Effect of Dynamic Sitting on Pain Development - Part 2
DynSit-Pain 2
1 other identifier
interventional
20
1 country
1
Brief Summary
As a follow-up project to the Dyn-Sit-Pain study, this research aims to investigate the overall health as well as the physical and mental well-being through dynamic office chairs. The development of an innovative dynamic office chair concept will be professionally and scientifically supported, and the developed prototypes will be examined within the framework of usability studies.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started May 2025
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 12, 2025
CompletedFirst Submitted
Initial submission to the registry
September 26, 2025
CompletedFirst Posted
Study publicly available on registry
September 29, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
March 31, 2027
September 29, 2025
September 1, 2025
1.6 years
September 26, 2025
September 26, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Mean change in subjective lower back pain (before vs. after work, weekly average) estimated by visual analogue scale (VAS)
Participants will rate their subjectively perceived lower back pain before and after a conventional occupational day on 5 consecutive days starting at baseline (week 1) and ending with the post-intervention visit (week 6). Subjectively perceived lower back pain will be assessed with a Visual Analogue Scale (VAS). The VAS used for this study ranges from 0 (none) to 100 points (strongest pain imaginable). Question: Please rate the level of your lower back pain at this moment.
6 weeks
Secondary Outcomes (6)
Mean change in subjective mental fatigue (before vs. after work, weekly average) estimated by VAS
6 weeks
Mean subjectively rated work performance (after work, weekly average) estimated by VAS
6 weeks
Change in impact of pain on the daily life (pre vs. post intervention) estimated by ODI-D
6 weeks
Usability estimated using the UEQS questionnaire
6 weeks
Sitting behaviors estimated by microcontrollers
6 weeks
- +1 more secondary outcomes
Study Arms (4)
Study Track 1: Group A
EXPERIMENTALThe pre-existing static office chair will be used in the personal workplace for the first 6 weeks within the first half of the study. A wash-out period of a minimum of 4 weeks will be executed after the first half of the study. A dynamic office chair (saddle chair with standard pendulum mechanism) will be used on the personal workstation for 6 weeks within the second half of the study after the wash-out period.
Study Track 1: Group B
EXPERIMENTALA dynamic office chair (saddle chair with standard pendulum mechanism) will be used in the personal workplace for the first 6 weeks within the first half of the study. A wash-out period of a minimum of 4 weeks will be executed after the first half of the study. The pre-existing static office chair will be used on the personal workstation for 6 weeks within the second half of the study after the wash-out period.
Study Track 2: Group C
EXPERIMENTALThe pre-existing static office chair will be used in the personal workplace for the first 6 weeks within the first half of the study. A wash-out period of a minimum of 4 weeks will be executed after the first half of the study. A dynamic office chair (office swivel chair with integrated newly developed pendulum mechanism) will be used on the personal workstation for 6 weeks within the second half of the study after the wash-out period.
Study Track 2: Group D
EXPERIMENTALA dynamic office chair (office swivel chair with integrated newly developed pendulum mechanism) will be used in the personal workplace for the first 6 weeks within the first half of the study. A wash-out period of a minimum of 4 weeks will be executed after the first half of the study. The pre-existing static office chair will be used on the personal workstation for 6 weeks within the second half of the study after the wash-out period.
Interventions
The dynamic office chair has a typical office chair design (e.g. seat pan and a lumbar support). The seat pan is mounted on a flexible mechanic construction that allows hip movements in the frontal plane while sitting.
The dynamic office chair has a typical office chair design (e.g. seat pan and a lumbar support). The seat pan is mounted on a flexible mechanic construction that allows hip movements in the frontal plane while sitting.
Eligibility Criteria
You may qualify if:
- Signed Informed consent
- People aged between 18 and 65 years
- People classified as pain developers (e.g.: a 10 mm increase in pain on a 100 mm paper-based VAS)
- Office workers
- Employment status: \> 25 h / week
- Sufficient knowledge of German (min. B2 level)
- Body height of at least 160cm required
- Electrically or manually height-adjustable table at main workstation
You may not qualify if:
- Physical or mental limitations that make dynamic sitting or use of the procedure chair difficult (e.g. wheelchair users, vestibular dysfunction)
- Pregnancy
- Sitting for less than 20 hours per week at the main workplace
- Body weight over 110 kg and a body height over 195 cm
- Regular therapy or medication for pain or medication that affects the perception of pain (e.g. certain psychotropic drugs according to the package leaflet)
- office chair to which it is not possible to attach the swivel mechanism prototype
- Presence of any chronic disease that may influence pain perception (e.g., chronic kidney disease, fibromyalgia, neuropathy, chronic fatigue syndrome)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Applied Sciences for Health Professions Upper Austria
Linz, Upper Austria, 4020, Austria
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 26, 2025
First Posted
September 29, 2025
Study Start
May 12, 2025
Primary Completion (Estimated)
December 31, 2026
Study Completion (Estimated)
March 31, 2027
Last Updated
September 29, 2025
Record last verified: 2025-09
Data Sharing
- IPD Sharing
- Will not share