Midwife support boosts comfort and breastfeeding in new moms

NCT ID NCT07165288

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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 Results may not be published yet.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)
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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

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Status unknown
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First seen Jun 25, 2026 · Last updated Jun 26, 2026 · Updated 1 time

Summary

This study looked at whether giving first-time mothers continuous support from a midwife, starting at 36 weeks of pregnancy through the early weeks after birth, could improve their comfort, sleep quality, and confidence in breastfeeding. 128 women took part, with some receiving extra midwife support and others standard care. The results suggest that this extra support helped women feel more comfortable, sleep better, and feel more confident about breastfeeding.

What this could mean

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

Active substance
continuous midwife support
What this could lead to
If this approach works, it could point toward better support programs for first-time mothers to improve their comfort, sleep, and breastfeeding success.
What could go wrong
This is a small, completed study with 128 participants, so results may not apply to all women. The interventions are supportive, not medical, so benefits are modest and may vary.

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

128 people

The number who actually took part.

Started

Jan 2024

Finished

Dec 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

18 to 36 years

Sex

Female participants only

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

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: All pregnant women who communicate verbally and do not have a reading or writing disability, * Having a singleton healthy pregnancy, * Having a primiparous pregnancy in the 36th week of pregnancy, * Not a midwife by profession, * Not having any diagnosed psychiatric problems were included. Exclusion Criteria: * Women who developed an indication for cesarean section were excluded. For postpartum women; * Those who developed a condition requiring separation from their babies, * Those who wanted to leave the study during the follow-ups, * Those who filled out the data collection forms incompletely, * Those who gave birth before the third interview were excluded.

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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

  • Palu Devlet Hastanesi

    Elâzığ, 23000, Turkey (Türkiye)