跳至主要内容
临床试验/NCT06743282
NCT06743282Enrolling By Invitation不适用

Senyo Health App - Connecting Primary Care to Substance Use Disorder Treatment Using a Telehealth Collaborative Care Platform

Mayo Clinic2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年9月22日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
Enrolling By Invitation
发起方
Mayo Clinic
入组人数
60
试验地点
2
主要终点
Brief Substance Craving Scale (BSCS)

研究概览

简要总结

The purpose of this study is to examine the barriers, facilitators, and optimal processes for implementing a digitally enhanced screening, brief intervention, and referral to treatment (SBIRT) model for Substance Use Disorder SUD treatment among Mayo primary care clinics.

研究设计

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

入排标准

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

入选标准

  • Ability to read, write, and understand English
  • Minimum DAST (1+), audit-C score (3+)
  • Access and willingness to use a mobile device for asynchronous (text) and synchronous (video) engagement with care.
  • Access to or willingness to obtain a Primary care provider at a participating Mayo Clinic site;
  • Eligibility determined by ASAM Assessment

排除标准

  • Diagnosed personality pathology as the primary presenting concern based on clinical judgment, severe cognitive impairment (e.g., intellectual disability or dementia), or psychosis
  • Inability to actively participate in and learn from psychotherapeutic interaction based on clinical evaluation and clinical judgment
  • Needing a higher level of mental health care as demonstrated by ASAM32 assessment.
  • Decline to answer suicidality questions.
  • Already admitted into or about to initiate treatment in another addiction treatment program.
  • Currently attending High School.

研究组 & 干预措施

Senyo

Experimental

Subjects to the Senyo group will begin receiving intervention immediately, and will move to the follow-up phase after 12 weeks.

干预措施: Senyo App (Behavioral)

Senyo

Experimental

Subjects to the Senyo group will begin receiving intervention immediately, and will move to the follow-up phase after 12 weeks.

干预措施: Follow-up (Behavioral)

结局指标

主要结局

Brief Substance Craving Scale (BSCS)

时间窗: Baseline, weekly for 12 weeks, 4 months, 5 months, 6 months

The Brief Substance Craving Scale is a 16 item, self-report instrument that assesses craving for substances of abuse over a 24 hour period. Intensity and frequency of craving are recorded on a five-point Likert scale, with 0 = Not at all, 1 = Slight, 2 = Moderate, 3 = Considerable, and 4 = Extreme.

Timeline Follow Back

时间窗: Baseline, weekly for 12 weeks, 4 months, 5 months, 6 months

Timeline Follow Back is an assessment to document substance use over a specific period of time

Brief Substance Craving Scale (BSCS)

时间窗: Baseline, weekly for 12 weeks, 4 months, 5 months, 6 months

The Brief Substance Craving Scale is a 16 item, self-report instrument that assesses craving for substances of abuse over a 24 hour period. Intensity and frequency of craving are recorded on a five-point Likert scale, with 0 = Not at all, 1 = Slight, 2 = Moderate, 3 = Considerable, and 4 = Extreme.

次要结局

  • Generalized Anxiety Disorder-7 (GAD-7)(Baseline, weekly for 12 weeks, 4 months, 5 months, 6 months)
  • Patient Health Questionnaire-9 (PHQ-9)(Baseline, weekly for 12 weeks, 4 months, 5 months, 6 months)

研究者

发起方
Mayo Clinic
申办方类型
Other
责任方
Principal Investigator
主要研究者

Tyler S. Oesterle

Principal Investigator

Mayo Clinic

研究点 (2)

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