Home Visitation Enhancing Linkages Project in Kansas

Sponsor
The National Center on Addiction and Substance Abuse at Columbia University
Study ID
NCT06624332
Status
Not Yet Recruiting

Notify me when recruiting opens

Save your spot on the interest list for this study. We'll keep your details with this study so our team can follow up when recruiting opens.

Not yet recruiting

Add your contact details and location so we can keep your interest tied to this study.

Conditions

Eligibility Criteria

Sex
FEMALE
Age
18 Years - N/A
Healthy Volunteers
Accepted

Interventions

  • e-SBI main session — BEHAVIORAL
    Single 20-minute e-SBI session that includes screening followed by brief motivational intervention.
  • e-SBI Booster Session — BEHAVIORAL
    A 20-minute booster e-SBI session that reinforces content from the main e-SBI session.
  • Text messaging — BEHAVIORAL
    4 weeks of daily automated text messages that reinforce content from the e-SBI main session.

Study Details

The goal of this study is to learn about whether digital screening and brief intervention can help address substance use in postpartum mothers who are enrolled in home visiting programs. The main questions it aims to answer are: 1. What combination of digital intervention components work best for postpartum mothers in home visiting programs? 2. What are the factors that help the intervention work best in home visiting, and what factors serve as barriers to the success of the intervention? Participants in the study will include home visiting staff and postpartum home visiting clients. Participants who are home visitors will be asked to participate in focus groups and interviews, introduce the study to their clients and refer interested clients to the study, complete online surveys, and implement the home visitor components of the intervention with their clients who enroll in the study. Participants who are home visiting clients will be asked to participate in focus groups and interviews, complete online surveys, and complete the digital screening and brief intervention sessions.

Key Dates

First listed
Oct 3, 2024
Start date
Jun 1, 2026
Status verified
Mar 2026
Primary completion
Mar 31, 2027
Completion
Mar 31, 2027

Study Design

Enrollment
120 participants (estimated)
Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT

Arms

  • No Intervention: No intervention Routine HV Only
    Routine home visiting only
  • Experimental: e-SBI main session
    e-SBI main session
  • Experimental: e-SBI main session + booster
    e-SBI main session and e-SBI booster session
  • Experimental: Text messaging only
    text messaging
  • Experimental: e-SBI main session + text messaging
    e-SBI main session Text messaging
  • Experimental: e-SBI main + e-SBI booster + text messaging
    e-SBI main session e-SBI booster session text messaging

Primary Outcome Measure

Substance use [ Time Frame: Assessed at 3-month follow-up and 6-month follow-up ]

Central Contacts

Find similar trials

Related Studies