The Effect of Exercise-Oriented Training on Physical Activity Level and Exercise Awareness in Overweight and Obese Women

Sponsor
Ataturk University (Other)
Overall Status
Completed
CT.gov ID
NCT06123273
Collaborator
(none)
112
1
2
7
16.1

Study Details

Study Description

Brief Summary

This study aimed to investigate the effect of an exercise-oriented training on physical activity level and exercise awareness in overweight and obese women. Participants will randomized into intervention group (IG) and control group (CG) and followed-up for three months. The International Physical Activity Questionnaire Short Form (IPAQ) will be applied to both groups at the beginning and end of the study to determine the level of physical activity, and the Exercise Health Belief Model Scale (EHBM) will be applied to evaluate the exercise awareness level, and anthropometric measurements (weight, body mass index, waist circumference) will recorded. The CG will receive no other interventions other than routine recommendations. The IG will be given face-to-face training to increase exercise awareness along with routine recommendations after the first meeting, and they will be contacted by phone every two weeks for three months.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Exercise-oriented training
N/A

Detailed Description

Obesity and insufficient physical activity are among the most important health problems of today. Both obesity and physical inactivity are risk factors for many chronic diseases. This study aimed to investigate the effect of an exercise-oriented training on physical activity level and exercise awareness in overweight and obese women. Participants (n=112) were randomized into intervention group (IG) and control group (CG) and followed-up for three months. The International Physical Activity Questionnaire Short Form (IPAQ) was applied to both groups at the beginning and end of the study to determine the level of physical activity, and the Exercise Health Belief Model Scale (EHBM) was applied to evaluate the exercise awareness level, and anthropometric measurements (weight, body mass index, waist circumference) were recorded. The CG received no other interventions other than routine recommendations. The IG was given face-to-face training to increase exercise awareness along with routine recommendations after the first meeting, and they were contacted by phone every two weeks for three months.

Study Design

Study Type:
Interventional
Actual Enrollment :
112 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
The Effect of Exercise-Oriented Training on Physical Activity Level and Exercise Awareness in Overweight and Obese Women: A Randomized-Controlled Trial
Actual Study Start Date :
Aug 1, 2021
Actual Primary Completion Date :
Feb 1, 2022
Actual Study Completion Date :
Mar 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention group

The intervention group was given an exercise-oriented training

Behavioral: Exercise-oriented training
IG received an exercise-oriented training with a 20-minute presentation including graphics, in line with clinical guidelines, in addition to routine recommendations. The training included information about the benefits of exercise and the harms of a sedentary life, the relationship between exercise and chronic diseases, suggestions to have a more active lifestyle and on how to exercise, the duration and form of exercise necessary for a healthy life, and the things to be considered while exercising. During the three-month follow-up, the subjects in the IG were called every two weeks to ask about their weight measurements, their level of exercise, and how much they walked. The subjects' questions, if any, were answered, and the interview was completed by making exercise suggestions.
Other Names:
  • close follow-up
  • No Intervention: Control group

    The control group was given only routine recommendations

    Outcome Measures

    Primary Outcome Measures

    1. The International Physical Activity Questionnaire Short Form was used to determine the physical activity level at the beginning and end of the study [3 months]

      The International Physical Activity Questionnaire Short Form was used to determine the physical activity level at the beginning and end of the study. The minimum score is <600 Maximal Exercise Test (MET) -minute/week while the maximum score is >3000 MET-minute/week . High score means high exercise belief.

    Secondary Outcome Measures

    1. Exercise Health Belief Model Scale [3 months]

      Exercise Health Belief Model Scale was used to evaluate the exercise awareness levels of all participants. The minimum score is 25 while the maximum score is 125. High score means high exercise belief.

    2. Anthropometric measure [3 months]

      Body Mass Index was used as an anthropometric measurement. All of the participants were recorded . It is measured as weight in kilograms divided by height in meters squared.

    3. Body fat [3 months]

      body fat percentage were recorded.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • BMI 25-34.9 g/m2

    • Female

    • Turkish

    Exclusion Criteria:
    • Individuals with disabilities to exercise

    • pregnant/breastfeeding women

    • Individuals with Stage 2-3 obesity (BMI >35 kg/m2)

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Ataturk University Hospital Erzurum Turkey 25040

    Sponsors and Collaborators

    • Ataturk University

    Investigators

    • Principal Investigator: Zehranur Kacar, Ataturk University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Yasemin Cayir, Head of Department of Family Medicine, Ataturk University
    ClinicalTrials.gov Identifier:
    NCT06123273
    Other Study ID Numbers:
    • TTU-2021-9585
    First Posted:
    Nov 8, 2023
    Last Update Posted:
    Nov 8, 2023
    Last Verified:
    Nov 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 8, 2023