Effectiveness of a Distance Eduaction Course for Prevention in RSI/WRMD
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT03385954|
Recruitment Status : Recruiting
First Posted : December 29, 2017
Last Update Posted : January 3, 2018
|Condition or disease||Intervention/treatment||Phase|
|Work-related Injury||Other: Intervention Other: Control||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||76 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Official Title:||Effectiveness of a Distance Eduaction Course for Prevention in RSI/WRMD on Life Quality of a Nursing Group|
|Actual Study Start Date :||March 1, 2017|
|Estimated Primary Completion Date :||March 30, 2019|
|Estimated Study Completion Date :||March 30, 2019|
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.
Wiil receive a lecture of 30 minutes
will receive a lecture of 30 minutes.
- 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.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03385954
|Contact: Renata C Rocha da Silva, MDemail@example.com|
|Hospital de Clínicas de Porto Alegre||Recruiting|
|Pôrto Alegre, Rio Grande Do Sul, Brazil, 90035-903|
|Contact: Renata c Rocha da Silva, MD 555133598439 firstname.lastname@example.org|
|Contact: Rosane M Nery, PhD 555133598439 email@example.com|
|Principal Investigator: Antonio c dos Santos, PhD|
|Principal Investigator:||Antônio C dos Santos, PhD||Hospital de Clínicas de Porto Alegre|