- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01821950
Evaluation of Yoga for Substance Use Risk Factors in a School Setting
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The long-term, programmatic goal of this research is to advance prevention of addictive behaviors especially substance use in normal adolescent psychological development. The overall goal of this proposal is to pilot test a novel, preventive intervention for adolescent substance use. More specifically, it will evaluate the efficacy of yoga taught during school to positively influence risk and protective factors of substance use and the initiation and severity of substance use.
This study involves a group randomized, controlled trial of yoga compared to physical education-as-usual for one school year, with a 6-month and 1-year follow-up, in order to accomplish the following specific aims:
Specific Aim 1 - To evaluate the efficacy of a school-based yoga program for reducing negative internalizing behaviors (negative mood, perceived stress, impulsivity) which are risk factors for adolescent substance use.
Specific Aim 2 - To evaluate the efficacy of this yoga program for promoting self-regulatory skills as protective factors against substance use in adolescence.
Specific Aim 3 - To conduct a preliminary evaluation of the efficacy of this yoga program for reducing substance use initiation and severity of use.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Massachusetts
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Boston, Massachusetts, United States, 02115
- Boston Latin School
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Registered for physical education class
Study Plan
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 |
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No Intervention: Physical education as usual
Physical education curriculum established by the school, including competitive sports, aerobic and anaerobic activities, balance and coordination skills.
Yoga is not a component of the curriculum.
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Experimental: Yoga during physical education
12 to 16 weeks of group yoga classes (approximately 32 classes per student), 30-45 minutes per class, 2-3 times per week, during physical education class.
Yoga program includes physical postures and movement, breathing exercises, partner/group games, deep relaxation and meditative techniques.
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12 to 16 weeks of group yoga classes (approximately 32 classes per student), 30-45 minutes per class, 2-3 times per week, during physical education class.
Yoga program includes physical postures and movement, breathing exercises, partner/group games, deep relaxation and meditative techniques.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Change in self-reported mood as measured by the 24-item Brunel University Mood Scale (BRUMS, total and 6 sub-scales)
Time Frame: Baseline; 1 week post-intervention; 6 months post-intervention; 1 year post-intervention
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The Brunel University Mood Scale (BRUMS) will be used to measure change in self-reported mood.
The BRUMS is designed specifically for assessing mood in adolescents.
It contains 24 adjectives that are all rated on a four-point scale to give a total mood score and scores for six subscales: tension, depression, anger, vigor, fatigue, and confusion.
In a validation sample of nearly 2,000 British adolescents (12 to 18 years of age), multi-sample confirmatory factor analysis showed high factor validity.
Criterion and construct validity were also acceptable.
Furthermore, BRUMS is sensitive to short-term changes.
More recently, the BRUMS has been successfully used in a large sample of American adolescents.
Negative affective states, such as mood, are clearly linked to substance use trajectories.
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Baseline; 1 week post-intervention; 6 months post-intervention; 1 year post-intervention
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Change in self-reported stress levels as measured by the 10-item Perceived Stress Scale (PSS)
Time Frame: Baseline; 1 week post-intervention; 6 months post-intervention; 1 year post-intervention
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The Perceived Stress Scale (PSS) is the most widely used psychological instrument for measuring the degree to which events are appraised as stressful during the last month.
Construct and convergent validity is adequate, since it is moderately correlated with other measures of stress and self-reported health status.
The 10 items in this scale were designed to tap how unpredictable, uncontrollable, and overloaded respondents find their lives.
The scale also includes a number of direct queries about current levels of experienced stress.
It is psychometrically sound based on epidemiological sampling that evaluated reliability and validity.
Furthermore, the PSS has been administered to mid-adolescents (8th and 9th graders) with good internal consistency.
Psychological stress has been associated with substance use in studies of adolescents and college students.
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Baseline; 1 week post-intervention; 6 months post-intervention; 1 year post-intervention
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Change in self-reported impulsive behavior as measured by the 59-item Urgency, Premeditation, Perseverance, and Sensation Seeking Plus (UPPS-P) Impulsive Behavior scale (4 sub-scales)
Time Frame: Baseline; 1 week post-intervention; 6 months post-intervention; 1 year post-intervention
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The Urgency, Premeditation, Perseverance, and Sensation Seeking Plus (UPPS-P) Impulsive Behavior scale is a 59-item self-report scale developed by Whiteside and Lynam to measure the multi-dimensional nature of impulsivity.
Items are scored based on a four-point Likert-type scale as follows: 1) agree strongly, 2) agree somewhat, 3) disagree somewhat, and 4) disagree strongly.
Factor analysis of eight other established scales that address impulsivity (in whole or part) revealed four factors that became the subscales in the UPPS-P: (lack of) Premeditation (11 items), Negative Urgency (11 items), Positive Urgency (14 items), Sensation Seeking (12 items), and (lack of) Perseverance (10 items).
Internal consistency for these subscales showed alpha coefficients that ranged from 0.82 to 0.91.
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Baseline; 1 week post-intervention; 6 months post-intervention; 1 year post-intervention
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Change in self-reported soothability, planfulness, and distractibility as measured by the Kendall-Wilcox Self-Control Schedule (3 sub-scales).
Time Frame: Baseline; 1 week post-intervention; 6 months post-intervention; 1 year post-intervention
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Soothability.
The Soothability scale of the Kendall-Wilcox Self-Control Schedule assesses adolescents' capabilities to reduce emotional tension and control calmness when distressed.
This 5-item scale includes items such as, "If I get annoyed about something, I can get over it pretty quick," and "I can easily calm down when I am excited or "wound up".
Planfulness.
This 7-item scale derived from the Kendall-Wilcox Self-Control Schedule assesses individuals' planfulness in everyday situations.
Sample items include "I like to plan things way ahead of time."
Distractibility.
Adolescent tendency to be distracted from daily work is measured by a 6-item scale derived from the Kendall-Wilcox Self-Control Schedule.
Sample items include "I like to switch from one thing to another."
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Baseline; 1 week post-intervention; 6 months post-intervention; 1 year post-intervention
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Change in self-reported anger control and anger rumination as measured by the Children's Anger Management Scale (2 sub-scales)
Time Frame: Baseline; 1 week post-intervention; 6 months post-intervention; 1 year post-intervention
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Anger Control.
Adolescents' anger management is assessed by the Anger Control subscale (4 items) of Children's Anger Management Scale (CAMS).
Sample items include, "I can stop myself from losing my temper."
Anger Rumination.
The Anger Rumination subscale of the CAMS is used to measure an anger management domain of emotional SR.
Items include, "I get angry thinking about things that happened in the past."
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Baseline; 1 week post-intervention; 6 months post-intervention; 1 year post-intervention
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Change in self-reported sadness control and sadness rumination as measured by the Children's Sadness Management Scale (CSMS) (2 sub-scales)
Time Frame: Baseline; 1 week post-intervention; 6 months post-intervention; 1 year post-intervention
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Sadness Control.
A 5-item subscale of the Children's Sadness Management Scale (CSMS) measures what adolescents might or might not do when they are feeling sad or down.
The Sadness Control subscale includes items such as, "When I'm feeling down, I can control my sadness and carry on with things."
Sadness Rumination.
This 3-item measure for Sadness Rumination adapted from the CSMS assesses adolescents' emotional capabilities in dealing with sadness.
Items include, "When people do something to make me sad, I don't forget about it."
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Baseline; 1 week post-intervention; 6 months post-intervention; 1 year post-intervention
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Change in self-reported affective lability as measured by the Affective Lability Scale (originally 54 items, adapted to 10 items)
Time Frame: Baseline; 1 week post-intervention; 6 months post-intervention; 1 year post-intervention
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Affective Lability.
A 10-item scale is adapted from the 54-item Affective Lability Scale.
The Affective lability scale measures adolescents' tendency to change mood frequently.
Sample items include, "My moods change a lot from day to day," and "I often switch back and forth from feeling irritated to feeling comfortable and relaxed."
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Baseline; 1 week post-intervention; 6 months post-intervention; 1 year post-intervention
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Change in self-reported anger coping, problem solving, situation redefinition, impatience, and self-criticism as measured by the Wills Coping Inventory (5 sub-scales)
Time Frame: Baseline; 1 week post-intervention; 6 months post-intervention; 1 year post-intervention
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The following subscales from the Wills Coping Inventory will be used: Anger coping, problem solving, situation redefinition, impatience, self-criticism.
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Baseline; 1 week post-intervention; 6 months post-intervention; 1 year post-intervention
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Change in self-reported positive self-reinforcement as measured by the 8-item Heiby Self-Reinforcement Inventory
Time Frame: Baseline; 1 week post-intervention; 6 months post-intervention; 1 year post-intervention
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Positive Self-Reinforcement.
An 8-item scale is adapted from the Heiby Self-Reinforcement Inventory to measure adolescents' self-"reward" to prompt themselves to continue to perform a desired behavior.
Items include "when I do something right, I take time to enjoy the feeling"
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Baseline; 1 week post-intervention; 6 months post-intervention; 1 year post-intervention
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Change in self-reported present and future time perspective as measured by the Zimbardo Time Perspective Inventory (2 sub-scales)
Time Frame: Baseline; 1 week post-intervention; 6 months post-intervention; 1 year post-intervention
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Future Time Perspective.
An orientation toward present occurrences (e.g., seek out activities that produce immediate satisfaction such as alcohol use) versus future occurrences (e.g., invest in activities that require more effort but have positive long-term consequences such as physical exercise) has been considered to have significant effects on adolescent substance abuse: future orientation to have preventive effects and present orientation to have harmful effects on adolescent substance abuse and risky behaviors.
This 7-item scale on Future Time Perspective is adapted from the Zimbardo Time Perspective Inventory (ZTPI).
Items include "I am able to resist temptation when I know there is work to be done".
Present Time Perspective.
A 7-item scale on Present Time Perspective is derived from the ZTPI.
Sample items include, "I think it's useless to plan too far ahead, because things hardly ever turn out the way I planned."
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Baseline; 1 week post-intervention; 6 months post-intervention; 1 year post-intervention
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Change in self-reported impulsiveness as measured by the Eysenck Impulsiveness Questionnaire (EIQ) (1 subscale)
Time Frame: Baseline; 1 week post-intervention; 6 months post-intervention; 1 year post-intervention
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Impulsiveness.
A 7-item scale from the Eysenck Impulsiveness Questionnaire (EIQ) assesses tendency for adolescents' impulsive responding.
Sample items include "I often do things without stopping to think," and "I often get into trouble because I do things without thinking."
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Baseline; 1 week post-intervention; 6 months post-intervention; 1 year post-intervention
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Change in self-reported substance use as measured by the Youth Risk Behavior Survey (YRBS) (4 subscales)
Time Frame: Baseline; 1 week post-intervention; 6 months post-intervention; 1 year post-intervention
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Youth Risk Behavior Survey (YRBS) Middle School Version (http://www.cdc.gov/HealthyYouth/yrbs/index.htm).
This is a nationally validated scale that measures substance use in children and adolescents.
There are 16 questions in the substance use category of the 2013 middle school version of the YRBS for use of tobacco (8 questions), alcohol (2 questions), marijuana (2 questions), and other drugs (4 questions), taking approximately 10 minutes to complete.
Each question includes an answer that allows participants to indicate whether they have ever used the substance, which will serve as a measure of use initiation over the time course of the entire study.
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Baseline; 1 week post-intervention; 6 months post-intervention; 1 year post-intervention
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Change in self-reported substance use willingness as measured by the 13-item Substance Use Willingness Questionnaire
Time Frame: Baseline; 1 week post-intervention; 6 months post-intervention; 1 year post-intervention
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Substance Use Willingness Questionnaire.
The Substance Use Willingness Questionnaire is composed of 13 items that ask how willing the participant would be to try cigarettes (3 questions), alcohol (3 questions), marijuana (3 questions), and other drugs (4 questions).
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Baseline; 1 week post-intervention; 6 months post-intervention; 1 year post-intervention
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Collaborators and Investigators
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
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
- 2007P002600B
- R34DA032756 (U.S. NIH Grant/Contract)
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