The Effect of a Structured Personalised Ergonomic Interve... | NCT01451567

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

NCT01451567

Sponsor

Navah Ratzon

Status

Completed

Last Update Posted

Oct 18, 2011Estimated

Enrollment

31Actual

Phase

Not Applicable

Conditions

Musculoskeletal Diseases

Interventions

Ergonomic plan

Countries

Israel

Protocol Section

Identification Module Status Module Sponsor/Collaborators Module Oversight Module Description Module Conditions Module Design Module Arms/Interventions Module Outcomes Module Eligibility Module Contacts/Locations Module References Module IPD Sharing Statement Module

Results Section

Participant Flow Module Baseline Characteristics Module Outcome Measures Module Adverse Events Module More Info Module

Annotation Section

Annotation Module

Document Section

Large Document Module

Derived Section

Miscellaneous Info Module Condition Browse Module Intervention Browse Module

Protocol Section

Identification Module

NCT ID

Results Section

No data available

No data is available for this block.

Annotation Section

No data available

No data is available for this block.

Document Section

No data available

No data is available for this block.

Derived Section

Miscellaneous Info Module

Version Holder

Status Module

Record Verification Date

May 2005

Overall Recruitment Status or Expanded Access Status

Completed

Last Known Status

Not provided

Delayed Posting

Not provided

Why Stopped

Not provided

Expanded Access Info

Start Date

Jun 2005

Primary Completion Date

Oct 2005Actual

Completion Date

Mar 2006Actual

First Submitted Date

Oct 11, 2011

First Submission Date that Met QC Criteria

Oct 12, 2011

First Posted Date

Oct 13, 2011Estimated

Results Waived

Not provided

Results First Submitted Date

Not provided

Results First Submitted that Met QC Criteria

Not provided

Results First Posted Date

Not provided

Certification/Extension (aka Delayed Results) First Submitted Date

Not provided

Certification/Extension First Submitted that Passed QC Review

Not provided

Certification/Extension First Posted Date

Not provided

Last Update Submitted Date

Oct 15, 2011

Last Update Posted Date

Oct 18, 2011Estimated

Name	Class
Tel Aviv University	OTHER
Meir Medical Center	OTHER

Oversight Module

Has Data Monitoring Committee (DMC)

Yes

Is FDA Regulated Drug

Not provided

Is FDA Regulated Device

Not provided

Is Unapproved Device

Not provided

Pediatric Postmarket Surveillance of a Device Product

Not provided

Product Exported from US

Not provided

FDAAA801 Violation

Not provided

Description Module

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.

Design Module

Study Type

Interventional

Number of References to an Expanded Access Study

Not provided

Expanded Access Types

Not provided

Patient Registry

Not provided

Target Follow-Up Duration

Not provided

Phases

Not Applicable

Interventional Study Design

Allocation

Biospecimen

No data available

No data is available for this block.

Enrollment

31Actual

Arms/Interventions Module

Arm Groups

Not provided

Interventions

Name	Type	Description	Arm Group Labels	Other Names
Ergonomic plan	Behavioral	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		Ergonomic Intervintion Musculoskeletal System

Outcomes Module

Primary Outcomes

Measure	Description	Time Frame
Level of stress and control at work, measured by Karasek's questionnaire and Reba		6 monthes

Secondary Outcomes

Measure	Description	Time Frame
The prevalence and the level of pain measured by Nordic Questionnaire		6 months

Other Outcomes

Not provided

Eligibility Module

Eligibility Criteria

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

Accepts Healthy Volunteers

Yes

Sex

Female

Sex/Gender Based

Not provided

Sex/Gender Description

Not provided

Minimum Age

Not provided

Maximum Age

Not provided

Standard Ages

ChildAdultOlder Adult

Study Population

Not provided

Sampling Method

Not provided

Contacts/Locations Module

Central Contacts

Not provided

Overall Officials

Name	Affiliation	Role
Netta Abraham Bar-Niv, MA	Tel Aviv University	Principal Investigator

Locations

Facility	Status	City	State	ZIP	Country	Contacts
Tel Aviv University		Tel Aviv		69978	Israel

Condition Browse Module

MeSH Terms

ID	Term
D009140	Musculoskeletal Diseases

Ancestor Terms

Not provided

Browse Leaves

Not provided

Browse Branches

Not provided

Intervention Browse Module

MeSH Terms

ID	Term
D041641	Musculoskeletal Development

Ancestor Terms

ID	Term
D038081	Organogenesis
D005314	Embryonic and Fetal Development
D009024	Morphogenesis
D048788	Growth and Development

Browse Leaves

Not provided

Browse Branches

Not provided