Prevention and Intervention of Neck Pain in Swiss Office-Workers

NCT04169646 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2023-03-22

No results posted yet for this study

Summary

This study is the first that investigates the impact of a multi-component intervention combining current evidence of effective interventions with an adherence app to assess the potential benefits on productivity, neck pain, and headache.

Conditions

  • Neck Pain
  • Headache
  • Musculoskeletal Diseases
  • Adherence, Patient
  • Absenteeism
  • Workplace
  • Health Promotion
  • Ergonomics
  • Efficiency
  • Presenteeism
  • Occupational Health
  • Surveys and Questionnaires
  • Adult
  • Exercise Therapy
  • Work Performance

Interventions

OTHER

Multi-component intervention

Participants' workstation ergonomics will be assessed using an observation-based ergonomics assessment checklist for office-workers adapted to Swiss guidelines. Based on the initial assessment, best practice ergonomics will be applied individually using existing infrastructure. Participants will attend health promotion information group workshops for approximately one hour per week for 12 weeks. it. Participants will receive an individual progressive exercise programme aimed at conditioning the muscles of the neck and shoulder girdle. The exercises will be performed in groups (maximum of ten per group) at the workplace in a dedicated room, for approximately one hour (3x20 minutes) per week; once per week supervised by a physiotherapist, a human movement scientist, or a health scientist, and twice per week individually. Workshop session attendance will be recorded as an indication of adherence to health promotion. Adherence to neck exercises will be recorded with the Physitrack® app.

OTHER

Control

No intervention takes place during the control phase.

Sponsors & Collaborators

  • Swiss National Science Foundation

    collaborator OTHER
  • Zurich University of Applied Sciences

    lead OTHER

Principal Investigators

  • Markus Melloh, Prof · ZHAW School of Health Professions

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-10-28
Primary Completion
2022-07-31
Completion
2022-07-31

Countries

  • Switzerland

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04169646 on ClinicalTrials.gov