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Effect of Dynamic Sitting on Pain Development (DynSit-Pain)

U

University of Applied Sciences for Health Professions Upper Austria

Status

Completed

Conditions

Lower Back Pain

Treatments

Device: Dynamic office chair

Study type

Interventional

Funder types

Other

Identifiers

NCT05664776
DynSit-Pain

Details and patient eligibility

About

Worksite based prolonged static sitting postures can cause musculoskeletal pain. While the development of pain increases due to the constant growth of digitalization at work, numerous interventions to reduce prolonged sitting periods have been created. The effects of such interventions have not yet been properly examined. Thus, the "DynSit-Pain" project was initiated to investigate the influence of dynamic sitting on the pain development of pain developers in office environments.

Full description

This clinical investigation is a prospective, randomized, controlled, counter-balanced, two-arm field study investigating the effect of dynamic sitting on musculoskeletal pain in office workers classified as pain developers.

The study consists of a pre-screening visit and 4 assessment days / visits. During this pre-screening visit and after proving the study eligibility (inclusion / exclusion criteria), half of the study participants will randomly be allocated to one of the two study arms. Depending on the arm allocation, participants will receive a dynamic (= intervention) or static (= control) office chair for 6 weeks. After a wash-out of at least 4 weeks the 6-week intervention resp. control will be switched. The randomization will be realized with opaque envelopes.

Overall participants will execute the identical assessments within the control and the intervention chair group. The wash-out phase between the control and the intervention periods will ensue identical baseline conditions for both chairs. The overall duration of study participation amounts to 16 weeks.

Enrollment

13 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Signed informed consent
  • People aged between 18 and 65 years
  • People classified as pain developers (e.g., increase of pain of 10 mm on a 100 mm paper based visual analogue scale) determined by pre-screening
  • Office workers
  • Employment status: > 30 h / week
  • Sufficient German language skills (minimum B2 level)
  • Table height of at least 63 cm at the main workplace

Exclusion criteria

  • Physical or mental limitations that aggravate dynamic sitting or using the interventional chair (e.g., wheel chair users, vestibular dysfunctions)
  • Pregnancy
  • Working in sitting posture for less than 20 hours per working week in the main workplace.
  • Bodyweight over 110 kg and a body height over 195 cm
  • Regular therapy or medication for pain

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

13 participants in 2 patient groups

Arm A (control first)
Experimental group
Description:
The 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 will be used on the personal workstation for 6 weeks within the second half of the study after the wash-out period.
Treatment:
Device: Dynamic office chair
Arm B (intervention first)
Experimental group
Description:
A dynamic 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. 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.
Treatment:
Device: Dynamic office chair

Trial contacts and locations

1

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Central trial contact

Bernhard Schwartz, Dr. BSc MSc

Data sourced from clinicaltrials.gov

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