Wilson Jon, Cestaro Viktoria, Charami-Roupa Eirini, Clarke Timothy, Dunne Aoife, Gee Brioney, Jarrett Sharon, Katangwe-Chigamba Thando, Laphan Andrew, McIvor Susie, Meiser-Stedman Richard, Murdoch Jamie, Rhodes Thomas, Seeley Carys, Shepstone Lee, Turner David, Wilkinson Paul
Research and Development, Norfolk and Suffolk NHS Foundation Trust, Norwich, UK.
Norwich Medical School, University of East Anglia, Norwich, UK.
Health Soc Care Deliv Res. 2024 Dec;12(48):1-121. doi: 10.3310/GTRV6410.
As milder cases of adolescent depression do not meet treatment thresholds for specialist mental health services, young people often receive support from non-qualified professionals in third-sector/voluntary agencies. Early psychological interventions to meet growing demand with limited resources are crucial.
The study aimed to explore the effectiveness and cost effectiveness of interpersonal counselling for adolescents by (1) assessing the feasibility and acceptability of trial procedures; (2) exploring the delivery of, and differences between, interpersonal counselling for adolescents and treatment as usual; (3) evaluating the extent of contamination of the control arm and if it should be mitigated against in a future trial; and (4) investigating whether the interval estimate of benefit of interpersonal counselling for adolescents over treatment as usual in depression post treatment includes a clinically significant effect.
This was a feasibility randomised controlled trial. Non-qualified professionals from non-specialist mental health services received interpersonal counselling for adolescent training. Participants were randomised to receive either interpersonal counselling for adolescents plus treatment as usual or treatment as usual only. Assessments occurred at baseline and were followed up at weeks 5, 10 and 23. A health economics component was included to inform the design of the economic evaluation in a future study. A process evaluation examined implementation of the intervention across settings, acceptability and contamination. Interviews, observations and focus groups were analysed using thematic analysis. Session recordings were analysed using conversation analysis.
The trial was conducted in 13 non-speicialist mental health services across Norfolk and Suffolk.
Help-seeking adolescents aged 12-18 years with mild depression as the primary difficulty were eligible to participate. Comorbid presentations were not an exclusion criterion. Of a target of 60, 16 participants were randomised, and 2 participants withdrew following study suspensions related to COVID-19. Of the remaining 14 participants, 7 received an intervention, with 3 receiving interpersonal counselling for adolescents and 4 receiving treatment as usual. The rest either disengaged, withdrew or were signposted.
Participants were randomised to receive either interpersonal counselling for adolescents plus treatment as usual or treatment as usual only.
The primary outcome was the Revised Children's Anxiety and Depression Scale, although the proposed study was not designed to assess efficacy. The primary output of the feasibility trial was to design a subsequent full-scale trial.
Feasibility outcomes did not meet the estimated progression criteria. Despite efforts to increase referrals, the 80% recruitment rate was not achieved. Interpersonal counselling for adolescents' attendance rates at 10 weeks were less than the 70% progression criteria estimation, impacting intervention feasibility. Retention was high, with 85.7% of participants reaching 23-week follow-up. The health economic measures appeared to perform well and were completed. Implementation and theoretical fidelity of interpersonal counselling for adolescents were analysed from four participant recordings. Adherence to the principles of interpersonal counselling for adolescents was identified, with 100% satisfactory fidelity and no indication of contamination in the control arm. The two interventions were clinically non-significant due to the study being underpowered.
The feasibility of the randomised controlled trial was impacted by COVID-19. Services had to change standard practices, disrupting trial procedures. Challenges were identified when implementing a randomised controlled trial in non-specialist services.
Findings indicate a randomised controlled trial of interpersonal counselling for adolescents in non-specialist services is not feasible, yet the data collection and outcome measures were suitable. COVID-19 challenges, sites' lack of familiarity with research procedures and the research team's unfamiliarity with how different early intervention services operate led to challenges. High staff shortages, turnover and inconsistent training could have been considered. This study demonstrated the difficulties in conducting a randomised controlled trial in this service setting. Further work is needed to improve the feasibility of conducting such trials before they are attempted in future.
This trial is registered as ISRCTN82180413.
This award was funded by the National Institute for Health and Care Research (NIHR) Health and Social Care Delivery Research programme (NIHR award ref: 17/112/16) and is published in full in ; Vol. 12, No. 48. See the NIHR Funding and Awards website for further award information.
由于青少年抑郁症的轻症病例未达到专科心理健康服务的治疗阈值,年轻人常常从第三部门/志愿机构的非专业人员那里获得支持。在资源有限的情况下,通过早期心理干预来满足不断增长的需求至关重要。
本研究旨在探讨青少年人际咨询的有效性和成本效益,具体包括:(1)评估试验程序的可行性和可接受性;(2)探究青少年人际咨询的实施情况以及与常规治疗之间的差异;(3)评估对照组的沾染程度以及在未来试验中是否应予以减轻;(4)调查青少年人际咨询相较于常规治疗在治疗后抑郁症方面的获益区间估计是否包含具有临床意义的效果。
这是一项可行性随机对照试验。来自非专科心理健康服务机构的非专业人员接受了青少年人际咨询培训。参与者被随机分配,要么接受青少年人际咨询加常规治疗,要么仅接受常规治疗。在基线时进行评估,并在第5、10和23周进行随访。纳入了一个卫生经济学部分,为未来研究中的经济评估设计提供信息。进行了一项过程评估,以检查干预措施在不同环境中的实施情况、可接受性和沾染情况。使用主题分析法对访谈、观察和焦点小组进行分析。使用会话分析法对会话记录进行分析。
该试验在诺福克和萨福克的13个非专科心理健康服务机构中进行。
以轻度抑郁症为主要困难的12 - 18岁寻求帮助的青少年有资格参与。共病表现不是排除标准。目标招募60人,16名参与者被随机分组,2名参与者在与COVID - 19相关的研究暂停后退出。在其余14名参与者中,7人接受了干预,其中3人接受青少年人际咨询,4人接受常规治疗。其余参与者要么脱离、退出,要么被转介。
参与者被随机分配,要么接受青少年人际咨询加常规治疗,要么仅接受常规治疗。
主要结局是修订后的儿童焦虑和抑郁量表,尽管本拟研究并非旨在评估疗效。可行性试验的主要产出是设计后续的全面试验。
可行性结果未达到估计的进展标准。尽管努力增加转诊,但未达到80%的招募率。青少年人际咨询在10周时的出勤率低于70%的进展标准估计,影响了干预的可行性。保留率较高,85.7%的参与者完成了23周的随访。卫生经济措施似乎运行良好并已完成。从四份参与者记录中分析了青少年人际咨询的实施情况和理论保真度。确定了对青少年人际咨询原则的遵循情况,保真度100%令人满意,且对照组无沾染迹象。由于研究效能不足,两种干预措施在临床上无显著差异。
随机对照试验的可行性受到COVID - 19的影响。服务机构不得不改变标准做法,扰乱了试验程序。在非专科服务机构实施随机对照试验时发现了一些挑战。
研究结果表明,在非专科服务机构中对青少年进行人际咨询的随机对照试验不可行,但数据收集和结局指标是合适的。COVID - 19带来的挑战、各机构对研究程序的不熟悉以及研究团队对不同早期干预服务运作方式的不熟悉导致了诸多困难。本可考虑工作人员严重短缺、人员流动和培训不一致等问题。这项研究证明了在这种服务环境中进行随机对照试验的困难。在未来尝试此类试验之前,需要进一步开展工作以提高其可行性。
本试验注册为ISRCTN82180413。
本奖项由英国国家卫生与保健研究机构(NIHR)卫生与社会保健交付研究项目资助(NIHR奖项编号:17/112/16),全文发表于《》第12卷,第48期。有关更多奖项信息,请参阅NIHR资金与奖项网站。