Exercise Benefits and Barriers in Pregnancy

NCT ID: NCT07134959

Last Updated: 2026-01-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

300 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-09-01

Study Completion Date

2025-12-01

Brief Summary

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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.

Detailed Description

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Regular physical activity (PA) and exercise during pregnancy help protect the health of both the mother and the baby by reducing the risk of excessive gestational weight gain, hypertension, gestational diabetes, venous problems, and birth-related complications. They also have positive effects on sleep, stress, anxiety, depression, and overall quality of life. However, PA participation rates during pregnancy are low and tend to decline as pregnancy progresses through the trimesters. Hormonal and physiological changes, weight gain, fatigue, and psychological disturbances are among the main factors limiting participation. Therefore, identifying the barriers to PA during pregnancy and developing strategies to address them is essential. Assessing perceptions of the benefits and barriers to exercise can guide interventions aimed at increasing PA levels. This study aims to determine the validity and reliability of the Exercise Benefits/Barriers Scale in pregnant women, with the expectation that its findings will provide valuable evidence for both scientific research and clinical practice.

Conditions

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Pregnancy

Study Design

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Observational Model Type

OTHER

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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study group

pregnant women

No interventions assigned to this group

control group

healthy non-pregnant women

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

1. Being between 18 and 45 years of age,
2. Being in the second or third trimester of pregnancy,
3. Being literate in Turkish,
4. Willingness to participate in the study.


1. Being between 18 and 45 years of age,
2. Female sex,
3. Being literate in Turkish,
4. Willingness to participate in the study.

Exclusion Criteria

1. Presence of pregnancy complications that may prevent physical activity and exercise (e.g., preeclampsia, vaginal bleeding, heart disease),
2. Presence of orthopedic or neurological problems that may hinder participation in the study,
3. Presence of visual, auditory, or cognitive impairments severe enough to prevent participation in the study,
4. Multiple pregnancy.


1. Having a disease severe enough to prevent physical activity and exercise (e.g., endocrine and metabolic disorders, cardiopulmonary diseases),
2. Presence of orthopedic or neurological problems that may hinder participation in the study,
3. Presence of visual, auditory, or cognitive impairments severe enough to prevent participation in the study,
4. Participation in another experimental or drug study during the study period,
5. Being pregnant or suspected of pregnancy,
6. Having experienced pregnancy, childbirth, or surgical intervention within the last six months.
Minimum Eligible Age

18 Years

Maximum Eligible Age

45 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Ordu University

OTHER

Sponsor Role lead

Responsible Party

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Semiha Yenişehir

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Semiha Yenişehir

Role: PRINCIPAL_INVESTIGATOR

Ordu University

Locations

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Ordu Üniversitesi

Ordu, Altınordu, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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E-1146814

Identifier Type: -

Identifier Source: org_study_id

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