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Home visits for pregnant women: a simple way to better births?

NCT ID NCT04628598

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 looked at whether home visits by healthcare providers during pregnancy can improve mothers' knowledge, increase vaginal births, boost breastfeeding confidence, and reduce postpartum depression. Sixty-four first-time mothers with low-risk pregnancies took part. The approach involved providing prenatal education and care in the women's own homes.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
home visits with prenatal education
What this could lead to
If successful, this could show that home visits help pregnant women learn more and have better birth outcomes.
What could go wrong
This is a small, completed study with only 64 participants, so results may not apply to everyone. It does not test a new drug or treatment.

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

64 people

The number who actually took part.

Started

Nov 2020

Finished

Feb 2022

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

18 years and older

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: * The pregnant woman is primiparas. * Detection of the pregnant woman in family medicine software * The pregnant woman does not have a high risk pregnancy. * Finding a single fetus in the pregnant woman. * Not having received infertility treatment. * The pregnant woman did not have a psychiatric diagnosis. * The pregnant woman's acceptance to participate in the research. Exclusion Criteria: * Being in the high risk category of the pregnant woman * The mother tongue is not Turkish * Having attended a planned, periodic pregnancy school course * Being multiparous

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

Contacts and locations

Locations

  • İstanbul Üniversitesi Cerrahpaşa

    Istanbul, Avcılar, 34320, Turkey (Türkiye)

More trials for these conditions

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