Impact of Labour Kinesiotherapy in the Quality Life of Auxiliary Nursing in the Surgery Center

September 4, 2020 updated by: Vera Lucia dos Santos Alves, Faculdade de Ciências Médicas da Santa Casa de São Paulo
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.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed 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.

Study Type

Interventional

Enrollment (Actual)

46

Phase

  • Not Applicable

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

18 years to 55 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

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 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: Crossover Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: kinesio therapy

The intervention is one protocol of labour kinesiotherapy that will be realized tree times per week, eatch intervention with fiveteen minutes, during eitgh weeks.

To change to sf-36 questionary after intervention. the intervention is the use of labour kinesio terapy in the auxiliary nursing The chance is in the score of questionary, the investigators hope that after intervention the score will increase.

during for fifteen minutes the nursing assistants will perform stretching exercises and muscle relaxation of large muscle groups the orthostatic position
No Intervention: control
the control group will continue their daily tasks uring eitgh weeks. To change to sf-36 questionary after intervention. the intervention is the use of labour kinesio terapy in the auxiliary nursing The chance is in the score of questionary, the investigators hope that after intervention the score will increase.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
change in questionnaire score after the intervention (minimum 0, maximum 100)
Time Frame: two months
SF-36 domains
two months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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

July 1, 2015

Primary Completion (Actual)

August 1, 2015

Study Completion (Actual)

September 1, 2015

Study Registration Dates

First Submitted

June 18, 2015

First Submitted That Met QC Criteria

June 21, 2015

First Posted (Estimate)

June 24, 2015

Study Record Updates

Last Update Posted (Actual)

September 9, 2020

Last Update Submitted That Met QC Criteria

September 4, 2020

Last Verified

September 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • 14076613.0.0000.5479

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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