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Impact of Physical Activity, Nutritional Status, and Pregnancy-Related Anxiety on Excessive Gestational Weight Gain

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Study Aim

This study aims to observe how physical activity, nutritional status, and pregnancy-related anxiety might influence excessive weight gain during pregnancy.

What is being collected

Data Collection

Collected at a single point in time - Cross-sectional
Who is being recruted

Anxiety Disorders+1

+ Behavior

+ Mental Disorders

From 18 to 45 Years
+6 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Cohort

Tracking disease incidence in order to identify risk factors and understand disease progression over time.
Observational
Study Start: January 2026
See protocol details

Summary

Principal SponsorBezmialem Vakif University
Study ContactAyşe Sena Manzak Dursun, PT, PhD
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: January 2, 2026

Actual date on which the first participant was enrolled.

Excessive weight gain during pregnancy is a significant health issue, as it can lead to complications for both the mother and the newborn. This study focuses on understanding the key factors that contribute to excessive weight gain during pregnancy. These factors include physical activity levels, nutritional habits, and pregnancy-related anxiety. The study aims to identify which of these factors has the most significant impact on excessive gestational weight gain. It involves pregnant women in their third trimester who are being monitored at Gebze Fatih State Hospital. The study is important as it could help improve pregnancy care by identifying ways to manage weight gain effectively, thereby reducing potential health risks for both mother and baby. Participants in this observational study will be asked to complete a series of assessment tools. These include a form to capture demographic details, the Pregnancy Physical Activity Questionnaire (PPAQ) to evaluate physical activity levels, a nutritional status assessment form to examine dietary habits, and a pregnancy-related anxiety questionnaire to measure anxiety levels associated with pregnancy. All participants will receive detailed verbal and written information about the study and will be required to provide written consent before enrollment. The collected data will be analyzed to determine the relative impact of physical activity, nutritional status, and pregnancy-related anxiety on excessive gestational weight gain. The primary outcome of the study is to determine the number of participants with excessive gestational weight gain, as classified by the Institute of Medicine (IOM) recommendations adjusted for pre-pregnancy body mass index.

Official TitleDeterminant Factors in Excessive Gestational Weight Gain: Physical Activity, Nutritional Status, and Anxiety 
Principal SponsorBezmialem Vakif University
Study ContactAyşe Sena Manzak Dursun, PT, PhD
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

150 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Cohort

These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Female

Biological sex of participants that are eligible to enroll.

From 18 to 45 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Anxiety DisordersBehaviorMental DisordersMotor Activity

Criteria

3 inclusion criteria required to participate
Being in the 3rd trimester of pregnancy

Being between 18 and 45 years old

Having the intellectual capacity to understand and respond to what is read.

3 exclusion criteria prevent from participating
High-risk pregnancy

Multiple pregnancy

Having a chronic disease such as a systemic, neurological, orthopedic, etc.

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Recruiting

Bezmialem Vakıf University

Istanbul, Turkey (Türkiye)See the location
Recruiting
One Study Center