- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04478240
Automating Peer Learning to Reduce Alcohol Use and Related Deviant Behavior in Secondary School (PeerLearning)
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Schools (N = 12) will be randomly assigned to intervention or waitlist control conditions, and data will be collected immediately in the fall (i.e., baseline measure) and in the spring, approximately 6 months later (i.e., post-treatment assessment). Overall, the investigators will have two assessment points. Data will be collected from teachers and students via on-line surveys (i.e., Qualtrics) and through observations; see below on the Measures. Intervention schools will receive training and access to the PeerLearning.net app immediately, whereas control schools will receive access in the spring after the second wave of data collection is completed.
The investigators hypothesize that usage of PeerLearning.net will promote increasing levels of prosocial behavior and have a significant suppressive effects on alcohol use and related outcomes (i.e., tobacco/marijuana use, antisocial behavior, bullying/victimization, mental health problems) and salutary effects on social-emotional skills, peer relations, and sleep quality. The investigators hypothesize that there will be effects of dosage (i.e., usage of the app). Finally, the investigators will examine differences in program effects by sex (gender) and ethnicity, which the investigators expect to be small or nonexistent.
Participants will include both teachers and students at 12 middle and high schools, cluster randomized to intervention vs. waitlist control. Teachers will use PeerLearning.net to design and deliver small-group peer learning lessons during the school year. The investigators will not exclude any participant based upon race/ethnicity, gender, or disability. Participating schools, teachers, and students will be rewarded.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Oregon
-
Eugene, Oregon, United States, 97403
- Oregon Research Behavioral Intervention Strategies, Inc.
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- All teachers and students in participating schools will be eligible to participate.
Exclusion Criteria:
- The investigators will not exclude any participant based upon race/ethnicity, gender, or disability.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention (access to PeerLearning.net)
Teachers and students in intervention schools will be given access to PeerLearning.net
software for the purposes of instruction for the 2021-2022 school year.
|
PeerLearning.net is a software package that supports teachers in designing and delivering peer learning lessons, either in-person or remotely while students are learning at home. Peer learning is an instructional technique that puts students in groups under conditions of positive interdependence, where they are incentivized to work together and promote the success of one another. Peer Learning lessons also ensure individual accountability and explicitly observe for and reward specific group social skills (e.g., encouraging participation, checking for understanding). Peer Learning also includes group processing after the lesson is completed so that the students in the groups have an opportunity to discuss what they did well and what could use improvement; they also have the opportunity to provide positive reinforcement to one another for contributing to the success of the group. |
|
No Intervention: Passive Control (no intervention)
Teachers and students in control schools will conduct instruction as usual without PeerLearning.net.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Alcohol and other drug (AOD) use
Time Frame: Pre and 6 months post-treatment
|
Youth will complete the SAMHSA Participant Outcome Measures for Discretionary Programs.
This survey tool was used as part of SAMHSA's national cross-site evaluation and is comprised of questions that include alcohol, tobacco, and other drug (ATOD) use and knowledge; ATOD beliefs and perceived risk of harm from ATOD use; and future intentions to use drugs.
The investigators will also assess binge alcohol use (i.e., occasions at which 5/more drinks were consumed).
The minimum score is zero.
|
Pre and 6 months post-treatment
|
|
Antisocial/prosocial behavior and mental health
Time Frame: Pre and 6 months post-treatment
|
The Strengths and Difficulties Questionnaire (SDQ),has subscales for Conduct Problems (antisocial behavior), Prosocial Behavior, and Emotional Problems.
Subscales for conduct problems (e.g., "I get very angry and often lose my temper"), emotional problems (e.g., "I worry a lot"), and prosocial behavior (e.g., "I usually share with others") items scores 1 (none) to 3 (a lot), and the investigators average these, so the minimum is 1 and the maximum is 3.
|
Pre and 6 months post-treatment
|
|
Bullying and victimization
Time Frame: Pre and 6 months post-treatment
|
The Illinois Aggression Scales (Espelage & Holt, 2001) includes three subscales.
The bullying and victimization subscales will be used.
The 9-item Illinois Bully Scale measures frequency of teasing, name-calling, and social exclusion within the last 30 days.
The 4-item Illinois Peer Victimization Scale assesses verbal and physical peer victimization within the past 30 days.
Each item scores between 0 (none) and 4 (a lot), and the investigators average these so the minimum score is zero and the maximum is 4.
|
Pre and 6 months post-treatment
|
|
Sleep quality
Time Frame: Pre and 6 months post-treatment
|
Pittsburgh Sleep Quality Inventory (PSQI) contains a series of items for sleep duration, sleep onset latency, and perceived sleep quality.
Higher scores indicate greater duration, latency, and quality.
|
Pre and 6 months post-treatment
|
|
Stress
Time Frame: Pre and 6 months post-treatment
|
Perceived Stress Scale (PSS); items are scored from 1 to 4 and averaged.
Higher scores indicate more stress.
|
Pre and 6 months post-treatment
|
|
Peer support
Time Frame: Pre and 6 months post-treatment
|
Classroom Life Scale; items are scored from 1 to 5 and averaged.
Higher scores indicate more peer support.
|
Pre and 6 months post-treatment
|
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Peer relations
Time Frame: Pre and 6 months post-treatment
|
Peer Relatedness Scale items are scored from 1 to 4 and averaged.
Higher scores indicate more positive peer relations.
|
Pre and 6 months post-treatment
|
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Social-emotional skills
Time Frame: Pre and 6 months post-treatment
|
Social and Emotional Competency Long-Form Assessment contains five subscales corresponding to the 5 dimensions of Social-Emotional Learning (Self-Awareness: a person's ability to recognize their emotions, thoughts, and values; Self-Management: a person's ability to regulate their emotions, thoughts, and behaviors; Social Awareness: the ability to recognize and empathize with others' perspectives and understand social norms; Relationship Skills: the ability to communicate and cooperate effectively, and to seek and offer help when needed; and Responsible Decision-Making: the ability to make constructive personal choices in relation to social norms and personal safety).
Items are scored from 1 to 4 and averaged, with higher scores indicating greater social-emotional skill.
|
Pre and 6 months post-treatment
|
Collaborators and Investigators
Publications and helpful links
General Publications
- Espelage DL, Holt MK. Bullying and Victimization During Early Adolescence, Journal of Emotional Abuse. 2001. 2:2-3, 123-142, DOI: 10.1300/J135v02n02_08
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- AA027422
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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