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NCT03165565 · ClinicalTrials.gov registry record · NA

Facilitating Treatment Entry and Family Planning in Substance-using Neonatal Intensive Care Unit (NICU) Mothers

A NA study, sponsored by The University of Texas Health Science Center, Houston.

Completed
Registry status
NA
Development phase
64
Enrollment target

NCT03165565 is a NA study that has completed, run by The University of Texas Health Science Center, Houston. The registered enrollment target is 64 participants.

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The verdict

NCT03165565, a NA study, has completed, sponsored by The University of Texas Health Science Center, Houston.

COMPLETED
Registry status
NA
Development phase
64 participants
Enrollment target

Study Summary

The purpose of this pilot study is to assess whether the hospital-based, adaptive behavioral intervention strategy promotes treatment entry and reduces risk of additional substance-exposed pregnancies (SEPs), as well as HIV and Hepatitis C Virus (HCV) risks among substance-using NICU mothers. Additionally, to assess whether the intervention increases use of professional obstetrical/gynecological resources for contraception to reduce substance-exposed pregnancies (SEPs).

Interventions

  • BEHAVIORAL Motivational Interviewing (MI) and Acceptance and Commitment Therapy (ACT)
  • BEHAVIORAL Conventional Care

Trial Details

FieldValue
Enrollment Target 64 participants
Start Date 2017-07-05
Est. Completion 2020-01-03
Phase NA

What the Registry Record Tells You About NCT03165565

The ClinicalTrials.gov registry entry for NCT03165565 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 64 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is The University of Texas Health Science Center, Houston, which has 732 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Motivational Interviewing (MI) and Acceptance and Commitment Therapy (ACT) is the first listed.

NCT03165565 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT03165565 about?

NCT03165565 is a clinical study titled "Facilitating Treatment Entry and Family Planning in Substance-using Neonatal Intensive Care Unit (NICU) Mothers". The purpose of this pilot study is to assess whether the hospital-based, adaptive behavioral intervention strategy promotes treatment entry and reduces risk of additional substance-exposed pregnancies (SEPs), as well as HIV and Hepatitis C Virus (HCV) risks among substance-using NICU mothers. Additi...

What is the current status of trial NCT03165565?

This trial is currently completed. It is a NA study. The enrollment target is 64 participants. The study started on 2017-07-05. Estimated completion is 2020-01-03.

What interventions are being tested in trial NCT03165565?

The interventions under investigation include: Motivational Interviewing (MI) and Acceptance and Commitment Therapy (ACT) (BEHAVIORAL), Conventional Care (BEHAVIORAL).

Who is sponsoring clinical trial NCT03165565?

This trial is sponsored by The University of Texas Health Science Center, Houston, which has 732 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.