- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03385954
Effectiveness of a Distance Eduaction Course for Prevention in RSI/WRMD
January 2, 2018 updated by: Hospital de Clinicas de Porto Alegre
Effectiveness of a Distance Eduaction Course for Prevention in RSI/WRMD on Life Quality of a Nursing Group
Repetitive Strain Injuries (RSI) or Work-Related Ostomuscular Disorders (WRMD) are musculoskeletal disorders.
Nursing is one of the categories of workers most affected, due to the inherent functions they perform in their daily activities.
The objective of this study is to evaluate the effects of a distance education program of prevention in RIS/WRMD on the quality of life of a nursing group.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed Description
Repetitive Strain Injury (RSI) or Work-Related Musculoskeletaldisorders (WRMD) are the names given to skeletal muscle disorders that mainly affect the upper limbs, the scapular region and the neck.
One of the most affected categories is nursing workers who present health problems inherent to the function they perform in their daily activities.
Due to this peculiarity, several studies are focused on the occupational risks of nursing workers in the hospital environment.
However, It was not found in the literature studies that suggests strategies to prevent and improve the worker's quality of life.
Distance education comes as a differential.
It has power in interactive media and collaborative learning beyond self-learning and mass media.
This research project proposes to carry out a randomized clinical trial where the intervention group will receive a Prevention Course in RSI/WRMD in the distance education modality and the control group will receive Educational Lectures on Prevention in RSI /WRMD, both groups will be composed by a nursing team from the Clinical Hospital of Porto Alegre.
Study Type
Interventional
Enrollment (Anticipated)
76
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
-
-
Rio Grande Do Sul
-
Pôrto Alegre, Rio Grande Do Sul, Brazil, 90035-903
- Recruiting
- Hospital de Clinicas de Porto Alegre
-
Contact:
- Renata c Rocha da Silva, MD
- Phone Number: 555133598439
- Email: renatatoufpel@gmail.com
-
Contact:
- Rosane M Nery, PhD
- Phone Number: 555133598439
- Email: rosane.nery@gmail.com
-
Principal Investigator:
- Antonio c dos Santos, PhD
-
-
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Nurse staff from HCPA
- Male and Female
- Individuals that agree to participate of the distance eduacational course
- Individuals that agree to participate in the research by signing the Term of Free and Clarified Consent
Exclusion Criteria:
- Individuals that do not complete the course
- Individuals that do not agree to participate in the research by signing the Term of Free and Clarified Consent
- Individuals with chronic musculoskeletal injury diagnosed.
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: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention
distance education curse with 8 hours to be accomplished in 2 weeks,
|
The distance eduacation group course has a workload of 8 hours and will be developed over 2 weeks.
It is suggested that students have a minimum of 1 hour of study per day.
The course will consist of work tips, clarifications and procedures for the prevention of RIS/WRMD physical training tips to improve cardiovascular condition and, of strength and flexibility, available literature and theoretical evidence that should be answered through the knowledge acquired in the EAD course of prevention of LERDORT from the HCPA's Physiatrics and Rehabilitation Service.
This Course will be available through moodle.
|
|
Experimental: Control
Wiil receive a lecture of 30 minutes
|
will receive a lecture of 30 minutes.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Quality of life
Time Frame: 48 months
|
Verified by instrument SF36 - With 36 items that measure eight domains (variables): functional capacity, physical aspects, pain, general health, vitality, social aspects, emotional aspects and mental health.
The highest score for each SF-36 domain is 100 and the lowest score is 0.
|
48 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Antônio C dos Santos, PhD, Hospital de Clinicas de Porto Alegre
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Corlett EN, Bishop RP. A technique for assessing postural discomfort. Ergonomics. 1976 Mar;19(2):175-82. doi: 10.1080/00140137608931530. No abstract available.
- Lincoln AE, Feuerstein M, Shaw WS, Miller VI. Impact of case manager training on worksite accommodations in workers' compensation claimants with upper extremity disorders. J Occup Environ Med. 2002 Mar;44(3):237-45. doi: 10.1097/00043764-200203000-00011.
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 1, 2017
Primary Completion (Anticipated)
March 30, 2019
Study Completion (Anticipated)
March 30, 2019
Study Registration Dates
First Submitted
December 21, 2017
First Submitted That Met QC Criteria
December 21, 2017
First Posted (Actual)
December 29, 2017
Study Record Updates
Last Update Posted (Actual)
January 3, 2018
Last Update Submitted That Met QC Criteria
January 2, 2018
Last Verified
October 1, 2017
More Information
Terms related to this study
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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