Protocol for a randomized clinical trial to confirm the effectiveness of online guided self-help family-based treatment for adolescent anorexia nervosa

IF 2 3区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Contemporary clinical trials Pub Date : 2024-07-04 DOI:10.1016/j.cct.2024.107618
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Abstract

Background

The leading evidence-based treatment for anorexia nervosa (AN) in adolescents is Family-based Treatment (FBT). However, due to the intensive training requirements and lack of practitioners, it is often difficult for families to access FBT. Thus, innovations that improve access to care are needed. A pilot randomized study of a guided self-help version of Family-based Treatment (GSH-FBT) that utilized approximately 1/4 the amount of therapist time compared to FBT found that the approach was acceptable and appeared to achieve similar outcomes. The study protocol detailed in this manuscript compares the efficiency (clinician time) of GSH-FBT to Family-based Treatment via Videoconferencing (FBT-V) in a fully powered study in achieving clinical outcomes through a multi-site randomized clinical trial across the US and Ontario, Canada.

Methods

This study will randomize the families of adolescents ages 12–18 (n = 200) who meet DSM-5 criteria for AN to receive either GSH-FBT or FBT-V. Participants will be randomized to 15 sixty-minute sessions of FBT-V or to 10 twenty-minute sessions of online GSH-FBT. Major assessments will be conducted by a masked assessor at baseline, within treatment, at the end of treatment (EOT), and 6 and 12 months after the end of treatment (EOT). The primary outcomes of this study are changes to body weight and eating disorder cognitions relative to clinician time used (relative efficiency of treatment modality).

Conclusions

The findings of this study may help increase access to care by providing a time efficient, affordable, more scalable intervention for adolescent AN compared to standard FBT.

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一项随机临床试验的方案,以确认基于家庭的在线指导自助治疗对青少年厌食症的有效性。
背景:青少年厌食症(AN)的主要循证治疗方法是家庭治疗(FBT)。然而,由于需要密集的培训和缺乏从业人员,家庭往往难以获得基于家庭的治疗。因此,我们需要创新来改善治疗的可及性。一项关于引导式自助家庭治疗(GSH-FBT)的试验性随机研究发现,与 FBT 相比,GSH-FBT 所占用的治疗师时间约为 FBT 的 1/4 ,这种方法是可以接受的,而且似乎取得了相似的效果。本手稿中详细介绍的研究方案通过在美国和加拿大安大略省进行多站点随机临床试验,比较了 GSH-FBT 和视频会议家庭治疗(FBT-V)的效率(临床医生时间),以取得临床结果:本研究将随机安排符合 DSM-5 AN 标准的 12-18 岁青少年家庭(n = 200)接受 GSH-FBT 或 FBT-V。参与者将随机接受15次60分钟的FBT-V治疗或10次20分钟的在线GSH-FBT治疗。主要评估将由一名蒙面评估员在基线、治疗期间、治疗结束(EOT)以及治疗结束(EOT)后 6 个月和 12 个月进行。本研究的主要结果是体重和进食障碍认知相对于临床医生所用时间的变化(治疗方式的相对效率):本研究的结论:与标准的 FBT 相比,本研究为青少年 AN 提供了一种省时、经济、更可扩展的干预方法,从而有助于提高治疗的可及性。
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来源期刊
CiteScore
3.70
自引率
4.50%
发文量
281
审稿时长
44 days
期刊介绍: Contemporary Clinical Trials is an international peer reviewed journal that publishes manuscripts pertaining to all aspects of clinical trials, including, but not limited to, design, conduct, analysis, regulation and ethics. Manuscripts submitted should appeal to a readership drawn from disciplines including medicine, biostatistics, epidemiology, computer science, management science, behavioural science, pharmaceutical science, and bioethics. Full-length papers and short communications not exceeding 1,500 words, as well as systemic reviews of clinical trials and methodologies will be published. Perspectives/commentaries on current issues and the impact of clinical trials on the practice of medicine and health policy are also welcome.
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