Investigation of Burnout, Musculoskeletal System and Aerobic Capacity in Nurses

November 15, 2024 updated by: Songül Bağlan Yentür, Firat University

Investigation of Burnout, Musculoskeletal System, Physical Performance and Perception of Exercise Benefit / Obstacle and Aerobic Capacity in Nurses

The aim of our study was to evaluate the relationship of aerobic capacity with burnout status, musculoskeletal system, physical performance and exercise benefit/obstacle perception in nurses, who have an important place in the health profession group, and to bring the results to the literature. Demographic information will be obtained from the participants who volunteered to participate in the study. Burnout, musculoskeletal pain and physical performance will be evaluated with relevant scales and aerobic capacity will be measured with a bicycle ergometer.

Study Overview

Status

Not yet recruiting

Conditions

Detailed Description

In the literature, there are studies on the general effects of aerobic exercises on the cardiovascular system, musculoskeletal system, endocrine system, nervous system and psychosocial status. However, despite the benefits of aerobic exercises and the physiological and psychological importance of high aerobic capacity, there are no studies in the literature that examine the factors associated with the aerobic capacity of nurses. These factors affect the professional life of nursesThe aim of our study was to evaluate the relationship of aerobic capacity with burnout status, musculoskeletal system, physical performance and exercise benefit/obstacle perception in nurses, who have an important place in the health profession group, and to bring the results to the literature. Demographic information will be obtained from the participants who volunteered to participate in the study. Burnout, musculoskeletal pain and physical performance will be evaluated with relevant scales and aerobic capacity will be measured with a bicycle ergometer.

Study Type

Observational

Enrollment (Estimated)

30

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Probability Sample

Study Population

The study will include 30 female nurses who work in Fırat University Hospital on normal shift and do not have any chronic disease.

Description

Inclusion Criteria:

  • 18-65 years old
  • At least 1 year of experience
  • Nurses not working in the academic field

Exclusion Criteria:

  • Pregnancy
  • Malignancy
  • Nurses with lower extremity problems

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Nurse group
Nurses will be evaluated in terms of burnout, aerobic capacity and musculoskeletal pain.
A stepwise protocol will be used in which the load increases gradually with the bicycle ergometer. In these protocols, the load increases continuously in small amounts throughout the exercise.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Aerobic capacity assessment
Time Frame: up to 30 minutes
A stepwise protocol will be used in which the load increases gradually with the bicycle ergometer. In these protocols, the load increases continuously in small amounts throughout the exercise.
up to 30 minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Burnout assessment
Time Frame: up to 30 minutes
Maslach Burnout Inventory, which was developed by Christina Maslach and Susan Jackson (1986) and Turkish adaptation and validity-reliability study was conducted by Ergin (1992), will be completed. The 7-point Likert-type scale, which consists of 22 items in total and consists of 'Never- Few Times a Year- Few Times a Month- Once a Month- Few Times a Week- Once a Week- Every Day' options in its original form, was reduced to five options in the adaptation study conducted by Ergin (1992) on the grounds that it was not suitable for Turkish culture.
up to 30 minutes
Musculoskeletal evaluation
Time Frame: up to 30 minutes
n 1987, the Nordic Musculoskeletal Questionnaire developed by Kuorinka to measure musculoskeletal pain will be completed. The body is divided into 9 regions: neck, shoulder, back, elbow, hand/wrist, waist, hip/thigh, knee, foot/ankle. It is assessed whether there is a problem in these areas and if so, how long it has been going on
up to 30 minutes

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Songul Baglan Yentur, Firat University

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 (Estimated)

November 10, 2024

Primary Completion (Estimated)

December 10, 2024

Study Completion (Estimated)

December 20, 2024

Study Registration Dates

First Submitted

November 14, 2024

First Submitted That Met QC Criteria

November 15, 2024

First Posted (Estimated)

November 18, 2024

Study Record Updates

Last Update Posted (Estimated)

November 18, 2024

Last Update Submitted That Met QC Criteria

November 15, 2024

Last Verified

November 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • 2024/13-05

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

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.

Clinical Trials on Aerobic Capacity

Clinical Trials on Evaluation of aerobic capacity

Subscribe