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临床试验/NCT07098845
NCT07098845进行中(未招募)不适用

Testing a Mindfulness-Based Intervention With a Multi-Modal Adaptive Supplement for Stress-Related Problems in College Students

Colorado State University8 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2025年9月1日最近更新:
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
120
试验地点
8
主要终点
Program-specific intervention knowledge evaluations

研究概览

简要总结

The investigators hope to add to the feasible, acceptable, and effective interventions that offer reductions in depression, anxiety, and stress for students at U.S. colleges and universities, the majority of whom experience mental health problems but the minority of whom who receive adequate mental health support. By studying the extent to which a multi-modal supplement boosts effects for a mindfulness-based intervention (and comparing both to an active health education control program) to reduce depression, anxiety, and stress, the proposed research seeks to rigorously investigate complementary and integrative health interventions and their roles in improving health.

详细描述

There have been dramatic and concerning increases in rates of psychological distress in students enrolled in US colleges and universities over the last decade. The majority of college students in the last year experienced mental health problems, and if left untreated, symptoms of these problems have serious individual and public health consequences, both in the short- and long-term. However the vast majority of students do not receive professional mental health support because traditional treatments are perceived as ineffective and inconvenient. Additionally, many on campus resources cannot meet the demand of students needing support. As a result, it is critical to identify acceptable and effective interventions to address what is being called a "campus mental health crisis." Mindfulness-based interventions (MBIs) are very well-liked by college students, most of whom are late adolescents; in addition they are effective at increasing mindfulness and emotion regulation as well as reducing stress and depression. However, MBI effects have typically been small-to-moderate. Outside of the mindfulness literature, technological supplements to group-based programs like MBIs have been found to be effective at increasing intervention efficacy. The investigative team developed the first multi-modal adaptive supplement to an MBI (5K01AT009592), Learning To BREATHE PLUS ( L2B PLUS), which supplements an evidence-based group MBI with multiple methods of support for practicing mindfulness in daily life. The investigators program of research provides evidence at a single site that L2P PLUS is feasible and highly acceptable to adolescents, results in sustained levels of engagement across the group program period, and appears to be more effective than the standard Learning To BREATHE group program (L2B) at increasing daily mindfulness practice and consistency of mindfulness during stress as well as reducing psychological distress. In turn, L2B appears more effective in reducing stress-related behavior compared to an active, didactic health education control (HealthEd). Building directly on the investigators' prior work the proposed R01 study is a multisite, pilot randomized controlled trial implemented at four sites in order to prepare for a future multi-site efficacy trial testing the effects of L2B PLUS relative to the standard L2B program and HealthEd on depression, anxiety, and stress. Specific aims of the current proposal are to: 1) evaluate multi-site fidelity of training and implementation of 6-week L2B PLUS, 6 week L2B and 6-week HealthEd to college students experiencing stress, 2) test multi-site feasibility and acceptability of recruitment, retention, and protocol adherence for randomized control trial (RCT) involving L2B PLUS, L2B, and HealthEd, and 3) modify training/implementation and protocol for a future, fully powered multi-site efficacy trial. Completion of these aims will prepare us for an adequately-powered, multi-site efficacy trial, and ultimately inform a complementary and integrative approach to supporting college students experiencing problems with stress.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Double (Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 25 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • aged 18-25 years
  • enrolled in a college or university
  • experiencing elevated stress
  • plan to be available in-person in the semester following the study
  • own a smart phone.

排除标准

  • have several depressive symptoms
  • have suicidal ideation.

研究组 & 干预措施

HealthEd

Active Comparator

干预措施: HealthEd (Behavioral)

Learning to BREATHE (L2B)

Active Comparator

干预措施: Learning to BREATHE (Behavioral)

Learning to BREATHE Plus (L2B PLUS)

Experimental

干预措施: Learning to BREATHE Plus (Behavioral)

结局指标

主要结局

Program-specific intervention knowledge evaluations

时间窗: 2 months before baseline

Post-training L2B, L2B PLUS, and HealthEd knowledge assessments (0-25) will be completed by facilitators with higher scores indicating higher intervention knowledge

Number of eligible participants recruited with elevated stress as assessed by the Perceived Stress Scale

时间窗: Within a 12-month period

Study goal of 120 participants total across 4 sites who have elevated stress (\>14) on the Perceived Stress Scale (0-40) where higher scores indicate higher stress

Program-specific facilitator adherence ratings of mock intervention group sessions

时间窗: 2 months before baseline

Facilitator adherence to each intervention manual (0-100) for L2B, L2B PLUS, and HealthEd, during mock sessions after intervention facilitation training where higher scores mean higher adherence

Acceptability ratings of intervention by participants

时间窗: Within one-month of intervention end

Acceptability ratings (1-5) with higher scores meaning higher acceptability

Qualitative assessment of acceptability of interventions

时间窗: Within one-month of intervention end

Focus within group programs will qualitatively assess the acceptability of interventions

Percent of participants retained at post-test

时间窗: Post intervention, 6 weeks after baseline

Percent retention at six-month follow-up

时间窗: 32 weeks after baseline

Program-specific facilitator competence ratings of mock intervention group sessions

时间窗: 2 months before baseline

Facilitator competence of each intervention manual (0-100) for L2B, L2B PLUS, and HealthEd, during mock sessions after intervention facilitation training where higher scores mean higher competence

Percentage of eligible students who enroll

时间窗: Within a 12-month period

Percentage of enrolled participants who attend 5/6 intervention sessions

时间窗: During 6-week interventions

Adherence to standardized data collection protocol measured via standardized checklists

时间窗: At baseline, 6 weeks after, and 32 weeks after

Percentage of data collection protocol adhered to by assessors (0-100) with higher scores indicating better adherence

Qualitative assessment of acceptability of interventions

时间窗: Within one-month of intervention end

Focus within group programs will qualitatively assess the acceptability of interventions

Percent of participants retained at post-test

时间窗: Post intervention, 6 weeks after baseline

Percent retention at six-month follow-up

时间窗: 32 weeks after baseline

Adherence to standardized data collection protocol measured via standardized checklists

时间窗: At baseline, 6 weeks after, and 32 weeks after

Percentage of data collection protocol adhered to by assessors (0-100) with higher scores indicating better adherence

Acceptability ratings of intervention by participants

时间窗: Within one-month of intervention end

Acceptability ratings (1-5) with higher scores meaning higher acceptability

Program-specific intervention knowledge evaluations

时间窗: 2 months before baseline

Post-training L2B, L2B PLUS, and HealthEd knowledge assessments (0-25) will be completed by facilitators with higher scores indicating higher intervention knowledge

Number of eligible participants recruited with elevated stress as assessed by the Perceived Stress Scale

时间窗: Within a 12-month period

Study goal of 120 participants total across 4 sites who have elevated stress (\>14) on the Perceived Stress Scale (0-40) where higher scores indicate higher stress

Program-specific facilitator adherence ratings of mock intervention group sessions

时间窗: 2 months before baseline

Facilitator adherence to each intervention manual (0-100) for L2B, L2B PLUS, and HealthEd, during mock sessions after intervention facilitation training where higher scores mean higher adherence

Program-specific facilitator competence ratings of mock intervention group sessions

时间窗: 2 months before baseline

Facilitator competence of each intervention manual (0-100) for L2B, L2B PLUS, and HealthEd, during mock sessions after intervention facilitation training where higher scores mean higher competence

Percentage of eligible students who enroll

时间窗: Within a 12-month period

Percentage of enrolled participants who attend 5/6 intervention sessions

时间窗: During 6-week interventions

次要结局

  • Depressive Symptoms(At baseline, 6 weeks after, and 32 weeks after)
  • Clinical Depression(At baseline, 6 weeks after, and 32 weeks after)
  • Mindful Attention(At baseline, 6 weeks after, and 32 weeks after)
  • Anxiety(At baseline, 6 weeks after, and 32 weeks after)
  • Perceived Stress(At baseline, 6 weeks after, and 32 weeks after)
  • Social Support(At baseline, 6 weeks after, and 32 weeks after)
  • Self Compassion(At baseline, 6 weeks after, and 32 weeks after)
  • Application of Mindfulness(At baseline, 6 weeks after, and 32 weeks after)
  • Previous Experience with Mindfulness(At baseline, 6 weeks after, and 32 weeks after)
  • Meaning in Life(At baseline, 6 weeks after, and 32 weeks after)
  • Previous Experience with Meditation(At baseline, 6 weeks after, and 32 weeks after)
  • Cortisol stress reactivity(3 visits; baseline, after 6-week intervention, and at 6-month followup)
  • Blood pressure reactivity(3 visits; baseline, after 6-week intervention, and at 6-month followup)
  • Daily mindful attention(During the 6-week group program)
  • Heart rate reactivity(3 visits; baseline, after 6-week intervention, and at 6-month followup)
  • Daily self-compassion(During the 6-week group program)
  • Daily home practice of intervention material(During the 6-week group program)
  • Daily negative events(During the 6-week group program)
  • Daily psychological distress(During the 6-week group program)
  • Depressive Symptoms(At baseline, 6 weeks after, and 32 weeks after)
  • Clinical Depression(At baseline, 6 weeks after, and 32 weeks after)
  • Anxiety(At baseline, 6 weeks after, and 32 weeks after)
  • Perceived Stress(At baseline, 6 weeks after, and 32 weeks after)
  • Social Support(At baseline, 6 weeks after, and 32 weeks after)
  • Meaning in Life(At baseline, 6 weeks after, and 32 weeks after)
  • Mindful Attention(At baseline, 6 weeks after, and 32 weeks after)
  • Self Compassion(At baseline, 6 weeks after, and 32 weeks after)
  • Application of Mindfulness(At baseline, 6 weeks after, and 32 weeks after)
  • Previous Experience with Mindfulness(At baseline, 6 weeks after, and 32 weeks after)
  • Previous Experience with Meditation(At baseline, 6 weeks after, and 32 weeks after)
  • Cortisol stress reactivity(3 visits; baseline, after 6-week intervention, and at 6-month followup)
  • Blood pressure reactivity(3 visits; baseline, after 6-week intervention, and at 6-month followup)
  • Heart rate reactivity(3 visits; baseline, after 6-week intervention, and at 6-month followup)
  • Daily mindful attention(During the 6-week group program)
  • Daily self-compassion(During the 6-week group program)
  • Daily home practice of intervention material(During the 6-week group program)
  • Daily negative events(During the 6-week group program)
  • Daily psychological distress(During the 6-week group program)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Rachel Graham

Professor of Human Development & Family Studies and Colorado School of Public Health

Colorado State University

研究点 (8)

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