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Video coaching for preemies: can a 12-week online program boost motor and cognitive skills?

NCT ID NCT07727720

Symptom relief Sponsor: Izgi Miray Demirbag 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jul 27, 2026 · Last updated Jul 28, 2026 · Updated 1 time

Summary

This study tests whether a 12-week tele-rehabilitation program, called HEP (Homeostasis-Enrichment-Plasticity), can improve motor, cognitive, language, and social-emotional skills in preterm infants born at or before 36 weeks and 6 days. The program involves weekly 45-minute online sessions with a therapist and parent training to support activities at home. Researchers will also measure effects on parental anxiety and goal achievement. The study aims to see if delivering this environmental enrichment-based intervention remotely is feasible and beneficial.

What this could mean

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

Active substance
HEP Tele-Rehabilitation Intervention (Homeostasis-Environmental Enrichment-Plasticity approach)
What this could lead to
If this approach works, it could provide a scalable, home-based early intervention to support development in preterm infants who are at risk for delays.
What could go wrong
This is a small feasibility study with only 16 infants, so results may not apply broadly. The intervention requires consistent parent involvement, which may be challenging for some families.

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

16 people

The number who actually took part.

Started

Nov 2024

Finished

Mar 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.

Ages

4 to 12 months

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: * Infants with a corrected age between 4 and 12 months. * Infants born at or before 36 weeks and 6 days of gestation. * Infants with no congenital anomalies. * Families who agree to participate regularly in the study process. Exclusion Criteria: * Infants with major visual or hearing impairments. * Infants with any genetic syndrome or congenital anomalies. * Infants with medical conditions that prevent active participation in the study (e.g., oxygen dependence). * Infants participating in other experimental rehabilitation studies.

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Conditions

The condition(s) this trial relates to.

Premature Birth

As listed by the trial registrant

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

Preterm

Contacts and locations

Locations

  • Sense On

    Istanbul, Beykoz, 34810, Turkey (Türkiye)

More trials for these conditions

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