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OpenTrials
Completed

NCT Number: NCT07001020

Innovating Technology Solutions for Residents in Support Housing Communities w SUD Through Community-Engaged Research

The goal of this clinical trial is to understand whether a technology-based solution, provided to residents in permanent supportive housing, is acceptable, feasible to implement, and has promise for improving resident stability. The main questions it aims to answer are:

• Is the technology-based, community-defined solution usable, acceptable, feasible, and have promise of effectiveness for improving resident knowledge?

There is no comparison group, all participants will receive the technology-based intervention. Researchers expect the intervention will include 2 weeks of intervention content that includes videos and incentives for completing content though the solution tested will ultimately be co-defined by our community board.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Oregon Research Behavioral Intervention Strategies, Inc.

Springfield, Oregon, 97477-2019, United States

About this study

Our clinical trial is a pre-post assessment of resident knowledge.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Residents:

  • 18 and older;
  • past or current resident in supportive housing community;
  • past or current elevated substance use

Staff:

  • 18 or older;
  • staff at partner agency

Treatment and study plan

Technology-based Intervention

Behavioral

Technology-based intervention co-developed by a community board.

Primary outcomes

  1. Knowledge

    Time frame: baseline; 30 days

    Knowledge is gain in knowledge related to Cognitive Behavioral Therapy (CBT) skills and life skills taught by the intervention as the number of items answered correctly.

  2. Self-efficacy

    Time frame: baseline; 30 days

    Self-efficacy will assess participant confidence in their ability to implement the skills learned from the intervention. We will develop the items as part of the study, and items will be identified based on the CBT principles and skill applications taught in the program. We will use a 5-point Likert scale of not at all confident (=1) to very confident (=5). A mean score will be computed, ranging from 1 to 5, with higher scores indicating greater self-efficacy in implementing the skills learned in the intervention.

  3. Behavioral intentions

    Time frame: baseline; 30 days

    Behavioral intentions are participants' self-reported likelihood of implementing the skills learned from the intervention on a regular basis. We will develop the items as part of the study, and items will be identified based on the CBT principles and skill applications taught in the program. We will use a 5-point Likert scale of not at all likely (=1) to very likely (=5). A mean score will be computed, ranging from 1 to 5, with higher scores indicating a greater likelihood of implementing the skills learned in the intervention on a regular basis.

Other outcomes

  1. Dosage

    Time frame: Through study completion, an average of 1 month

    Dosage is the number of sessions and skills practices a participant completes

Sponsors and collaborators

Lead sponsor

Oregon Research Behavioral Intervention Strategies, Inc.

Industry

Collaborators

  • National Institute on Drug Abuse (NIDA)

Registry information

Official study title

Innovating Technology Solutions for Residents in Supportive Housing Communities With SUD Through Community-Engaged Research

Acronym: HousingSUD

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Jun 3, 2025
Registry last updated
Jul 13, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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