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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02339363
Other study ID # Quach-1-2013
Secondary ID
Status Completed
Phase Phase 1/Phase 2
First received January 9, 2015
Last updated January 14, 2015
Start date March 2013
Est. completion date July 2013

Study information

Verified date January 2015
Source Alliant International University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The present study was a randomized controlled trial that explored the feasibility, acceptability, and effectiveness of short-term mindfulness training among adolescents. The primary purpose was to investigate the effectiveness of two main Mindfulness-Based Stress Reduction components—sitting meditation and hatha yoga—on working memory, stress, anxiety and mindfulness. The influence of daily home practice compliance on intervention outcomes was also examined.


Description:

The present study was a randomized controlled trial that explored the feasibility, acceptability, and effectiveness of short-term mindfulness training among adolescents. The primary purpose was to investigate the effectiveness of two main Mindfulness-Based Stress Reduction components—sitting meditation and hatha yoga—on working memory, stress, anxiety and mindfulness. The influence of daily home practice compliance on intervention outcomes was also examined. Participants (N = 198 adolescents) were recruited from a large public middle school in southern California. Participants were randomly assigned to sitting meditation, hatha yoga, or a waitlist control group. Participants were asked to complete a computerized working memory task, and self-report measures of perceived stress, anxiety, and mindfulness at pre- and post-intervention/waitlist, as well as one-month follow-up. A series of mixed-design analyses of variance (ANOVAs) were used to examine changes in working memory, stress, anxiety, and mindfulness between groups at pre- and post- intervention.


Recruitment information / eligibility

Status Completed
Enrollment 198
Est. completion date July 2013
Est. primary completion date June 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 12 Years to 17 Years
Eligibility Inclusion Criteria:

- Students currently enrolled in school

- Between the ages of 12 - 17 years old

- English speaking—to understand and complete the measures

- Able to attend the weekly hatha yoga or sitting meditation sessions

- Not reporting any injuries or health condition(s) that might limit their physical activity

Exclusion Criteria:

- hearing impairments, injuries, or physical disabilities that would hinder them from fully participating in intervention

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Factorial Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
Sitting Meditation
4 weeks Sitting Meditation
Hatha yoga
4 weeks of Hatha yoga

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Alliant International University

Outcome

Type Measure Description Time frame Safety issue
Primary Working Memory Capacity: Automated Operational Span Task (AOSPAN) Participants completed the AOSPAN prior to beginning their group condition (sitting meditation, Hatha yoga, or waitlist control) and again at the end of the 4-week intervention (waitlist) period. pre-intervention and post-intervention (waitlist), t the end of the 4-week intervention (waitlist) period No
Secondary Stress: Perceived Stress Scale (PSS-10) Participants completed the PSS-10 prior to beginning their group condition (sitting meditation, Hatha yoga, or waitlist control) and again at the end of the 4-week intervention (waitlist) period. pre-intervention and post-intervention (waitlist), t the end of the 4-week intervention (waitlist) period No
Secondary Anxiety: Screen for Child Anxiety and Related Emotional Disorders (SCARED) Participants completed the SCARED prior to beginning their group condition (sitting meditation, Hatha yoga, or waitlist control) and again at the end of the 4-week intervention (waitlist) period. pre-intervention and post-intervention, t the end of the 4-week intervention (waitlist) period No
Secondary Mindfulness: Child Acceptance and Mindfulness Measure (CAMM) Participants completed the CAMM prior to beginning their group condition (sitting meditation, Hatha yoga, or waitlist control) and again at the end of the 4-week intervention (waitlist) period. pre-intervention and post-intervention (waitlist), t the end of the 4-week intervention (waitlist) period No
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