Engaging Family Members During Early SUD Treatment: A Hybrid Trial
ConditionSubstance Use Disorder (SUD)
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorStanford University
About this trial
The goal of this study is a fractional factorial optimization trial to optimize engagement in a CRAFT program for family members with loved ones in outpatient treatment for a substance use disorder.
This study aims to identify family engagement strategies that are feasible, acceptable, and appropriate and effective in increasing family member initiation with CRAFT. Participants will complete an iterative, online process where they will evaluate and rank different engagement strategies to identify the most optimal in increasing engagement and then participate in an optimization trial to identify which strategies were most effective in increasing family member engagement.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
18 years old or older
A parent, child, sibling, spouse/romantic partner, or other adult supporting a loved one who initiated SUD treatment in past 3 months
Cohabitating with their loved one
In frequent contact (in-person or virtual) with their loved one (at least 3x/week)
Disqualifiers
Does not have capacity to consent (e.g., severe cognitive impairment, in active psychosis, or developmental disabilities)
Does not understand English fluently
Trial design
Design model
Factorial
Treatments tested in this trial
Engagement Strategy 1
BehavioralEngagement Strategy
Engagement Strategy 2
BehavioralEngagement Strategy
Engagement Strategy 3
BehavioralEngagement Strategy
Engagement Strategy 4
BehavioralEngagement Strategy
Placebo
BehavioralNo engagement strategies
Treatment groups
100 Participants
are divided into 16 treatment groups16
Treatment groupsSee each treatment group below.
Group A: Aim 2: Arm 1Active comparator 4 interventions
Group B: Aim 2: Arm 2Active comparator 3 interventions
Group C: Aim 2: Arm 3Active comparator 2 interventions
Group D: Aim 2: Arm 4Active comparator 3 interventions
Group E: Aim 2: Arm 5Active comparator 2 interventions
Group F: Aim 2: Arm 6Active comparator 2 interventions
Group G: Aim 2: Arm 7Active comparator 2 interventions
Group H: Aim 2: Arm 8Active comparator 3 interventions
Group I: Aim 2: Arm 9Active comparator 2 interventions
Group J: Aim 2: Arm 10Active comparator 3 interventions
Group K: Aim 2: Arm 11Active comparator 1 intervention
Group L: Aim 2: Arm 12Active comparator 1 intervention
Group M: Aim 2: Arm 13Active comparator 1 intervention
Group N: Aim 2: Arm 14Active comparator 1 intervention
Group O: Aim 2: Arm 15Active comparator 2 interventions
Group P: Aim 2: Arm 16Placebo comparator 1 intervention
Trial outcomes
Primary outcomes
1
Attendance
Attend at least 1 eINSPIRE session
Time frame
2 months after baselineSecondary outcomes
1
Feasibility of Engagement Strategies
Assessed via the Intervention Usability Scale, score of 70+ indicates feasibility
Time frame
6 months from enrollment2
Acceptability of Engagement Strategies
Assessed via the Acceptability of Intervention Measure; 70%+ agree/strongly agree indicates acceptability
Time frame
6 months from enrollment3
Appropriateness of Engagement Strategies
Assessed via the Intervention Appropriateness Measure; 70%+ agree/strongly agree indicates appropriateness
Time frame
6 months from enrollmentSponsors and contacts
Click on the lead sponsor to view all of their trials.
Stanford University
Lead sponsor
National Institute on Drug Abuse (NIDA)
Collaborator
RAND
Collaborator
Northern California Institute of Research and Education
Collaborator
Family Health Centers of San Diego
Collaborator
Source ClinicalTrials.gov
This trial is not recruiting at the moment. You can still explore other options: