Obesity Awareness, Physical Activity Level and Sedentary Behavior in Obese Women

November 15, 2022 updated by: Buket AKINCI, Biruni University

Investigation of the Relationship of Obesity Awareness With Physical Activity Level and Sedentary Behavior in Obese Women

It is known that the incidence of obesity, which is a global health problem, is higher in women. The aim of this study is to examine the relationship of obesity awareness with physical activity level and sedentary behavior in obese women.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Obese people are at risk for medical conditions that can lead to greater morbidity and mortality. It is known that the incidence of obesity, which is a global health problem, is higher in women. Lack of physical activity and sedentary behavior are well-known risk factors for obesity and the relationship between them has been supported by many studies. As a matter of fact, some studies have reported that public health programs should focus on increasing individuals' physical activity levels as well as reducing sitting time. While examining the sedentary behavior and physical activity levels of obese women, evaluating their obesity awareness status, can facilitate increasing their awareness of the disease, initiating and complying with treatment. The aim of this study is to examine the relationship of obesity awareness with physical activity level and sedentary behavior in obese women.

Study Type

Observational

Enrollment (Actual)

82

Contacts and Locations

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

Study Locations

      • Istanbul, Turkey, 34000
        • Bezmi Alem Vakıf University

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

14 years to 61 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Sampling Method

Probability Sample

Study Population

The study will consist of 70 obese women volunteers aged between 18-65 years.

Description

Inclusion Criteria:

  • The women who are ages between 18-65 years,
  • BMI ≥ 30.0 kg/m2 according to WHO classification.

Exclusion Criteria:

  • BMI < 30.0 kg/m2 according to WHO classification,
  • Male participants,
  • Inability to cooperate with assessments,
  • Those who have had severe trauma or surgery that limit physical activities in the last 6 months,
  • Those who have orthopedic, neurological, cardiovascular problems that limit / prevent ambulation,
  • Pregnancy or suspected pregnancy,
  • Individuals are included in a rehabilitation program.

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

  • Observational Models: Cohort
  • Time Perspectives: Cross-Sectional

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
obese women
The study will consist of 70 obese women volunteers aged between 18-65 years.
Obesity awareness, physical activity, and sedentary time questionnaires will be applied to these cases.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Obesity Awareness
Time Frame: baseline
Obesity awareness will be measured by Obesity Awareness Insight Scale and Obesity.
baseline

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Sedentary Behavior Questionnaire
Time Frame: baseline
It is a questionnaire developed to evaluate the time spent performing 9 sedentary behaviors on a normal weekday and weekend day. The questionnaire has nine different response options. For the total score, the durations of the behaviors in hours are added separately as weekdays and weekends. To obtain the average sedentary behavior times for weekdays and weekends, the total duration of the week is multiplied by 5, and the total duration of the weekend is multiplied by 2.
baseline
International Physical Activity Questionnaire Short Form
Time Frame: baseline
The questionnaire allows calculation of metabolic equivalent (MET) by measuring frequency, duration and physical activity intensity level in the last seven days and shows weekly physical activity amount. It is calculated as weekly working hours (MET-min/week). Physical activity levels of individuals according to the calculated MET value: (1) <600 MET-min/week not active (sedentary, inactive), (2) 600-3000 MET-min/week minimally active, and (3) >3000 MET-min/week very active (physical activity that increases well-being) classified as.
baseline
Waist circumference
Time Frame: baseline
Waist circumference will be measured with a tape measure in the standing position, by determining the midpoint between the lowest rib and the iliac crest from the exposed waist circumference.
baseline
Body fat-muscle ratios
Time Frame: baseline
These measurements will be determined by bioelectrical impedance.
baseline

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 (Actual)

September 20, 2022

Primary Completion (Actual)

November 15, 2022

Study Completion (Actual)

November 15, 2022

Study Registration Dates

First Submitted

September 9, 2022

First Submitted That Met QC Criteria

September 9, 2022

First Posted (Actual)

September 13, 2022

Study Record Updates

Last Update Posted (Actual)

November 16, 2022

Last Update Submitted That Met QC Criteria

November 15, 2022

Last Verified

November 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • 2022/71-12

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Undecided

IPD Plan Description

If the journal asks for the data, we will share it.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

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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