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临床试验/NCT06022107
NCT06022107已完成不适用

Piloting a Novel Social Support Intervention for Addiction Recovery

Yale University2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2024年1月26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
30
试验地点
2
主要终点
Recruitment Feasibility

研究概览

简要总结

The purpose of this research study is to determine whether using a web-based intervention is feasible, acceptable, and helpful for people who engage in hazardous alcohol use and want to cut down or quit.

详细描述

This pilot study will determine the feasibility and acceptability of a novel online social support intervention (Let's Do Addiction Recovery Together!, abbreviated as LDART) that uses pre-recorded videos created by members of recovery support services to help individuals in early recovery from hazardous alcohol use sustain motivation during recovery and introduce them to freely available recovery support services in the community. The investigators will recruit participants to use the web-based intervention daily for a month; they will also fill in questionnaires about their substance use and engagement with recovery support services at the beginning and end of the study to determine preliminary efficacy.

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

  • 18 years of age or older
  • Is at the time of study participation residing in Connecticut, USA
  • Is fluent in English and has a 6th grade reading level or higher
  • Alcohol Use Disorders Identification Test (AUDIT) score of ≥8
  • Has had at least one heavy drinking day in the past month
  • Has some desire to cut down or quit their alcohol use
  • Has a smartphone or computer with access to internet

排除标准

  • Has vulnerable population status (e.g., pregnant people, prisoners)
  • Is at the time of study participation receiving in-patient psychiatric treatment involving hospitalization

结局指标

主要结局

Recruitment Feasibility

时间窗: Baseline

Feasibility of recruitment is measured as the number of adults who consent to study participation divided by the number of months the trial recruits for.

Retention Feasibility

时间窗: One-month post-intervention (Day 56)

Retention rate is calculated as the number of participants who complete the study divided by the number of participants who consented to participating in the study.

Intervention Acceptability (Engagement With Intervention)

时间窗: Duration of intervention (Days 1-28)

Acceptability is calculated as the number of nights participants login to LDART within the 28-day window.

Intervention Acceptability (Subjective Experience)

时间窗: Post-intervention (Day 28)

Acceptability is measured with a 9-item self-report acceptability assessment questionnaire. This comprises questions regarding the motivational and supportive properties of the content, perceptions on the frequency of engaging with the intervention, and whether they enjoyed using the intervention. Each question is rated on a 5-point Likert scale, where higher values indicate greater acceptability. There will also be two open-ended questions for participants to indicate what they liked and did not like about the intervention and ways to improve it. Data reported here reflects percentage of participants who answered "agree" or "strongly agree" to the question: "I would recommend LDART to someone trying to cut down or quit drinking".

次要结局

  • Percentage of Drinking Days Per Month(Day 0 (Pre-intervention), 28 (Post-intervention), and 56 (1-month post-intervention))
  • Percentage of Heavy Drinking Days Per Month(Day 0 (Pre-intervention), 28 (Post-intervention), and 56 (1-month post-intervention))
  • Hours Spent Engaging With Recovery Support Services(Day 0 (Pre-intervention), 28 (Post-intervention), and 56 (1-month post-intervention))
  • World Health Organization Quality of Life - Brief Version(Day 0 (Pre-intervention), 28 (Post-intervention), and 56 (1-month post-intervention))
  • Brief Assessment of Recovery Capital(Day 0 (Pre-intervention), 28 (Post-intervention), and 56 (1-month post-intervention))

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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