NCT07001020

Brief Summary

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.

Trial Health

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Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
25

participants targeted

Target at below P25 for not_applicable

Timeline
1mo left

Started Apr 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress60%
Apr 2026Jun 2026

First Submitted

Initial submission to the registry

May 21, 2025

Completed
13 days until next milestone

First Posted

Study publicly available on registry

June 3, 2025

Completed
10 months until next milestone

Study Start

First participant enrolled

April 1, 2026

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2026

Last Updated

March 6, 2026

Status Verified

March 1, 2026

Enrollment Period

2 months

First QC Date

May 21, 2025

Last Update Submit

March 4, 2026

Conditions

Keywords

eviction, housing stability, training

Outcome Measures

Primary Outcomes (3)

  • Knowledge

    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.

    baseline; 30 days

  • Self-efficacy

    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.

    baseline; 30 days

  • Behavioral intentions

    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.

    baseline; 30 days

Other Outcomes (1)

  • Dosage

    Through study completion, an average of 1 month

Study Arms (1)

Intervention

EXPERIMENTAL

All participants will be assigned to the intervention, which includes exposure to the technology-based solution while participants are housed within permanent supportive housing. It is anticipated that the intervention will deliver a total of 10 sessions of harm reduction focused cognitive behavioral skills and skills applications. A total of 20 skills practice sessions are also included. Financial incentives are provided up to $50 for completion of sessions and skills practice.

Behavioral: Technology-based Intervention

Interventions

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

Intervention

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Residents: 1. 18 and older; 2. past or current resident in supportive housing community; 3. past or current elevated substance use Staff: 1. 18 or older; 2. staff at partner agency

Contact the study team to discuss eligibility requirements. They can help determine if this study is right for you.

Sponsors & Collaborators

Study Sites (1)

Oregon Research Behavioral Intervention Strategies, Inc.

Springfield, Oregon, 97477-2019, United States

Location

MeSH Terms

Conditions

Substance-Related DisordersHarm Reduction

Condition Hierarchy (Ancestors)

Chemically-Induced DisordersMental DisordersBehavior

Study Officials

  • David R Smith, PhD

    Oregon Research Behavioral Intervention Strategies, Inc.

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
SINGLE GROUP
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

May 21, 2025

First Posted

June 3, 2025

Study Start

April 1, 2026

Primary Completion (Estimated)

June 1, 2026

Study Completion (Estimated)

June 1, 2026

Last Updated

March 6, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will share

Data will be collected from 25 participants, generating 1 dataset with two assessment time points (baseline, 1-month post-enrollment) including information on participant demographics, knowledge, self-efficacy, and planned behavior. Raw data will be transformed using SPSS and used for statistical analysis. Participant identities, and individual de-identified data will be made available for sharing. All quantitative experimental data produced during the course of the project will be preserved and shared. To facilitate interpretation of the data, a data dictionary, statistical analysis plans, and data collection instruments will be created, shared, and associated with the relevant datasets. Aggregate clinical trials data from all arms of the study will be available in clinicaltrials.gov, along with related metadata. All other data described above in the "data to be shared" section will be deposited into the openICPSR repository.

Shared Documents
STUDY PROTOCOL, SAP, ICF
Time Frame
Shared data generated from this project will be made available as soon as possible, and no later than the time of publication or the end of the funding period, whichever comes first. The duration of preservation and sharing of the data will be a minimum of 5 years after the end of the funding period.
Access Criteria
Survey data will be made available in csv format and will not require the use of specialized tools to be accessed or manipulated.

Locations