Home Visitation Enhancing Linkages Project in Kansas
Starting soon · Not applicable
Conditions studied: Substance Use
In brief
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 facts
- Study ID
- NCT06624332
- Run by
- The National Center on Addiction and Substance Abuse at Columbia University
- People needed
- 120
- Starts
- 2026-06-01
- Expected to finish
- 2027-03-31
- Last updated by the study team
- 2026-03-18
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- English-speaking
- Age 18 years old or older
- Gave birth to a baby within the prior year
- Enrolled in a Healthy Families Kansas program with a participating home visitor
- Not currently enrolled in substance use treatment
You may not qualify if…
- Does not speak English
- Under age 18 years
- Did not give birth to a baby within the prior year
- Not enrolled in a Healthy Families Kansas program with a participating home visitor
- Currently enrolled in substance use treatment
Full record on ClinicalTrials.gov
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