Ultrasound and guidance help pregnant women with addiction get care
NCT ID NCT05814575
First seen Jun 25, 2026 · Last updated Sep 18, 2026 · Updated 5 times
Summary
This study tested a program that combines community-based fetal ultrasound with care navigation to help pregnant women with substance use disorder engage in prenatal care and substance use treatment. The program used motivational interviewing and strength-based education to support mothers. 103 pregnant women participated, and the study measured retention, maternal-fetal attachment, and use of prenatal and substance use treatment services.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- behavioral intervention (fetal ultrasound with motivational interviewing and care navigation)
- What this could lead to
- If successful, this approach could improve prenatal care and substance use treatment engagement for pregnant women with substance use disorder, potentially leading to better health outcomes for mothers and babies.
- What could go wrong
- This is a small, completed exploratory study (103 participants) without a control group, so results may not be generalizable. The intervention is behavioral and may not work for everyone.
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
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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
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103 people
The number who actually took part.
- Started
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Jun 2023
- Finished
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Nov 2025
- Lead sponsor
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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
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18 to 45 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide 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: * Pregnant persons, Aged 18 through 45, between 22-32 weeks gestation at study entry * Provision of signed and dated informed consent form * Not incarcerated * Able to read and understand English * For infants after delivery, parental informed consent to participate in the study * Stated willingness to comply with all study procedures * Meets Diagnostic and Statistical Manual 5 criteria for Substance Abuse or substance use disorder in the last 12 months or is in active treatment for substance use disorder (including Nicotine/Tobacco, alcohol, marijuana, illicit and licit substances, and opioids) or actively using substances during pregnancy. * Willingness to participate in the NEXUS regimen Exclusion Criteria: * Presenting with cognitive impairment * psychiatric instability (active psychosis or acute mania) * language or legal barriers that would limit the patient's ability to provide informed consent and complete research assessments. * Known fetal anomalies * Medical conditions requiring frequent ultrasound monitoring outside the study (e.g. Gestational Diabetes)
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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
-
Virginia Commonwealth University
Richmond, Virginia, 23298, United States
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