Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Cure My Disease

Don't miss your cure!

 Log in / Sign up

Could your sleep and screen time impact labor? new study investigates

NCT ID NCT07299708

Knowledge-focused Sponsor: Tepecik Training and Research Hospital Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 followed 127 first-time mothers to see if their sleep quality, anxiety levels, and nighttime phone use before labor were linked to how long labor lasted and whether they needed extra medical help. Participants filled out questionnaires during routine checkups, and researchers tracked their labor progress from hospital admission to birth. The goal was to understand if these everyday factors might play a role in childbirth.

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.

Participants

127 people

The number who actually took part.

Started

Aug 2025

Finished

Nov 2025

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.

Who is studied

This study population consists of term primiparous pregnant women who attended routine antenatal follow-up at Izmir Tepecik Training and Research Hospital and subsequently experienced spontaneous onset of labor. All participants were healthy, low-risk obstetric patients with singleton, cephalic presentations and no medical or obstetric complications.

Ages

18 to 50 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 at ≥ 37 weeks of gestation * Completion of PSQI (sleep quality) and BAI (anxiety) assessments during antenatal clinic visit * Singleton pregnancy * Cephalic presentation * Age 18 to 50 years * Planning to deliver at the study hospital * Able to provide informed consent Exclusion Criteria: * Multiple pregnancy * Non-cephalic presentation * Delivery occurring at another hospital or birth center * Elective planned cesarean delivery * Major fetal anomaly * Placenta previa or placenta accreta spectrum * Preeclampsia, eclampsia, HELLP syndrome * Gestational diabetes requiring insulin * Chronic medical disorders affecting labor physiology * Use of sedative, hypnotic, or psychotropic medications * Inability to complete questionnaires

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Labor progression are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

Conditions

The condition(s) this trial relates to.

anxiety disorder insomnia

As listed by the trial registrant

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

Labor progression Pregnancy

Contacts and locations

Locations

  • Tepecik Training and Research Hospital

    Izmir, 35020, Turkey (Türkiye)

More trials for these conditions

Other studies related to the condition(s) this trial covers.