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
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Conditions
Eligibility Criteria
- Sex
- FEMALE
- Age
- 18 Years - N/A
- Healthy Volunteers
- Accepted
Interventions
- e-SBI main session — BEHAVIORALSingle 20-minute e-SBI session that includes screening followed by brief motivational intervention.
- e-SBI Booster Session — BEHAVIORALA 20-minute booster e-SBI session that reinforces content from the main e-SBI session.
- Text messaging — BEHAVIORAL4 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 OnlyRoutine home visiting only
- Experimental: e-SBI main sessione-SBI main session
- Experimental: e-SBI main session + boostere-SBI main session and e-SBI booster session
- Experimental: Text messaging onlytext messaging
- Experimental: e-SBI main session + text messaginge-SBI main session Text messaging
- Experimental: e-SBI main + e-SBI booster + text messaginge-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
- Sarah Dauber, PhD212-841-5270
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