musculoskeletal pain/discomfort in the workplace is equivocal, and no study has examined the association between postures and musculoskeletal pain. The Aims of this 3-year prospective double cross-over trial are: 1) To examine the effectiveness of an alternative keyboard in reducing reports of pain over 6-months; 2) To examine the neutrality and stability of postures during keyboard use; and 3) To identify which postures are associated with lower levels of musculoskeletal pain. Seventy-five computer users will be randomly assigned to one of two keyboard use orders: Group 1 - AB (standard keyboard, alternative keyboard); Group 2 - BA (alternative keyboard, standard keyboard). All subjects will use their assigned keyboards for 6-months before switching to the next keyboard. Every week, subjects will report their musculoskeletal pain levels. Just prior to and just after each 6-month intervention subjects' kinematics performances on the keyboards will be recorded at the worksite using the Keyboard - Personal Computing Style (K-PeCS) instrument and in a laboratory setting using 3-dimensional motion capture technology.

Aim 1: To examine the effectiveness of an alternative keyboard in reducing pain over 6-months.

Hypothesis 1 (H-1) - At six months subjects using an alternative keyboard will have significantly lower musculoskeletal pain levels than when using a standard keyboard.

Aim 2: To examine the neutrality and stability of postures during keyboard use.

Hypothesis 3 (H-2) - Subjects using an alternative keyboard will have significantly more neutral postures than when using a standard keyboard at baseline and at 6 months Hypothesis 3 (H-3) - Subjects 6-months keyboarding postures will remain equivalent to the keyboarding postures documented at baseline.

02

Conditions studied

  • Pain

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03

In context

Pain

2,450 studies on the registry are indexed under Pain; 945 are open to participants now.

This study's enrollment of 85 is above the median of 70 across 2,101 interventional studies indexed under Pain.

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Lead sponsor

University of Pittsburgh is the lead sponsor of 1,414 studies on the registry; 168 are open to participants now.

Of its 8 completed or terminated interventional studies of FDA-regulated products, 4 (50%) have results posted.

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

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Use a computer at least 20 hrs per week
  • Aged 18-65
  • Experiencing some pain during computer use

Exclusion criteria

Exclusion Criteria:

  • Currently use an alternative keyboard
  • Serious trauma injury to the upper extremity
  • Rheumatic disorder
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
85 participants (actual)

Study arms

  • Experimental
    A

    Subject receives typical keyboard first for 6 months and alternative keyboard second for 6 months

    Device: Alternative Keyboard

  • Experimental
    B

    Subject receives alternative keyboard first for 6 months and typical keyboard second for 6 months

    Device: Alternative Keyboard

Interventions

  • DeviceAlternative Keyboard

    Subjects use either a typical or alternative keyboard

    Also known as: Microsoft Natural Ergonomic

06

What researchers measure

Primary outcomes

  1. Musculoskeletal Discomfort

    Discomfort Survey (WDS) was used to assess symptoms and activity limitations. Participants reported on their work schedule, medication used for pain control, and discomfort in their neck/shoulder, back, and bilateral lower arms (elbows, forearms, wrists, and hands) using an 11-point numerical rating scale (0 = no discomfort/no limitations; 10 = unbearable discomfort/major limitations). We had to dichotomize the data during analysis due to severe skew towards not discomfort (0). Thus the final outcome was discomfort -yes or no

    Time frame: 6 months and 12 months

07

Results

Posted Aug 22, 2014

Participant flow

Period 1
Participant flow — Period 1
MilestoneGroup A (Typical/Alternative)Group B (Alternative/Typical)
Started4441
Completed4033
Not completed48
Withdrew: Lost to follow-up20
Withdrew: Withdrawal by subject28
Period 2
Participant flow — Period 2
MilestoneGroup A (Typical/Alternative)Group B (Alternative/Typical)
Started4033
Completed3832
Not completed21
Withdrew: Withdrawal by subject21

Outcome measures

PrimaryMusculoskeletal Discomfort

Discomfort Survey (WDS) was used to assess symptoms and activity limitations. Participants reported on their work schedule, medication used for pain control, and discomfort in their neck/shoulder, back, and bilateral lower arms (elbows, forearms, wrists, and hands) using an 11-point numerical rating scale (0 = no discomfort/no limitations; 10 = unbearable discomfort/major limitations). We had to dichotomize the data during analysis due to severe skew towards not discomfort (0). Thus the final outcome was discomfort -yes or no

Time frame:
6 months and 12 months
Reported as:
Number · percentage of subjects with MSD
Musculoskeletal Discomfort
percentage of subjects with MSDTypical KeyboardAlternative Keyboard
Musculoskeletal Discomfort2020
Statistical analysis
  • Typical Keyboard vs Alternative Keyboard · GEE · p = >.05

Adverse events

Non-serious events are listed at a 0% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Typical Keyboard—0/85 (0%)0/85 (0%)
Alternative Keyboard—0/85 (0%)0/85 (0%)

Baseline characteristics

GEE analyses allows a subjects inclusion even if they did not complete the full trial. Although we had a total of 15 subjects not complete the full trial we had sufficient data on 77 subjects to complete the GEE statistical analyses. With the crossover design we compared 77 subjects using the standard keyboard to 77 subjects using the alternative

Age, Continuous
Age, Continuous(years)Group AGroup BTotal
Mean43.3 ± 12.945.6 ± 11.944.4 ± 12.4
Sex: Female, Male
Sex: Female, Male(Participants)Group AGroup BTotal
Female363571
Male426
Race (NIH/OMB)
Race (NIH/OMB)(Participants)Group AGroup BTotal
American Indian or Alaska Native000
Asian101
Native Hawaiian or Other Pacific Islander000
Black or African American358
White363167
More than one race011
Unknown or Not Reported000
Ethnicity (NIH/OMB)
Ethnicity (NIH/OMB)(Participants)Group AGroup BTotal
Hispanic or Latino101
Not Hispanic or Latino393776
Unknown or Not Reported000
Region of Enrollment
Region of Enrollment(participants)Group AGroup BTotal
United States403777
Avg Computer Use
Avg Computer Use(hrs/day)Group AGroup BTotal
Mean6.3 ± 1.16.1 ± 1.56.2 ± 1.3
Typing Speed
Typing Speed(participants)Group AGroup BTotal
Slow7310
Moderately Fast161430
Fast111223
Don't know6814
Baseline Discomfort
Baseline Discomfort(participants)Group AGroup BTotal
Neck (Yes)363672
Back (Yes)333366
Right arm hand (Yes)333669
Left Arm hand (Yes)222446
08

Study locations

1 site
  • University of Pittsburgh
    Pittsburgh, Pennsylvania 15260, United States
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 22, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00801983
Collaborators
National Institute for Occupational Safety and Health (NIOSH/CDC)
Responsible party
Nancy Baker (Associate Professor, University of Pittsburgh) — Principal investigator
First posted
Dec 4, 2008
Start date
Jan 2009
Primary completion
Apr 2011
Completion
Aug 2013
Results posted
Aug 22, 2014
Last update
Aug 22, 2014

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Aug 2014. You cannot join it, but the record below documents what was studied.

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