Effect of Dynamic Sitting on Pain Development - Part 2
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Dynamic office chair (saddle chair with standard pendulum mechanism), Dynamic Office Chair (office swivel chair with integrated newly developed pendulum mechanism).
- Who it may be relevant to
- Registry conditions: Lower Back Pain. Basic parameters: 18 years — 65 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Austria
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Effect of Dynamic Sitting on Pain Development - Part 2 - a Randomized Controlled Cross-over Study
Overview
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.
Detailed description
This clinical trial is a prospective, randomised, controlled, open-label study with two tracks, each in a cross-over design investigating the effect of of two dynamic office chairs (saddle chair with standard pendulum mechanism \[Smart Moving Technology\], study track 2 = office swivel chair with integrated newly developed pendulum mechanism \[Smart Moving Technology New\]) on the musculoskeletal system of office workers classified as pain developers.
The study consists of a pre-screening visit and 4 assessment days / visits. After proving eligibility for the study (inclusion/exclusion criteria), subjects are assigned to one of the two study tracks. Subjects are randomised to one of the two study tracks and then to the respective group (Group A to D).
* Study track 1: saddle chair with standard pendulum mechanism (= intervention 1) + static office chair (= control) * Study track 2: office swivel chair with integrated newly developed pendulum mechanism (= intervention 2) + static office chair (= control).
Depending on the study track and group allocation, the test subjects first receive a dynamic office chair (= intervention) or a static office chair (= control). The randomization will be realized with opaque envelopes in different colours and follows international recommendations.
Overall participants will execute identical assessments. A wash-put period between the control and the intervention phases ensures identical baseline conditions. The overall duration of study participation equals 16 weeks.
Interventions
- Device Dynamic office chair (saddle chair with standard pendulum mechanism)
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. - Device Dynamic Office Chair (office swivel chair with integrated newly developed pendulum mechanism)
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.
Primary outcome measures
- Mean change in subjective lower back pain (before vs. after work, weekly average) estimated by visual analogue scale (VAS) [Time frame: 6 weeks]
Secondary outcome measures (6)
- Mean change in subjective mental fatigue (before vs. after work, weekly average) estimated by VAS [Time frame: 6 weeks]
- Mean subjectively rated work performance (after work, weekly average) estimated by VAS [Time frame: 6 weeks]
- Change in impact of pain on the daily life (pre vs. post intervention) estimated by ODI-D [Time frame: 6 weeks]
- Usability estimated using the UEQS questionnaire [Time frame: 6 weeks]
- Sitting behaviors estimated by microcontrollers [Time frame: 6 weeks]
- Number of adverse events estimated from an AEs form sheet [Time frame: 16 weeks]
Eligibility criteria
Inclusion criteria
- 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
Exclusion criteria
- 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)
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Crossover
- Masking
- Open label
- Primary purpose
- Prevention
Study locations
Austria · 1 center
- University of Applied Sciences for Health Professions Upper Austria — Linz
Identifiers
NCT: NCT07197879 · 2025-05-12