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Development of a scale to measure quality of life of overweight women

  • Yeter Kitiş
  • Filiz HisarEmail author
  • Kemal Macit Hisar
Original Article
  • 54 Downloads

Abstract

Purpose

This study presents the results of methodological research that derives evaluation items and tests the validity and reliability of the scale to measure quality of life of the overweight women.

Methods

The scale items were developed by the current researchers directly from the consultation data following a group interviewing process aiming to capture the women’s experiences, who are currently receiving primary health care. Pretest interviews were used to ensure that the questions were understood correctly. Six experts determined items for content validity of the scale and the evaluations of experts were scored using a content validity index. The scale is a Likert-type scale, ranging from 1 to 5. The items were tested on a sample of 506 healthy women. The body mass indices of participants were 30 and above. Psychometric analyses included explanatory factor analysis (EFA) and item response theory. Parallel analysis was used to extract factors in EFA. Internal consistency and Spearman Brown split-half test correlation were used for testing reliability.

Results

The scale was refined as four final dimensions, comprising 40 items as a whole. The result of Bartlett’s Test of Sphericity was found sufficient (χ2 = 14164.92; p < 0.001) and the KMO value was 0.959. This statistically significant value (p < 0.001) indicates that the sampling was sufficient and data had normal distribution. Cronbach’s alpha was 0.967. The Spearman Brown coefficient was found to be 0.884.

Conclusion

It was found that the scale is a valid and reliable assessment tool that can be used to measure the quality of life of overweight women.

Level of evidence

Methodological study, Level V.

Keywords

Scale Overweight women Quality of life Public health Turkey 

Notes

Compliance with ethical standards

Conflict of interest

There was no conflict of interest.

Ethical approval

The ethical consent that is required for the performance of the research was obtained from the Ethics Committee Gazi University; before the data were collected institutional permissions were obtained.

Informed consent

The women were asked to read the explanations related to the study on the front page of the questionnaire and to complete the questionnaire if they wished to participate in the study. After that, verbal and written consent were obtained from participants.

Data availability

The data used to generate the results of this manuscript are available on request from corresponding author.

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Copyright information

© Springer Nature Switzerland AG 2019

Authors and Affiliations

  1. 1.Faculty of Health Science, Department of NursingGazi UniversityAnkaraTurkey
  2. 2.Nursing FacultyNecmettin Erbakan UniversityKonyaTurkey
  3. 3.Department of Public Health, Faculty of MedicineSelcuk UniversityKonyaTurkey

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