- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06693206
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
Intervention / Treatment
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
- Name: Songul Baglan Yentur
- Phone Number: +90 4242370000
- Email: songulbaglan23@hotmail.com
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.
Sponsor
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
Keywords
Additional Relevant MeSH Terms
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.
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