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临床试验/NCT05532683
NCT05532683已完成不适用

Development and Feasibility of a Lifestyle Group Intervention for Youth at Clinical High Risk for Psychosis

University of California, Los Angeles2 个研究点 分布在 1 个国家目标入组 9 人开始时间: 2023年4月4日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
9
试验地点
2
主要终点
Change in Subjective Stress

研究概览

简要总结

The present study will assess the feasibility and social validity of an adjunctive health promotion group for youth and clinical high risk for psychosis (CHR-P). Youth participating in treatment at the Center for the Assessment and Prevention of Prodromal Sates (CAPPS) will be invited to participate in a weekly, adjunctive, closed psychoeducation group focused on sharing health promotion strategies and increasing health behaviors (e.g. improved sleep habits, increased participation in physical activity).

The aim of the group will be to provide psychoeducation on lifestyle risk and protective factors for youth at risk for psychosis (i.e. experiencing subthreshold psychosis symptoms). Topics covered will include psychoeducation, goal setting, stress management, sleep, physical activity, substance use, and nutrition. Evidence-based strategies to decrease risk factors and promote protective lifestyle factors for mental illness will be reviewed. Group leaders will utilize a motivational interviewing approach to facilitate the group.

The group will complete nine weekly group sessions. The goal of our research is to 1) determine the feasibility of a novel group-based health promotion intervention, 2) assess the social validity of the group, 3) measure the effects of the intervention on stress, sleep, physical activity, substance use, and nutrition, and 4) measure preliminary effects on symptoms and functioning.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

年龄范围
13 Years 至 17 Years(Child)
性别
All
接受健康志愿者

入选标准

  • between 13 and 17 years old
  • able to sign and provide informed consent (assent for minors)
  • meet criteria for CHR-P using the Structured Interview for Psychosis-Risk Syndromes (SIPS).
  • Must have a primary caregiver willing to participate who speaks fluent English

排除标准

  • current or lifetime DSM-5 psychotic disorder
  • impaired intellectual functioning (IQ <65)
  • history of neurological disorder
  • traumatic brain injury (≥7 on TBI screening tool)
  • significant substance use that makes CHR-P diagnosis ambiguous

结局指标

主要结局

Change in Subjective Stress

时间窗: Change from baseline (pre-intervention) to 9- week post-intervention

Participant subjective stress will be assessed via the 10-item self-report Perceived Stress Scale ( PSS; Cohen et al., 1983).The PSS consists of 10 items rated 0= Never to 4= Very Often, with a higher score suggesting more stress.

Change in Diet

时间窗: Change from baseline (pre-intervention) to 9- week post-intervention

Change in diet will be measured on the ASA24. This dietary assessment uses 24-hour recall to assess nutrition quality and provides measure of total energy intake and macronutrients.

Participant Recruitment and Retention

时间窗: Across Intervention: 9 weeks

Feasibility will be measured by recruitment (participants approached/ participants enrolled) and retention (participants enrolled/ participants completed at least two-thirds of the intervention). Feasibility data will be summarized by the percent recruited, the percent retained by group and the mean and median number of sessions attended by group. The percent who attended each session by group over time will also be reported. Good feasibility will be defined as 70% of those enrolled completing at least two-thirds of the intervention (6 sessions).

Change in Physical Activity

时间窗: Change from baseline (pre-intervention) to 9- week post-intervention

The mean profile from baseline to post-treatment for physical activity as assessed by the International Physical Activity Questionnaire - Short Form (IPAQ-SF; Craig et al., 2017). Activity levels will be self-report.

Change Sleep Habits

时间窗: Change from baseline (pre-intervention) to 9- week post-intervention

Sleep will be assessed via self-report on the PROMIS Pediatric Sleep Disturbance scale (Buysse, et al., 2010). The Pediatric Sleep Disturbance Scale consists of 15 items rated 1 = Never, 2 = Almost Never, 3 = Sometimes, 4 = Almost Always, and 5 = Always, with a higher score indicating more sleep disturbance.

Change in Substance Use

时间窗: Change from baseline (pre-intervention) to 9- week post-intervention

Alcohol and drug use will be measured by clinician rated on the Alcohol Use Scale and Drug Use Scale (AUS/DUS; Drake et al., 1996). This measure rates frequency and impairment associated with alcohol and drug use. Alcohol and drug use are rated on both frequency (0= no use to 5= almost daily) and impairment (0= abstinent to 5= dependence with institutionalization). A rating of 3 or higher on impairment corresponds with substance use disorder.

次要结局

  • Social Validity as assessed by the Semi-Structured Interview for Social Validation(9-week post-intervention)

研究者

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

Bernalyn Ruiz-Yu, PhD

Postdoctoral Fellow

University of California, Los Angeles

研究点 (2)

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