- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04610073
The Effect of Interactive Multimedia Versus Illustrated Booklet on Behavior to Prevent Lower Back Pain in Working Nurses.
October 29, 2020 updated by: Nahid Zarifsanaiey
Comparison of the Effect of Interactive Multimedia Versus Illustrated Booklet on Behavior to Prevent Lower Back Pain in Working Nurses in the Hospitals Affiliated to Shiraz University of Medical Sciences.
The present study was conducted to compare the effect of interactive multimedia and illustrated booklet methods on knowledge, attitude and improvement of behavior in preventing lower back pain amongst lower back pain amongst nurses.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
In this single blind randomized controlled trial, 153 eligible nurses working in hospitals during 2019 were enrolled.
The participants were randomly allocated into three parallel groups: interactive multimedia (n=55), illustrated booklet (n= 55), and the control (n= 43).
The study samples were blinded to intervention and control groups.
A researcher-made questionnaire was completed by the eligible subjects before, after, and four weeks after the intervention to assess their knowledge, attitude and behavior in preventing chronic lower back pain amongst working nurses.
Study Type
Interventional
Enrollment (Actual)
153
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
-
-
Fars
-
Shiraz, Fars, Iran, Islamic Republic of, 1846-71345
- Shiraz University of Medical Sciences
-
-
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
- CHILD
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Minimum education level of bachelor's degree in nursing
- Employment in governmental hospitals
- Willing to participate in the study and complete the informed consent
- Minimum knowledge of working with computers
Exclusion Criteria:
- Congenital anomalies
- low back pain
- History of back surgery
- History of trauma to the back
- Pregnancy
- Severe osteoporosis
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: HEALTH_SERVICES_RESEARCH
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: SINGLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: Interactive multimedia training
the intervention group 1 completed the pretest knowledge, attitude, and behavior questionnaire.
Then, interactive multimedia was made available to this group.
The questionnaire was completed again by the group, one week after completion of training, and then one month afterward.
|
The experimental groups conducted interactive multimedia training and illustrated booklet
|
|
EXPERIMENTAL: illustrated booklet
First, the intervention group 2 completed the pretest knowledge, attitude, and behavior questionnaire.
Then, illustrated booklet was made available to this group.
The questionnaire was completed again by the group one week after completion of training, and then one month afterward.
|
The experimental groups conducted interactive multimedia training and illustrated booklet
|
|
EXPERIMENTAL: No Intervention
In the control group, no intervention was performed.
Only before the intervention, one week and one month after the intervention, they completed the knowledge, attitude and behavior questionnaires.
|
The experimental groups conducted interactive multimedia training and illustrated booklet
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Behavior of the employed nurses in order to prevent low back pain
Time Frame: 5 weeks
|
Researcher made questionnaire for measuring behavior with 19 questions based on a six-point Likert scale.
|
5 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Knowledge of the employed nurses in order to prevent low back pain
Time Frame: 5 weeks
|
A Researcher made questionnaire for measuring knowledge with 10 four-option questions.
|
5 weeks
|
|
Attitude of the employed nurses in order to prevent low back pain
Time Frame: 5 weeks
|
A researcher made questionnaire for measuring attitude with 18 questions based on a six-point Likert scale.
|
5 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Nahid zarifsanaiey, PhD, associate Professor, Virtual school, Shiraz University of Medical Sciences, Shiraz, Iran.
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)
June 30, 2019
Primary Completion (ACTUAL)
July 28, 2019
Study Completion (ACTUAL)
December 29, 2019
Study Registration Dates
First Submitted
October 26, 2020
First Submitted That Met QC Criteria
October 26, 2020
First Posted (ACTUAL)
October 30, 2020
Study Record Updates
Last Update Posted (ACTUAL)
November 2, 2020
Last Update Submitted That Met QC Criteria
October 29, 2020
Last Verified
October 1, 2020
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IR.SUMS.REC.1397.1093
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
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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