跳至主要内容
临床试验/NCT06056674
NCT06056674进行中(未招募)不适用

Unified Protocol for Preventing Emotional and Academic Challenges in Education (U-PEACE) Randomized Controlled Trial

University of Miami1 个研究点 分布在 1 个国家目标入组 72 人开始时间: 2023年10月5日最近更新:
适应症
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
72
试验地点
1
主要终点
Client Satisfaction Questionnaire (CSQ)

研究概览

简要总结

The purpose of the study is to evaluate the feasibility and effectiveness of a program for high school students with emotional and academic challenges U-PEACE and gaining feedback on that program.

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
None

入排标准

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

入选标准

  • Adolescents between the ages of 13 and 18 years at the time of enrollment, who:
  • display depressive symptoms above the clinical cut-off of 9 or above on the Patient Health Questionnaire-8 (PHQ-8),
  • display elevated anxiety symptoms of 10 or above on the Generalized Anxiety Disorder 7-item Scale (GAD-7; Spitzer et al., 2006),
  • are enrolled at the target High Schools (HS),
  • have expressed interest in participating in the study, and
  • have a caregiver who is available to sign study consent forms (if under 18 years of age)
  • Adolescents must be, or are willing to be, consented to receive services through School Health Initiative (SHI) (i.e., SHI consent). If they are under 18 years of age, their caregiver must provide consent.
  • Adolescents and caregivers are able to complete all study procedures in English or Spanish.
  • Individuals who are 18 years or older.
  • Individuals who are currently employed at the target HSs.
  • Individuals who are able to speak, read, and understand English.

排除标准

  • The following individuals may be excluded at any time (e.g., before consent, after being enrolled).
  • Individuals who do not wish to participate in this study and/or who are not able to read and understand the consent/assent.
  • Individuals with self- or caregiver-reported history of seizures, neurological problems, autism spectrum disorder, substance use disorder, or serious mental illness (e.g., schizophrenia), and any indicator of a significant cognitive delay that would make U-PEACE inappropriate (e.g., full-time special education placement)
  • Individuals with current anxiety or depressive symptoms or active suicidality at levels where more intensive services (e.g., day treatment, inpatient) would be warranted (e.g., hospitalization for suicidal behavior in the last 12 months).
  • Ineligible adolescents will be provided referrals to medical providers at the SHI, community agencies contracted with the Miami-Dade County Public Schools (M-DCPS) Office of Mental Health Services or emergency room settings, as appropriate.
  • Unclear cases will be reviewed by the PI and Director of the SHI, Co-I Lisa Gwynn, D.O.

研究组 & 干预措施

Services As Usual (SAU) Group

Active Comparator

Participants in this group will receive service as usual (study participation to last approximately 13 weeks).

干预措施: SAU (Behavioral)

U-PEACE Group

Experimental

Participants in this group will receive the U-PEACE intervention (study participation to last approximately 13 weeks).

干预措施: U-PEACE Intervention (Behavioral)

结局指标

主要结局

Client Satisfaction Questionnaire (CSQ)

时间窗: Mid (approximately week 4)

Total Scores range from 8 to 32, with higher scores indicating greater client satisfaction. The CSQ support used to evaluate satisfaction with a particular intervention, client self-efficacy and the likelihood of recommending the intervention to others.

Adherence to U-PEACE, as Measured by Homework Completion

时间窗: At all group sessions (up to 9 weeks)

Adherence to U-PEACE will be measured by the overall number of homework assignments completed.

Change in Revised Children's Anxiety and Depression Scale - Child Revised Short Version (RCADS-C-S)

时间窗: At baseline, mid (approximately week 4), post (approximately week 9) and 1-month follow-up (approximately week 13)

The Change in Revised Children's Anxiety and Depression Scale - Child Revised Short Version (RCADS-25) is 25-item self-reported scale measuring symptoms of anxiety and depression in youth. Items are rated on a 4-point scale from 1 (Never) to 4 (always) with total composite scores ranging from 0 to 75. A score of 70 or higher indicates high severity.

Change in Generalized Anxiety Disorder 7-item Scale (GAD-7)

时间窗: At baseline, mid (approximately week 4), post (approximately week 9) and 1-month follow-up (approximately week 13)

GAD-7 evaluates core anxiety concerns across a 7-item self-report measure. Items are rated using a 4-point Likert scale from 0 (not at all) to 3 (nearly every day). It yields a total score and a rating of impairment

Change in Patient Health Questionnaire 9-item Scale (Modified for Major Depressive Disorder in Adolescents; PHQ-9M)

时间窗: At baseline, mid (approximately week 4), post (approximately week 9) and 1-month follow-up (approximately week 13)

PHQ-9 evaluates core depression symptoms across 9 items. Items are rated on a 4-point Likert scale from 0 (not at all) to 3 (nearly every day)

Change in Adolescent Academic Problems Checklist (AAPC)

时间窗: At baseline, mid (approximately week 4), post (approximately week 9) and 1-month follow-up (approximately week 13)

Scores on each item range from 0 to 3, with higher scores indicating more academic problems.

Therapeutic Alliance Scale for Children, Revised (TASC-R)

时间窗: Mid (approximately week 4)

Scores on each item range from 1 (not true) to 4 (very much true). This scale measures the perceived therapeutic alliance between child and therapist.

Top Problems Assessment - Child Report as measured by Likert Scale

时间窗: Up to 13 weeks

The Top Problems assessment is used to identify self-reported target problems for treatment and track changes in problem severity over time. Identified top problem statements are rated on Likert scale from 0 (not at all a problem) to 10 (a huge problem).

Adherence to U-PEACE, as Measured by Session Attendance

时间窗: At all group sessions (up to 9 weeks)

Adherence to U-PEACE will be measured by the overall number of sessions attended.

次要结局

  • Change in Affective Reactivity Scale (ARI)(At baseline, mid (approximately week 4), post (approximately week 9) and 1-month follow-up (approximately week 13))
  • Change in Distress Tolerance Scale (DTS)(At baseline, mid (approximately week 4), post (approximately week 9) and 1-month follow-up (approximately week 13))
  • School Achievement, as measured by report card(Up to approximately 13 weeks)
  • Change in Child Anxiety Impact Scale-Academic Subscale (CAIS-AS)(At baseline, mid (approximately week 4), post (approximately week 9) and 1-month follow-up (approximately week 13))
  • School Achievement, as measured by attendance(Up to approximately 13 weeks)

研究者

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

Jill May Ehrenreich

Professor

University of Miami

研究点 (1)

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