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CompletedNCT06463041Updated Feb 24, 2026

How Does Implementing a GetUp Assist Device in Addition to a Daily Low-intensity Functional or Traditional Training Program Affect Norwegian Female Office Workers' Physical Health After 12 Weeks?

An interventional study of Experimental, comparator and control in Neck, Shoulder and Arm Syndrome, sponsored by Aalborg University. Completed at 1 site in Norway. Open to female participants aged 25 Years to 55 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-02-24.

Sponsored by Aalborg University · Not applicable, Interventional, and Other

Phase
Not applicable
Study type
Interventional
Enrollment
58
Allocation
Randomized
Ages
25 Years to 55 Years
Sex
Female
01

Study summary

This study aims to quantify the effect of daily transition routines between sitting and standing behaviour with an additional daily low-intensity traditional or functional training program on the physical health of sedentary Norwegian female workers after 12 weeks of implementation into their working environment.

02

Conditions studied

  • Neck, Shoulder and Arm Syndrome
03

In context

Lead sponsor

Aalborg University is the lead sponsor of 178 studies on the registry; 37 are open to participants now.

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

04

Who can participate

Ages eligible
25 Years to 55 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

Inclusion criteria

  • Females are included in this study due to the approximately twice-high prevalence of work-related musculoskeletal disorders.
  • No experience with office fit training or participation in an ongoing similar training intervention is allowed.
  • Working more than 6 hours a day at a computer workstation
  • Physical inactivity (less than two sessions or bouts of exercise totalling 30 minutes/week).
  • Musculoskeletal complaints are accepted as long as the pain is not a restricting factor. when performing the testing and training intervention exercises.

Exclusion criteria

Exclusion Criteria:

  • Participants not able to perform the testing battery.
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Factorial assignment
Masking
None (open label)
Enrollment
58 participants (actual)

Study arms

  • Experimental
    Functional training group

    Functional training group that will perform a short, low-intensity, 10-minute hole-body exercise program per day before the lunch break, in addition to following the getup assistance during the working day.

    Other: Experimental, comparator and control

  • Active comparator
    Traditional training group

    Traditional training group that will perform a short, low-intensity, 10-minute hole-body exercise program per day before the lunch break, in addition to following the getup assistance during the working day.

    Other: Experimental, comparator and control

  • No intervention
    Negative control

    Control group. A group that is not treated.

Interventions

  • OtherExperimental, comparator and control

    How does implementing a GetUp Assist device in addition to a daily low-intensity functional or traditional training program affect Norwegian female office workers' physical health after 12 weeks?

06

What researchers measure

Primary outcomes

  1. Norwegian Short-Form Health Survey (SF-36)

    Measure (i) physical function, (ii) Energy/fatigue, (iii) pain, and (iv) general health

    Time frame: 3 months

  2. Neck and shoulder trouble questionnaire from the Nordic musculoskeletal questionnaire

    Measure neck-shoulder discomfort

    Time frame: 3 months

  3. Numeric rating scale

    Measure neck-shoulder discomfort from 0-10 scale, with zero meaning "no pain" and 10 meaning "the worst pain imaginable

    Time frame: 3 months

  4. Y-balance test

    Quantify dynamic postural control

    Time frame: 3 months

  5. The Danish step test

    Estimating cardiorespiratory fitness

    Time frame: 3 months

  6. Chair-sit-and-reach test

    Measuring hamstrings flexibility

    Time frame: 3 months

  7. Back scratch test

    Measuring upper-body/ shoulder flexibility

    Time frame: 3 months

  8. CS-30 test

    Measuring lower-body strength

    Time frame: 3 months

  9. Hand Grip Strength test

    Measuring hand Grip Strength

    Time frame: 3 months

07

Study locations

1 site
  • SSA Steinkjer
    Steinkjer, Nord-Trøndelag 7711, Norway
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 24, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06463041
Lead sponsor
Aalborg University
Collaborators
The Research Council of Norway
Responsible party
Lasse Engberg Treu Lassen (Ph.D., Aalborg University) — Principal investigator
First posted
Jun 17, 2024
Start date
Sep 2, 2024
Primary completion
Dec 22, 2024
Completion
Dec 22, 2024
Last update
Feb 24, 2026

Oversight

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

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This study is completed, as verified in Feb 2026. You cannot join it, but the record below documents what was studied.

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