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Lying position during baby monitoring affects comfort in obese pregnancies

NCT ID NCT07379307

Symptom relief Sponsor: Tokat Gaziosmanpasa University Source: ClinicalTrials.gov ↗

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at how different body positions during routine fetal monitoring affect pain and comfort in obese pregnant women. 174 women in their third trimester were placed in one of three positions: supported side-lying, unsupported side-lying, or lying on their back. The goal was to find which position offers the most comfort and least pain, helping healthcare providers improve the pregnancy experience for women with obesity.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

174 people

The number who actually took part.

Started

Dec 2023

Finished

Feb 2024

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

19 to 40 years

Sex

Female participants only

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Pregnant women who voluntarily agree to participate in the study * Aged between 19 and 40 years * Experiencing a healthy pregnancy * Gestational age between 28+0 and 40+0 weeks (only third-trimester pregnancies are included, as EFM monitoring is recommended after 27 weeks) * Singleton pregnancy with a live fetus * Body Mass Index (BMI) of 30 or higher * No physical disabilities * Able to speak Turkish to answer questions accurately * No cognitive, comprehension, or communication difficulties Exclusion Criteria: * Pregnant women who do not agree to participate in the study * Aged under 19 years or 41 years and above (adolescent and advanced-age pregnancies are excluded due to increased risk) * Diagnosed with high-risk pregnancy * Illiterate or unable to read/write * Having a contagious disease * Having a mental disorder or history of a mental disorder requiring treatment * Having physical disabilities affecting mobility, hearing, or psychological function * Gestational age less than 28+0 weeks * Currently in active labor

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Conditions

The condition(s) this trial relates to.

Pain Pregnancy in Obesity

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Maternal comfort during fetal monitoring Obesity in pregnancy

Contacts and locations

Locations

  • Tokat State Hospital, Department of Obstetrics and Gynecology, NST Room

    Tokat Province, Tokat Province, 60100, Turkey (Türkiye)

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