Effectiveness of a Distance Eduaction Course for Prevention in RSI/WRMD

Sponsor
Hospital de Clinicas de Porto Alegre (Other)
Overall Status
Unknown status
CT.gov ID
NCT03385954
Collaborator
(none)
76
1
2
24.9
3

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Intervention
  • Other: Control
N/A

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 Design

Study Type:
Interventional
Anticipated Enrollment :
76 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Effectiveness of a Distance Eduaction Course for Prevention in RSI/WRMD on Life Quality of a Nursing Group
Actual Study Start Date :
Mar 1, 2017
Anticipated Primary Completion Date :
Mar 30, 2019
Anticipated Study Completion Date :
Mar 30, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention

distance education curse with 8 hours to be accomplished in 2 weeks,

Other: Intervention
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

Other: Control
will receive a lecture of 30 minutes.

Outcome Measures

Primary Outcome Measures

  1. Quality of life [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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hospital de Clínicas de Porto Alegre Pôrto Alegre Rio Grande Do Sul Brazil 90035-903

Sponsors and Collaborators

  • Hospital de Clinicas de Porto Alegre

Investigators

  • Principal Investigator: Antônio C dos Santos, PhD, Hospital de Clínicas de Porto Alegre

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Hospital de Clinicas de Porto Alegre
ClinicalTrials.gov Identifier:
NCT03385954
Other Study ID Numbers:
  • 160415
First Posted:
Dec 29, 2017
Last Update Posted:
Jan 3, 2018
Last Verified:
Oct 1, 2017
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Hospital de Clinicas de Porto Alegre

Study Results

No Results Posted as of Jan 3, 2018