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CompletedNCT03247426Updated Nov 29, 2017

Sleep Quality, Job Satisfaction, Quality of Life, Occupational Burnout Levels in Individuals

An observational study in Physical Activity, sponsored by Hacettepe University. Completed at 1 site in Turkey. Open to participants aged 25 Years to 65 Years. Per ClinicalTrials.gov, last updated 2017-11-29.

Sponsored by Hacettepe University · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
109
Ages
25 Years to 65 Years
Sex
All
01

Study summary

The aim of this study is to compare sleep quality, job satisfaction, quality of life, occupational burnout levels among individuals who do or do not do exercise.

Read the detailed description

Physical activity is very important in terms of healthy growth and development, protection from unwanted bad habits, socialization, protection from chronic diseases, and providing an active aging period. At the same time it increases the quality of life throughout life.Especially in individuals who work in sitting position, the risk of physical activity decrease due to intensive working hours, time constraint, social insufficiency is even more risk.Therefore, it is aimed to compare sleep quality, job satisfaction, quality of life, occupational burnout levels among individuals who do or do not do exercise.

02

Conditions studied

  • Physical Activity

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03

In context

Burnout, Professional

214 studies on the registry are indexed under Burnout, Professional; 33 are open to participants now.

This study's enrollment of 109 is below the median of 200 across 53 observational studies indexed under Burnout, Professional.

Browse Burnout, Professional studies →

Lead sponsor

Hacettepe University is the lead sponsor of 983 studies on the registry; 212 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
25 Years to 65 Years
Sexes eligible
All
Sampling method
Probability sample

Study population

Healthy individuals who aged between 25-65 years, are in the profession group working for at least 8 hours, do the same job for at least 5 years, and having no doctor-diagnosed skeletal system disease will be included.

Inclusion criteria

Healthy individuals;

  • Between the ages of 25-65 years,
  • Those who are in the profession group working for at least 8 hours,
  • who do the same job for at least 5 years,
  • Individuals with no doctor-diagnosed skeletal system disease will be included.

Exclusion criteria

Exclusion Criteria:

Individuals;

  • Below the age of 25 years and above the age of 65 years,
  • Individuals with doctor-diagnosed skeletal system disease will be excluded.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
109 participants (actual)
Patient registry
No

Groups and cohorts

  • Evaluation individuals with exercise

    Individuals who work in sitting position and do regular exercises will be recruited.

    Other: Evaluation individuals

  • Evaluation individuals without exercise

    Individuals who work in sitting position and do not perform regular exercises will be recruited.

    Other: Evaluation individuals

Interventions

  • OtherEvaluation individuals

    Sleep quality of the individuals, job satisfaction, quality of life, occupational burnout level will be evaluated.

06

What researchers measure

Primary outcomes

  1. Sleep quality of the individuals

    Pittsburgh Sleep Quality Index (PUKI) will be used to evaluate sleep quality.

    Time frame: 15 days

Secondary outcomes

  1. job satisfaction

    Minnesota Job Satisfaction Scale (MIS) will be used to evaluate job satisfaction.

    Time frame: 15 days

  2. quality of life

    World Health Organization Quality of Life Scale Short Form (WHOQOL-BREF) will be used to evaluate quality of life of the individuals.

    Time frame: 15 days

  3. occupational burnout level

    Maslach Burnout Scale will be used to evaluate occupational burnout.

    Time frame: 15 days

07

Study locations

1 site
  • Hacetttepe University
    Ankara, 06100, Turkey
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 29, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03247426
Lead sponsor
Hacettepe University
Responsible party
SELEN SEREL ARSLAN (Principal Investigator, Hacettepe University) — Principal investigator
First posted
Aug 11, 2017
Start date
Aug 15, 2017
Primary completion
Sep 10, 2017
Completion
Sep 15, 2017
Last update
Nov 29, 2017

Study contacts

SELEN SEREL ARSLAN
principal investigator · Hacettepe University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Nov 2017. You cannot join it, but the record below documents what was studied.

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