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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02479477
Other study ID # 14076613.0.0000.5479
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 2015
Est. completion date September 2015

Study information

Verified date September 2020
Source Faculdade de Ciências Médicas da Santa Casa de São Paulo
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The quality of life and daily activities can be affected by muscleskeletal pain and one of the forms of assessment is through the SF-36 questionnaire. The investigators know that the working kinesitherapy is a way to improve the quality of life.


Description:

The activities in the work routine can cause pain and negatively affect quality of life. There is the hypothesis that gymnastics may be used for pain and injuries relating to repetitive movement at work. Objective the study is assess the impact of labor kinesiotherapy in the quality of life of the operating room nursing assistants.


Recruitment information / eligibility

Status Completed
Enrollment 46
Est. completion date September 2015
Est. primary completion date August 2015
Accepts healthy volunteers No
Gender All
Age group 18 Years to 55 Years
Eligibility Inclusion Criteria:

- professional nursing assistants allocated in the surgical center at least one year

- both genders

- who agreed to participate in the study by signing the informed consent

Exclusion Criteria:

- persons submitted on any surgery in the last six months

- with illness or muscle-skeletal disabilities

- or who couldn't attend all sessions for vacations or scale

Study Design


Related Conditions & MeSH terms


Intervention

Other:
kinesio therapy
during for fifteen minutes the nursing assistants will perform stretching exercises and muscle relaxation of large muscle groups the orthostatic position

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Faculdade de Ciências Médicas da Santa Casa de São Paulo

Outcome

Type Measure Description Time frame Safety issue
Primary change in questionnaire score after the intervention (minimum 0, maximum 100) SF-36 domains two months
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