- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05380765
Developing a Positive Approach to Substance Use Prevention in North American Indian Adolescents
June 4, 2024 updated by: University of Rhode Island
The overall objective of this project is to develop and obtain preliminary data on acceptability, feasibility, and initial efficacy of Native PATHS.
This work is guided by the stage model guidelines for treatment development and adaptation 25.
Stage 1a will occur in two sequential steps.
First, the investigators will recruit youth who are in 5th - 8th grade and their family members (N=24, 12 youth, 12 adults 18+) to participate in three talking circle sessions to obtain feedback on the cultural adaptation and implementation of the treatment.
Next, the investigators will conduct an open label pilot (N=9).
Youth and their family members, (up to 3 per youth) will provide qualitative and quantitative feedback after each session.
In Stage 1b, 60 youth will participate in a pilot randomized controlled trial, testing the efficacy of the newly created program (n=30) against a wait list control (WLC) condition (n=30).
Ultimately, this program of research is expected to result in a well-specified, efficacious prevention program that could be readily disseminated and generalizable to other Indigenous populations with minimal adaptation.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
Alcohol is one of the primary determinants of health disparity among many Indigenous populations with rates of alcohol-attributable mortality substantially higher than for Whites (73.8 per 100,000 vs. 27.5),
and therefore, is a key threat to optimal health and well-being to Indigenous youth.
Indigenous youth living in both the US and Canada tend to begin using alcohol, tobacco, and other drugs (ATOD) at earlier ages than most other ethnic/racial groups, and tend to move more quickly to regular use, resulting in earlier onset of ATOD disorders.
Despite the severity of the problem, there continues to be an urgent unmet need for effective prevention programs that are culturally tailored to Indigenous populations of the US and Canada.
The overall objective of this project is to develop and obtain preliminary data on the acceptability, feasibility, and initial efficacy of Native PATHS (Positive Approaches to reducing Harm from Substance Use).
Native PATHS is a strengths-based, family prevention program for Indigenous youth in 5th-8th grade which focuses on delayed ATOD initiation.
The development of Native PATHS has been guided by formative work in this community, taking a behavioral economic and positive psychological approach to prevention.
Applied to prevention, behavioral economic theory focuses on reducing the availability of ATOD and increasing ATOD-free alternatives and the reinforcement received from engaging in ATOD-free activities.
Activities in Native PATHS will work with families to help with establishing ATOD-free rules, limit physical availability of ATOD in the home, and reinforce youths' participation in ATOD-free activities.
Positive psychological interventions (PPIs) focus on increasing positive emotions, life satisfaction, and well-being.
PPIs will be used to enhance the enjoyment received from ATOD-free activities and to improve life satisfaction.
Native PATHS is culturally consistent with North American Indigenous views of health that describe health in terms of a balance between the physical, spiritual, emotional, and mental aspects of life, which is represented in the teachings of the Medicine Wheel.
Collaboratively, the investigators will work together with tribal partners on further adaptation of the program to include family and Indigenous ways of parenting in a culturally meaningful way.
The overall goals proposed project will 1) finalize Native PATHS with participation from youth and family members in talking circles and an open pilot trial; 2) assess the effectiveness of Native PATHS in reducing ATOD initiation and intentions to use ATOD; 3) begin to evaluate the possible mechanisms/moderators of action including potential mediators future orientation and alternative reinforcer/activity engagement and reinforcement received, compared to a wait-list control group.
The investigators will also evaluate positive affect as a potential moderator of any treatment effect, such that those higher in positive affect will be less likely to engage in ATOD use and be less likely to endorse intentions to use ATOD.
Study Type
Interventional
Enrollment (Estimated)
60
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Nichea S Spillane, Ph.D.
- Phone Number: (401) 874-4252
- Email: nspillane@uri.edu
Study Locations
-
-
Rhode Island
-
Kingston, Rhode Island, United States, 02881-1967
- Recruiting
- University of Rhode Island
-
Contact:
- Nichea S Spillane, Ph.D.
- Phone Number: 401-874-4252
- Email: nspillane@uri.edu
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
10 years to 14 years (Child)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria - Youth Participants:
- residing in the First Nation community,
- identify as a member of a First Nation,
- be in grades 5th - 8th at time of enrollment, and
- one youth per household may participate.
Inclusion Criteria - Family Participants:
- at least 18 years of age
- reside within the First Nation community
- be identified, by the youth, as an important influence in their life
- be committed to helping the youth make good decisions regarding using substances
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Native PATHS Condition
A strengths-based, behavioral economic approach to increasing engagement and reinforcement for engaging in alternative activities.
|
A strengths-based, behavioral economic approach to increasing engagement and reinforcement for engaging in alternative activities.
|
|
No Intervention: Wait-List Control
Participants will receive the Native PATHS program once 6-month follow up surveys have been completed.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Past month alcohol use
Time Frame: Baseline
|
Respondents will be asked whether they have used alcohol in the past month (yes/no).
|
Baseline
|
|
Past month alcohol use
Time Frame: End of treatment (up to 12 weeks following baseline)
|
Respondents will be asked whether they have used alcohol in the past month (yes/no).
|
End of treatment (up to 12 weeks following baseline)
|
|
Past month alcohol use
Time Frame: Six months following end of treatment
|
Respondents will be asked whether they have used alcohol in the past month (yes/no).
|
Six months following end of treatment
|
|
Past three-month alcohol use
Time Frame: Baseline
|
Respondents will be asked whether they have used alcohol in the past three months (yes/no).
|
Baseline
|
|
Past three-month alcohol use
Time Frame: End of treatment (up to 12 weeks following baseline)
|
Respondents will be asked whether they have used alcohol in the past three months (yes/no).
|
End of treatment (up to 12 weeks following baseline)
|
|
Past three-month alcohol use
Time Frame: Six months following end of treatment
|
Respondents will be asked whether they have used alcohol in the past three months (yes/no).
|
Six months following end of treatment
|
|
Past month marijuana use
Time Frame: Baseline
|
Respondents will be asked whether they have used marijuana in the past month (yes/no).
|
Baseline
|
|
Past month marijuana use
Time Frame: End of treatment (up to 12 weeks following baseline)
|
Respondents will be asked whether they have used marijuana in the past month (yes/no).
|
End of treatment (up to 12 weeks following baseline)
|
|
Past month marijuana use
Time Frame: Six months following end of treatment
|
Respondents will be asked whether they have used marijuana in the past month (yes/no).
|
Six months following end of treatment
|
|
Past three-month marijuana use
Time Frame: Baseline
|
Respondents will be asked whether they have used marijuana in the past three months (yes/no).
|
Baseline
|
|
Past three-month marijuana use
Time Frame: End of treatment (up to 12 weeks following baseline)
|
Respondents will be asked whether they have used marijuana in the past three months (yes/no).
|
End of treatment (up to 12 weeks following baseline)
|
|
Past three-month marijuana use
Time Frame: Six months following end of treatment
|
Respondents will be asked whether they have used marijuana in the past three months (yes/no).
|
Six months following end of treatment
|
|
Past month cigarette smoking
Time Frame: Baseline
|
Respondents will be asked whether they have smoked cigarettes in the past month (yes/no).
|
Baseline
|
|
Past month cigarette smoking
Time Frame: End of treatment (up to 12 weeks following baseline)
|
Respondents will be asked whether they have smoked cigarettes in the past month (yes/no).
|
End of treatment (up to 12 weeks following baseline)
|
|
Past month cigarette smoking
Time Frame: Six months following end of treatment
|
Respondents will be asked whether they have smoked cigarettes in the past month (yes/no).
|
Six months following end of treatment
|
|
Past three-month cigarette smoking
Time Frame: Baseline
|
Respondents will be asked whether they have smoked cigarettes in the past three months (yes/no).
|
Baseline
|
|
Past three-month cigarette smoking
Time Frame: End of treatment (up to 12 weeks following baseline)
|
Respondents will be asked whether they have smoked cigarettes in the past three months (yes/no).
|
End of treatment (up to 12 weeks following baseline)
|
|
Past three-month cigarette smoking
Time Frame: Six months following end of treatment
|
Respondents will be asked whether they have smoked cigarettes in the past three months (yes/no).
|
Six months following end of treatment
|
|
Alcohol use intentions
Time Frame: Baseline
|
Respondent will be asked how often in the next month they think they will get drunk with friends and how often in the next month they would like to get drunk with friends, on a five-point scale from 0 (never) to 4 (10 or more times), where higher scores indicate more frequent intentions to use alcohol in the next month.
|
Baseline
|
|
Alcohol use intentions
Time Frame: End of treatment (up to 12 weeks following baseline)
|
Respondent will be asked how often in the next month they think they will get drunk with friends and how often in the next month they would like to get drunk with friends, on a five-point scale from 0 (never) to 4 (10 or more times), where higher scores indicate more frequent intentions to use alcohol in the next month.
|
End of treatment (up to 12 weeks following baseline)
|
|
Alcohol use intentions
Time Frame: Six months following end of treatment
|
Respondent will be asked how often in the next month they think they will get drunk with friends and how often in the next month they would like to get drunk with friends, on a five-point scale from 0 (never) to 4 (10 or more times), where higher scores indicate more frequent intentions to use alcohol in the next month.
|
Six months following end of treatment
|
|
Cigarette smoking susceptibility
Time Frame: Baseline
|
Cigarette smoking intentions will be measured using the Susceptibility to Smoking measure, which includes four items that asking respondents the likelihood that they will begin to smoke/experiment with cigarettes on a four-point scale from 0 (definitely not) to 3 (definitely yes), with higher scores indicating greater likelihood of intending to smoke cigarettes in the future.
|
Baseline
|
|
Cigarette smoking susceptibility
Time Frame: End of treatment (up to 12 weeks following baseline)
|
Cigarette smoking intentions will be measured using the Susceptibility to Smoking measure, which includes four items that asking respondents the likelihood that they will begin to smoke/experiment with cigarettes on a four-point scale from 0 (definitely not) to 3 (definitely yes), with higher scores indicating greater likelihood of intending to smoke cigarettes in the future.
|
End of treatment (up to 12 weeks following baseline)
|
|
Cigarette smoking susceptibility
Time Frame: Six months following end of treatment
|
Cigarette smoking intentions will be measured using the Susceptibility to Smoking measure, which includes four items that asking respondents the likelihood that they will begin to smoke/experiment with cigarettes on a four-point scale from 0 (definitely not) to 3 (definitely yes), with higher scores indicating greater likelihood of intending to smoke cigarettes in the future.
|
Six months following end of treatment
|
|
Marijuana use intentions
Time Frame: Baseline
|
Respondent will be asked how often in the next month they think they will use marijuana with friends and how often in the next month they would like to use marijuana with friends, on a five-point scale from 0 (never) to 4 (10 or more times), where higher scores indicate more frequent intentions to use marijuana in the next month.
|
Baseline
|
|
Marijuana use intentions
Time Frame: End of treatment (up to 12 weeks following baseline)
|
Respondent will be asked how often in the next month they think they will use marijuana with friends and how often in the next month they would like to use marijuana with friends, on a five-point scale from 0 (never) to 4 (10 or more times), where higher scores indicate more frequent intentions to use marijuana in the next month.
|
End of treatment (up to 12 weeks following baseline)
|
|
Marijuana use intentions
Time Frame: Six months following end of treatment
|
Respondent will be asked how often in the next month they think they will use marijuana with friends and how often in the next month they would like to use marijuana with friends, on a five-point scale from 0 (never) to 4 (10 or more times), where higher scores indicate more frequent intentions to use marijuana in the next month.
|
Six months following end of treatment
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Nichea S Spillane, Ph.D., University of Rhode Island
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
June 17, 2024
Primary Completion (Estimated)
May 31, 2025
Study Completion (Estimated)
May 31, 2025
Study Registration Dates
First Submitted
April 22, 2022
First Submitted That Met QC Criteria
May 13, 2022
First Posted (Actual)
May 19, 2022
Study Record Updates
Last Update Posted (Actual)
June 5, 2024
Last Update Submitted That Met QC Criteria
June 4, 2024
Last Verified
June 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- R34AA027619 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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