NCT06463041

Brief 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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
58

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Sep 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

June 8, 2024

Completed
9 days until next milestone

First Posted

Study publicly available on registry

June 17, 2024

Completed
3 months until next milestone

Study Start

First participant enrolled

September 2, 2024

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 22, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 22, 2024

Completed
Last Updated

February 24, 2026

Status Verified

February 1, 2026

Enrollment Period

4 months

First QC Date

June 8, 2024

Last Update Submit

February 22, 2026

Conditions

Outcome Measures

Primary Outcomes (9)

  • Norwegian Short-Form Health Survey (SF-36)

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

    3 months

  • Neck and shoulder trouble questionnaire from the Nordic musculoskeletal questionnaire

    Measure neck-shoulder discomfort

    3 months

  • Numeric rating scale

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

    3 months

  • Y-balance test

    Quantify dynamic postural control

    3 months

  • The Danish step test

    Estimating cardiorespiratory fitness

    3 months

  • Chair-sit-and-reach test

    Measuring hamstrings flexibility

    3 months

  • Back scratch test

    Measuring upper-body/ shoulder flexibility

    3 months

  • CS-30 test

    Measuring lower-body strength

    3 months

  • Hand Grip Strength test

    Measuring hand Grip Strength

    3 months

Study Arms (3)

Functional training group

EXPERIMENTAL

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

Traditional training group

ACTIVE COMPARATOR

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

Negative control

NO INTERVENTION

Control group. A group that is not treated.

Interventions

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?

Functional training groupTraditional training group

Eligibility Criteria

Age25 Years - 55 Years
Sexfemale(Gender-based eligibility)
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • 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.

You may not qualify if:

  • Participants not able to perform the testing battery.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

SSA Steinkjer

Steinkjer, Nord-Trøndelag, 7711, Norway

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
FACTORIAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Ph.D.

Study Record Dates

First Submitted

June 8, 2024

First Posted

June 17, 2024

Study Start

September 2, 2024

Primary Completion

December 22, 2024

Study Completion

December 22, 2024

Last Updated

February 24, 2026

Record last verified: 2026-02

Locations