Exercise Benefits and Barriers in Pregnancy
Validity and Reliability of Turkish Version Exercise Benefits/Barriers Scale in Pregnant Women
1 other identifier
observational
300
1 country
1
Brief Summary
The aim of this study is to examine the validity and reliability of the Exercise Benefits/Barriers Scale in pregnant women. It will contribute to raising awareness about engaging in physical activity and exercise during pregnancy in the pregnant population through the applied questionnaires.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Sep 2025
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 14, 2025
CompletedFirst Posted
Study publicly available on registry
August 21, 2025
CompletedStudy Start
First participant enrolled
September 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 25, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2025
CompletedJanuary 22, 2026
January 1, 2026
3 months
August 14, 2025
January 20, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Exercise Benefits/Barriers Scale (EBBS):
Developed in 1987 by Sechrist et al. to assess individuals' perceptions of the benefits of and barriers to exercise (Sechrist et al., 1987). It is a Likert-type scale with responses rated from "4 = strongly agree" to "1 = strongly disagree." The scale consists of two subscales: EBBS-Benefits and EBBS-Barriers. The EBBS-Benefits subscale contains 29 items, while the EBBS-Barriers subscale contains 14 items. In the EBBS-Barriers subscale, lower scores indicate a higher perceived barrier to exercise, whereas in the EBBS-Benefits subscale, higher scores indicate a more positive perception of exercise. The validity and reliability of the Turkish version were demonstrated by Saraç et al. (2024), with Cronbach's alpha coefficients of 0.95 for the EBBS-Benefits subscale and 0.82 for the EBBS-Barriers subscale (Saraç et al., 2024).
At baseline and 5 days after the first assessment
Secondary Outcomes (5)
Barriers to Physical Activity During Pregnancy Scale
at baseline
Pregnancy Physical Activity Questionnaire (PPAQ)
at baseline
International Physical Activity Questionnaire-Short Form (IPAQ-SF)
at baseline
Pregnancy Exercise Self-Efficacy Questionnaire
at baseline
Visual Analog Scale (VAS) for Kinesiophobia
at baseline
Study Arms (2)
study group
pregnant women
control group
healthy non-pregnant women
Eligibility Criteria
Ordu University Training and Research Hospital
You may qualify if:
- Being between 18 and 45 years of age,
- Being in the second or third trimester of pregnancy,
- Being literate in Turkish,
- Willingness to participate in the study.
You may not qualify if:
- Presence of pregnancy complications that may prevent physical activity and exercise (e.g., preeclampsia, vaginal bleeding, heart disease),
- Presence of orthopedic or neurological problems that may hinder participation in the study,
- Presence of visual, auditory, or cognitive impairments severe enough to prevent participation in the study,
- Multiple pregnancy.
- Being between 18 and 45 years of age,
- Female sex,
- Being literate in Turkish,
- Willingness to participate in the study.
- Having a disease severe enough to prevent physical activity and exercise (e.g., endocrine and metabolic disorders, cardiopulmonary diseases),
- Presence of orthopedic or neurological problems that may hinder participation in the study,
- Presence of visual, auditory, or cognitive impairments severe enough to prevent participation in the study,
- Participation in another experimental or drug study during the study period,
- Being pregnant or suspected of pregnancy,
- Having experienced pregnancy, childbirth, or surgical intervention within the last six months.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Ordu Universitylead
Study Sites (1)
Ordu Üniversitesi
Ordu, Altınordu, 52000, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Semiha Yenişehir
Ordu University
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- CROSS SECTIONAL
- Target Duration
- 5 Days
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
August 14, 2025
First Posted
August 21, 2025
Study Start
September 1, 2025
Primary Completion
November 25, 2025
Study Completion
December 1, 2025
Last Updated
January 22, 2026
Record last verified: 2026-01
Data Sharing
- IPD Sharing
- Will not share