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Bringing the Doctor's office to new moms: a van could boost postpartum care

NCT ID NCT07747519

Disease control Sponsor: Women and Infants Hospital of Rhode Island 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 This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Aug 05, 2026 · Last updated Aug 06, 2026 · Updated 1 time

Summary

This trial tests whether offering postpartum checkups in a mobile medical van helps new mothers attend their visits more easily than going to a clinic. About 100 women who gave birth at Women & Infants Hospital will be randomly assigned to receive their standard postpartum care either in the van or at the clinic. Participants will complete their checkup and fill out short surveys about their experience. The goal is to see if the van improves attendance and satisfaction with postpartum care.

What this could mean

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

Active substance
Mobile postpartum care delivered in a medical van versus standard clinic care
What this could lead to
If mobile van visits improve attendance and satisfaction, this could offer a more accessible model for postpartum care, potentially reducing missed checkups.
What could go wrong
This is a small pilot study, so results may not apply broadly. The van's service area limits who can participate, and feasibility may not translate to larger settings.

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

About 100 people

The number the study aims to enrol. It can still change while the study runs.

Started

Jun 2026

Expected to finish

Jun 2027

An estimate. End dates often move.

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

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: * Age 18 years or older * Delivered a live infant at Women \& Infants Hospital * Reside within the geographic area serviced by the mobile van * Plans to remain in the area for at least 3 months postpartum * Able to provide informed consent Exclusion Criteria: * Severe maternal medical complications requiring prolonged inpatient postpartum care (e.g., ICU stay beyond routine recovery) * Plans to relocate outside the mobile van service area within 3 months postpartum * Cognitive impairment or psychiatric conditions that would interfere with the ability to provide informed consent or participate in study procedures * Participation in another postpartum intervention study that may influence visit attendance or care delivery

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Conditions

The condition(s) this trial relates to.

puerperal disorder

As listed by the trial registrant

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

Neonatal Postpartum

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    The full official record for this study. This one lists no contact details, but it is the first place any would appear.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Women & Infants Hospital of Rhode Island

    Providence, Rhode Island, 02905, United States

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