针对监狱在押男性的自我效能增强型减酒干预:APPRAISE 可行性试点 RCT。

Aisha Holloway, Gillian Waller, Jennifer Ferguson, Victoria Guthrie, Jamie Brian Smith, Joanne Boyd, Sharon Mercado, Jessica Rees, Richard Anthony Parker, Andrew Stoddart, Jeremy W Bray, Simon Coulton, Kate Hunt, Gertraud Stadler, Arun Sondhi, Pam Smith, Rosie Stenhouse, Philip Conaglen, Aziz Sheikh, Dorothy Newbury-Birch
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引用次数: 0

摘要

背景:多达 70% 的还押犯人承认在犯罪入狱时受到酒精的影响。为某些人群提供有关饮酒的支持和建议是有效的。对于还押候审的男性囚犯,这方面的证据很少:试行研究措施和评估方法,以评估未来开展明确的多中心、务实、平行小组、随机对照试验的可行性:设计:一项双臂、平行小组、个人随机试验研究,研究内容为提高自我效能的社会心理酒精干预措施,以降低还押候审男性在狱中和解放后的酒精消费水平:地点:苏格兰和英格兰的两所监狱:干预措施:APPRAISE 干预方法包括四个步骤:第 1 步:1 × 40 分钟的面对面课程,由监狱中经过培训的 "Change Grow Live "从业人员实施。第 2、3 和 4 步:在解放后的第 3、7 和 21 天或尽可能接近解放后的第 3、7 和 21 天,通过电话进行 20 分钟的治疗。对照组:评估、筛查和转介酒精支持方案:主要结果测量指标:招募率和保留率、随访完成情况、12 个月的结果测量指标以及提供的干预措施。试点研究的主要结果是时间点 2 之前 28 天内的饮酒量,使用扩展的酒精使用障碍识别测试 C 进行评估:在两个研究地点接触的 182 名还押男子中,132 人被随机分配(英格兰 90 人;苏格兰 42 人),其中英格兰 46 人被随机分配到干预措施,44 人被随机分配到常规护理;苏格兰 22 人被随机分配到干预措施,20 人被随机分配到常规护理。共进行了 53 次狱中干预。解放后第 3 天进行了一次干预,第 7 天没有进行干预,第 21 天进行了一次干预。12 个月后,在 132 名随机参与者中,有 18 人(13%)接受了随访,53 人(40%)未获解放;47 人(36%)无法联系,14 人(11%)已获释但下落不明。基线数据完整率为 96%,12 个月数据完整率为 8%。过程评估报告称,干预措施的可接受性良好,并确定了支持实施的时间、能力和空间投资。经济研究为如何评估与实施 APPRAISE 干预措施相关的成本提供了指导,可在更大范围内应用:未发现不良事件或副作用:结论:未来有可能开展一项明确的试验,但前提是必须解决后续机制问题,以及全面获取累犯和健康数据。未来与缓刑服务机构的合作可以提供机会,开发一个强大的程序和系统,以优化解放后的跟进工作。建议提供专用资源,支持在监狱内外实施干预措施:2019年发现的冠状病毒疾病影响了招募和后续工作,进入监狱受到限制。我们无法实施解放后的干预措施。我们没有将缓刑服务或其他机构纳入试验:该试验注册为当前对照试验 ISRCTN36066:该奖项由国家健康与护理研究所(NIHR)公共卫生研究计划资助(NIHR奖项编号:17/44/11),全文发表于《公共卫生研究》第12卷第11期。更多获奖信息,请参阅 NIHR Funding and Awards 网站。
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A self-efficacy enhancement alcohol reduction intervention for men on-remand in prison: the APPRAISE feasibility pilot RCT.

Background: As many as 70% of remand prisoners have admitted to being under the influence of alcohol when committing the crime leading to their imprisonment. Providing support and advice regarding alcohol consumption can be effective in some groups of people. There is little evidence regarding this for men on remand in prison.

Objective: To pilot the study measures and evaluation methods to assess the feasibility of conducting a future definitive multicentre, pragmatic, parallel group, randomised controlled trial.

Design: A two-arm, parallel group, individually randomised pilot study of a self-efficacy-enhancing psychosocial alcohol intervention to reduce levels of alcohol consumption for males on remand in prison and on liberation.

Setting: Two purposively selected prisons in Scotland and England.

Participants: Adult men on remand in prison with an Alcohol Use Disorders Identification Test score of ≥ 8.

Intervention: The APPRAISE intervention delivery comprised four steps: Step 1: 1 × 40-minute face-to-face session, delivered by a trained practitioner from Change Grow Live in prison. Steps 2, 3 and 4: 20-minute sessions conducted by phone, on or as close as possible to days 3, 7 and 21 post liberation. Control: assessment, screening and referral onto further alcohol support options.

Main outcome measures: Recruitment and retention rates, completion of follow-ups, outcome measures at 12 months and interventions delivered. The primary outcome for the pilot study was alcohol consumed in the 28 days prior to Time Point 2, assessed using the extended Alcohol Use Disorders Identification Test-C.

Results: Of 182 men on remand approached across two study sites, 132 were randomised (90 in England; 42 in Scotland) with 46 randomised to intervention and 44 to care as usual in England and 22 randomised to intervention and 20 to care as usual in Scotland. A total of 53 in-prison interventions were delivered. One day-3 post-liberation intervention was delivered, no day-7 and one day-21. At 12 months, of 132 randomised, 18 (13%) were followed up, 53 (40%) were not liberated; 47 (36%) were uncontactable and 14 (11%) had been released but could not be located. Data completeness was 96% at baseline and 8% at 12 months. The process evaluation reported good acceptability of the intervention with investment in time, capacity and space to support implementation identified. The economic study produced guidance on how to assess costs associated with implementing the APPRAISE intervention which could be applied more broadly.

Harms: No adverse events or side effects were noted.

Conclusions: A future definitive trial would be possible, but only if follow-up mechanisms can be addressed as well as full access to recidivism and health data. Collaboration with the probation service in future could offer the opportunity to develop a robust process and system to optimise follow-up post liberation. Dedicated resources to support the intervention delivery both in and out of the prison setting are recommended.

Limitations: Coronavirus disease discovered in 2019 impacted recruitment and follow-up, with access to prisons restricted. We were unable to deliver the post-liberation element of the intervention. We did not include probation services or other agencies in the trial.

Trial registration: This trial is registered as Current Controlled Trials ISRCTN36066.

Funding: This award was funded by the National Institute for Health and Care Research (NIHR) Public Health Research programme (NIHR award ref: 17/44/11) and is published in full in Public Health Research; Vol. 12, No. 11. See the NIHR Funding and Awards website for further award information.

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