- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05834959
Implementation of a Fitness Education and Training Program to Support Safe Patient Handling and Safe Lifting
November 14, 2023 updated by: Shelley Sargent, University of Manitoba
Implementation of a Fitness Education and Training Program to Support Safe Patient Handling and Safe Lifting in a Community Based Hospital (The Fit for Work Project)
This project involves the delivery of education and training sessions to Seven Oaks General Hospital (SOGH) staff, with the goal of workplace injury prevention.
Education will include review of provincial safe patient handling and back injury prevention guidelines and review of core fitness competencies required to comply with injury prevention standards.
Training sessions will include exercises to improve core, gluteal and quadricep strength, hip/knee mobility and hamstring flexibility.
Training will also be an opportunity to provide feedback on functional movement performance.
Outcomes will include questionnaires on: low back pain/dysfunction; movement confidence; work injury rates and participant satisfaction with program.
The project will advise stakeholders of the benefits and challenges associated with implementation of a fitness program to support safe patient handling techniques, as outlined in the provincial guidelines for healthcare workers.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The Fit for Work Project is an educational and training program outcome evaluation.
It is a two-part education and practical program designed to evaluate the effects of training on movement confidence, low back dysfunction and changes in rates of lower back injury.
In the first part, participants will attend the education session developed by physiotherapists who specialize in return to work programs.
In the second part participants will participate in a 4-week practical program, where they will stretch, lengthen and strengthen key muscles used in squatting, weight shifting and the hip hinge movement.
Feedback and movement coaching are an important element in performing and mastering these movements correctly and this workplace wellness training program will provide staff the support needed.
Study Type
Interventional
Enrollment (Actual)
55
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Manitoba
-
Winnipeg, Manitoba, Canada, R2P 2W7.
- The Wellness Institute
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Male or female, age 18 years or older
- Staff of Seven Oaks General Hospital during the time of the program
- Able to communicate in English and provide written informed consent
Exclusion Criteria:
- An acute injury, a medical condition, or other personal reason inhibiting participation in all 4 weeks of exercise training sessions
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: SOGH employees, taking part in the same education and training program.
Participants will be recruited from the Seven Oak General Hospital staff population and will complete a two-part education and practical program.
|
Education and practical training program designed to evaluate the effects of training on movement confidence, low back dysfunction and changes in rates of lower back injury
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from baseline in staff confidence in performing the core fitness competencies required to abide by safe patient handling, safe lifting and back injury prevention guidelines
Time Frame: At the beginning of the program (baseline), at week 4 (the end of the 4-week training program), and one year after completion of the training program
|
A Movement Confidence Questionnaire will be used, asking participants to rate their confidence as either 1-Very Low, 2-Low, 3-Moderate, 4-High, 5-Very High in completing 10 different movements without difficulty:
|
At the beginning of the program (baseline), at week 4 (the end of the 4-week training program), and one year after completion of the training program
|
|
Change from baseline in severity of low back pain and/or dysfunction
Time Frame: At the beginning of the program (baseline), at week 4 (the end of the 4-week training program), and one year after completion of the training program
|
Measured as change from baseline in the Quebec Back Pain Disability Scale (Designed to evaluate functional limitations related to pain, to monitor the progress of individual patients and to compare the evolution of lower back pain (LBP) subjects incorporated in rehabilitation programs)
|
At the beginning of the program (baseline), at week 4 (the end of the 4-week training program), and one year after completion of the training program
|
|
Change from baseline in severity of low back pain and/or dysfunction
Time Frame: At the beginning of the program (baseline), at week 4 (the end of the 4-week training program), and one year after completion of the training program
|
Measured as change from baseline in the Oswestry Disability Index, also known as the Oswestry Low Back Pain Disability Questionnaire.
(A self-reported measurement tool that measures both pain and functional status.
It is used for evaluating disability caused by lower backache).
|
At the beginning of the program (baseline), at week 4 (the end of the 4-week training program), and one year after completion of the training program
|
|
Change from baseline in incidence of back injuries
Time Frame: At the beginning of the program (baseline), and 1 year after completion of the 4-week training program
|
Measured as change in the number of new low back injuries or flare-ups of existing back conditions sustained in the past year.
|
At the beginning of the program (baseline), and 1 year after completion of the 4-week training program
|
|
Change from baseline in frequency of back injuries
Time Frame: At the beginning of the program (baseline), and 1 year after completion of the 4-week training program
|
Measured as the number of new low back injuries or flare-ups of existing back conditions sustained at work in the past year.
|
At the beginning of the program (baseline), and 1 year after completion of the 4-week training program
|
|
Change from baseline in time loss cost of back injuries
Time Frame: At the beginning of the program (baseline), and 1 year after completion of the 4-week training program
|
Measured as the duration of time away from work due to low back pain/injury.
|
At the beginning of the program (baseline), and 1 year after completion of the 4-week training program
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Benefits and challenges associated with implementation of a fitness program to support safe patient handling and safe lifting techniques, as outlined in the provincial and regional guidelines for healthcare workers
Time Frame: Collected at week 4 (at the end of the 4-week training program)
|
A "Program Exit Questionnaire" will be administered to collect participant experiences and views on the benefits and challenges associated with the program.
|
Collected at week 4 (at the end of the 4-week training program)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Shelley Sargent, BMRPT MSc, The Wellness Institute at Seven Oaks General Hospital
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 14, 2023
Primary Completion (Actual)
September 11, 2023
Study Completion (Actual)
October 30, 2023
Study Registration Dates
First Submitted
March 13, 2023
First Submitted That Met QC Criteria
April 17, 2023
First Posted (Actual)
April 28, 2023
Study Record Updates
Last Update Posted (Estimated)
November 17, 2023
Last Update Submitted That Met QC Criteria
November 14, 2023
Last Verified
November 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- HS25745 (H2022:355)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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