Video calls may ease the stress of having a newborn in intensive care

NCT ID NCT06252883

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Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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 Jul 13, 2026 · Last updated Jul 14, 2026 · Updated 1 time

Summary

This study tests whether giving parents of NICU babies regular video calls (2-3 times a week) in addition to standard phone updates can reduce their stress and anxiety. Half of the parents receive the video calls; the other half get only routine updates. Stress levels are measured through questionnaires over an 8-week period. The goal is to see if seeing their baby on video helps parents feel more connected and less anxious.

What this could mean

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

Active substance
serial bedside video call communication via Doximity app on iPad
What this could lead to
If effective, regular video calls could become a simple, low-cost way to ease stress and strengthen bonding for parents of hospitalized newborns.
What could go wrong
This is a small, early-stage study (70 participants) at a single center, so results may not apply widely. Stress is subjective and questionnaires may not capture all effects.

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 70 people

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

Started

Jun 2024

Expected to finish

Apr 2027

An estimate. End dates often move.

Lead sponsor

A government agency

The lead sponsor is a government body.

Who can take part

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

Ages

7 to 60 days

Sex

Anyone

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: \- Newborns with 7 days or more of NICU stay Exclusion Criteria: Infant with * intrauterine drug exposure * major critical congenital cardiac anomaly * major neurologic anomaly * chromosomal disorder.

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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.

How to take part

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  1. The places running it

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

  2. The official record

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  3. A doctor treating you

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Contacts and locations

Locations

  • John H. Stroger Hospital of Cook County

    RECRUITING

    Chicago, Illinois, 60612, United States

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