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The Effect of a Structured Personalised Ergonomic Intervention for Hospital Nurses With Musculoskeletal Complains

Study That Examined the Effect of a Structured Personalised Ergonomic Intervention Program for Hospital Nurses With Musculoskeletal Complains.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01451567
Enrollment
31
Registered
2011-10-13
Start date
2005-06-30
Completion date
2006-03-31
Last updated
2011-10-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Musculoskeletal Diseases

Keywords

Nurses, Workload, Musculoskeletal System, Intervention

Brief summary

The purpose of this study is to examine the effect of a structured personalised ergonomic intervention program for hospital nurses with musculoskeletal complains.

Detailed description

In a randomised controlled trial 31 nurses with musculoskeletal complains were observed at work, and an intervention program was completed in 14 nurses with the other 17 acting as controls. The intervention included four meetings during three months. Outcome measures were collected before the intervention and post-tests were gathered three months after the determination of the program.

Interventions

BEHAVIORALErgonomic plan

participants in the intervention group were evaluated by the REBA and received an overall coaching that stretched over four meetings Each session paid special attention to, and included explanations about, the anatomy and physiology of body regions

Sponsors

Tel Aviv University
CollaboratorOTHER
Meir Medical Center
CollaboratorOTHER
Navah Ratzon
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
Yes

Inclusion criteria

* A minimum of half-time work for at least one year * musculoskeletal pain complaints * agreement to participate in the interventional study.

Exclusion criteria

* Male nurses * nurses with previously defined job restrictions and * pregnancy

Design outcomes

Primary

MeasureTime frame
Level of stress and control at work, measured by Karasek's questionnaire and Reba6 monthes

Secondary

MeasureTime frame
The prevalence and the level of pain measured by Nordic Questionnaire6 months

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026