Increasing Mothers' Own Milk Feeding in the Neonatal ICU
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Official title
Increasing Human Milk Feeding in the Neonatal ICU
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
The purpose of this study is to adapt, refine, and test the feasibility, acceptability, and implementation of a novel Motivational Interviewing (MI) and Acceptance and Commitment Therapy (ACT) (MIACT) intervention delivered by lactation specialists to increase Black mothers' own milk (MOM) feeding with their infants and to pilot test the efficacy of the MIACT intervention in a sample of Black mothers and their infants to increase MOM-feeding initiation and duration and improve secondary infant and maternal outcomes (e.g., infant length-of-stay, maternal stress), compared to usual lactation support in a neonatal intensive care unit (NICU). The goals of MIACT are to increase mothers' psychological flexibility and motivation for MOM feeding by increasing acceptance and willingness to experience ambivalent and/or uncomfortable thoughts, feelings, and physical sensations related to MOM feeding, with particular attention to the unique needs of Black mothers. Concerns, views, and feelings around MOM feeding will be identified, followed by discussion and practice of acceptance and mindfulness skills. Maternal values will be elicited and goals based on personal values will be set.
Study identification
- NCT ID
- NCT07932652
- Recruitment status
- Recruiting
- Study type
- Interventional
- Phase
- Not applicable
- Enrollment
- 1,176 participants
Conditions and interventions
Interventions
- Motivational Interviewing (MI) and Acceptance and Commitment Therapy (ACT) (MIACT) Behavioral
- Usual Lactation Support Behavioral
Behavioral
Eligibility (public fields only)
- Age range
- 18 Years and older
- Sex
- Female
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Oct 15, 2026 (Actual)
- Primary completion
- Mar 15, 2028 (Estimated)
- Completion
- Jun 15, 2028 (Estimated)
- Last update posted
- Nov 12, 2026
2026 – 2028
United States locations
- U.S. sites
- 1
- U.S. states
- 1
- U.S. cities
- 1
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| The University of Texas Health Science Center at Houston | Houston | Texas | 77030 | Recruiting |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT07932652, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Nov 12, 2026 · Synced Nov 14, 2026
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