- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT02140359
Enhancing Housing First Programs With a Social Network Substance Use Intervention
21 novembre 2017 mis à jour par: David Kennedy, RAND
Housing First programs are promising approaches to transitioning substance using chronically homeless adults to affordable housing.
However, Housing First programs need to provide support to residents to adjust to their changing social environments.
The proposed project fulfills a critical gap by developing an electronic tool for a social network intervention using motivational interviewing techniques as well as results of a pilot test of the tool.
The hypothesis to be tested is that Housing First residents who are given the intervention will be significantly more motivated to change their drinking, drug use, sexual risk behaviors, and social networks compared to controls receiving usual care.
Aperçu de l'étude
Statut
Complété
Les conditions
Intervention / Traitement
Description détaillée
We propose a 3-year study to develop and pilot test a social network substance use and HIV-risk intervention for permanent supportive housing program residents in the Skid Row area of Los Angeles.
The intervention will be developed for residents at the Skid Row Housing Trust (SRHT), one of the largest Housing First providers in Los Angeles.
Housing First residents are not required to abstain from alcohol and drugs as a requirement of their residency.
There is some evidence that providing housing rapidly to chronically homeless persons--along with support--helps to reduce substance use and HIV risk behaviors in the short term because homelessness is the primary cause of high-risk behavior.
However, the evidence thus far is limited.
One aspect that has not received much research attention is the needs of Housing First residents for support to transition their social networks while transitioning out of homeless into residency in a Housing First program.
New residents are exposed to a wide range of potentially negative social influences while also having greater potential to reconnect with lost positive ties.
This project will develop a social network intervention to residents of SRHT in order to increase their knowledge about their social networks and enhance their motivation to make necessary changes to improve their ability to reduce or continue to abstain from high-risk behavior.
The intervention sessions will enhance the weekly support meetings that SRHT case workers already conduct with new residents during their first 6 months of residency.
Case workers will be trained to deliver the 30-minute intervention sessions using a motivational interviewing style.
The intervention will be developed so that case managers can deliver it with the aid of an electronic tablet device.
The tablet will guide them in collecting information about the residents' social networks and then display several diagrams highlighting various aspects of the residents' networks.
They will then use motivational interviewing techniques to guide residents to think about how their network currently functions, how they would like it to function, and what steps they can take to make changes necessary to achieve goals related to reducing their substance use and sexual risk behaviors.
The intervention will be delivered by case managers across four sessions (at baseline and at two-week intervals).
We anticipate that residents who participate in this intervention will develop new strategies in their interactions with their social networks that will facilitate a reduction in their high-risk behavior.
Type d'étude
Interventionnel
Inscription (Réel)
50
Phase
- N'est pas applicable
Contacts et emplacements
Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.
Lieux d'étude
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California
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Los Angeles, California, États-Unis, 90021
- Skid Row Housing Trust
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Santa Monica, California, États-Unis, 90407
- RAND Corporation
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Critères de participation
Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.
Critère d'éligibilité
Âges éligibles pour étudier
18 ans et plus (Adulte, Adulte plus âgé)
Accepte les volontaires sains
Oui
Sexes éligibles pour l'étude
Tout
La description
Inclusion Criteria:
- New residents of Skid Row Housing Trust receiving permanent supportive housing
Exclusion Criteria:
- Age younger than 18
- Does not speak English
- Cognitively impaired either by identifying those having a diagnosis of dementia in the new resident intake interview or using the Short Blessed Scale Exam)
- Does not screen positive for past -year harmful AOD use using the AUDIT-C (a score > 4 for men and > 3 for women) and DAST (a score greater than 2).
Plan d'étude
Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Soins de soutien
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
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Aucune intervention: Control Group: Usual Care
Residents of a housing first permanent supporting housing program will be randomly assigned to this arm after screening and baseline assessments.
They will meet with case managers according to the usual procedures for new residents and will be given a standard case manager interaction.
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Expérimental: Motivational Network Interview Recipients
Residents of a housing first permanent supporting housing program will be randomly assigned to this arm after screening and baseline assessments.
They will meet roughly every two weeks with a case manager and answer questions about their social network, will be shown visual feedback about their networks, and will participate in a motivational interview conducted by the case managers.
The questions and visualizations will be facilitated by an electronic tool for presenting screens with questions, capturing responses, processing and visualizing social network data.
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Residents of a housing first permanent supporting housing program will be randomly assigned to this arm after screening and baseline assessments.
They will meet roughly every two weeks with a case manager and answer questions about their social network, will be shown visual feedback about their networks, and will participate in a motivational interview conducted by the case managers.
The questions and visualizations will be facilitated by an electronic tool for presenting screens with questions, capturing responses, processing and visualizing social network data.
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Readiness to change alcohol and other drug use
Délai: Baseline and 13-14 weeks (post intervention)
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Measured with 12 item Readiness to Change Questionnaire (RTCQ) and a one item Contemplation Ladder
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Baseline and 13-14 weeks (post intervention)
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Readiness to change risky sexual behavior
Délai: Baseline and 13-14 weeks (post intervention)
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11 item Readiness to Change Risky Sexual Behavior (RTCQ-SB) scale a one item Contemplation Ladder
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Baseline and 13-14 weeks (post intervention)
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Self efficacy to change alcohol and other drug use
Délai: Baseline and 13-14 weeks (post intervention)
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Measured with two questionnaire items that assess the participant's importance and self-efficacy to stop alcohol and other drug use and 4 items from the Alcohol Abstinence Self-Efficacy Scale (AASE) which measure how confident participants feel in their ability to abstain from alcohol use when depressed, relaxed, craving substances, and offered alcohol.
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Baseline and 13-14 weeks (post intervention)
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Self efficacy to change risky sexual behavior
Délai: Baseline and 13-14 weeks (post intervention)
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Measured with 4 item Self-Efficacy to Use Condoms scale
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Baseline and 13-14 weeks (post intervention)
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Self-efficacy to change social networks
Délai: Baseline and 13-14 weeks (post intervention)
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Two item ladder scale item measuring importance and self-efficacy to change social networks.
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Baseline and 13-14 weeks (post intervention)
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Perceived Social Network support and approval/disapproval of alcohol, drug use, and risky sex.
Délai: Baseline and 13-14 weeks (after intervention)
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Measures of Perceived Social Support and ratings of network members on emotional closeness, drinking, drug use, safe-sex behavior, and approval/disapproval of high-risk behavior of social network members based on the Important People Drug and Alcohol Interview.
Raw network data to provide measures will result from a personal network interview in which participants will name 20 network member and answer questions about each of them and their relationships with each other.
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Baseline and 13-14 weeks (after intervention)
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Drug and Alcohol use
Délai: Baseline and 13-14 weeks (after intervention is completed)
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Assessed with a Timeline Followback calendar structured interview that measures alcohol and drug use through recall aided by a calendar.
Participants will be asked quantity and intensity of drinking and drug use to calculate a quantity-frequency index for both drinking and drug use.
Self-reports of non-use will be validated with a Oral Fluid Test.
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Baseline and 13-14 weeks (after intervention is completed)
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HIV risk behavior
Délai: baseline and 13-14 weeks (after intervention completion)
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Survey items asking if the participant engaged in unprotected sex and concurrent sexual relationships overall and with particular partners in the past 90 days.
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baseline and 13-14 weeks (after intervention completion)
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Change in social network composition and structure
Délai: baseline and 13-14 weeks (after intervention completion)
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Measures of network composition and structure will be constructed from raw network data.
Raw network data result from a personal network interview in which participants will name 20 network member and answer questions about each of them and their relationships with each other.
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baseline and 13-14 weeks (after intervention completion)
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Autres mesures de résultats
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Satisfaction with Intervention
Délai: 13-14 weeks (after intervention)
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Administration of the Client Satisfaction Questionnaire (CSQ-8), an 8-item Likert-type measure of client feedback regarding services provided in a treatment program.
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13-14 weeks (after intervention)
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Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Parrainer
Les enquêteurs
- Chercheur principal: David P Kennedy, PhD, RAND
Publications et liens utiles
La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.
Publications générales
- Kennedy DP, Osilla KC, Hunter SB, Golinelli D, Maksabedian Hernandez E, Tucker JS. Restructuring personal networks with a Motivational Interviewing social network intervention to assist the transition out of homelessness: A randomized control pilot study. PLoS One. 2022 Jan 21;17(1):e0262210. doi: 10.1371/journal.pone.0262210. eCollection 2022.
- Osilla KC, Kennedy DP, Hunter SB, Maksabedian E. Feasibility of a computer-assisted social network motivational interviewing intervention for substance use and HIV risk behaviors for housing first residents. Addict Sci Clin Pract. 2016 Sep 7;11(1):14. doi: 10.1186/s13722-016-0061-x.
- Kennedy DP, Hunter SB, Chan Osilla K, Maksabedian E, Golinelli D, Tucker JS. A computer-assisted motivational social network intervention to reduce alcohol, drug and HIV risk behaviors among Housing First residents. Addict Sci Clin Pract. 2016 Mar 15;11(1):4. doi: 10.1186/s13722-016-0052-y.
Dates d'enregistrement des études
Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.
Dates principales de l'étude
Début de l'étude
1 juin 2015
Achèvement primaire (Réel)
1 octobre 2016
Achèvement de l'étude (Réel)
1 juillet 2017
Dates d'inscription aux études
Première soumission
14 mai 2014
Première soumission répondant aux critères de contrôle qualité
15 mai 2014
Première publication (Estimation)
16 mai 2014
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
24 novembre 2017
Dernière mise à jour soumise répondant aux critères de contrôle qualité
21 novembre 2017
Dernière vérification
1 novembre 2017
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- R34DA034855 (Subvention/contrat des NIH des États-Unis)
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .