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基于心理应对方式的脑震荡康复方法的可行性:一项随机对照试验。

Feasibility of Concussion Rehabilitation Approaches Tailored to Psychological Coping Styles: A Randomized Controlled Trial.

机构信息

Department of Psychology, University of British Columbia, Vancouver, British Columbia, Canada; Rehabilitation Research Program, Vancouver Coastal Health Research Institute, Vancouver, British Columbia, Canada.

Centre for Clinical Epidemiology and Evaluation, Vancouver Coastal Health Research Institute, Vancouver, British Columbia, Canada.

出版信息

Arch Phys Med Rehabil. 2022 Aug;103(8):1565-1573.e2. doi: 10.1016/j.apmr.2021.12.005. Epub 2021 Dec 28.

Abstract

OBJECTIVE

To evaluate the feasibility of a clinical trial involving participants with concussion randomized to treatments designed to address fear avoidance or endurance coping, which are risk factors for disability. A secondary objective was to evaluate whether each treatment could affect selective change on targeted coping outcomes.

DESIGN

Randomized controlled trial.

SETTING

Outpatient concussion clinics.

PARTICIPANTS

Adults (N=73, mean age=42.5y) who had persistent postconcussion symptoms and high avoidance or endurance behavior were enrolled at a mean of 12.9 weeks post injury. Ten participants did not complete treatment.

INTERVENTIONS

Participants were randomized to an interdisciplinary rehabilitation program delivered via videoconferencing and tailored to avoidance coping (graded exposure therapy [GET]) or endurance coping (operant condition-based pacing strategies plus mindfulness training [Pacing+]).

MAIN OUTCOME MEASURES

Feasibility outcomes included screening efficiency, accrual, credibility, treatment fidelity, adherence, and retention. Avoidance was measured with the Fear Avoidance Behavior after Traumatic Brain Injury Questionnaire and endurance behavior with the Behavioral Response to Illness Questionnaire.

RESULTS

Screening efficiency, or the proportion of clinic patients who were assessed for eligibility, was 44.5% (275 of 618). A total of 65.8% (73 of 111) of eligible patients were randomized (37 to GET, 36 to Pacing+), meeting accrual targets; 91.7% (55 of 60) of participants perceived treatment as credible. Therapists covered a mean of 96.8% of essential prescribed elements, indicating excellent fidelity. The majority (71.2%; 47 of 66) of participants consistently attended treatment sessions and completed between-session homework. Retention was strong, with 65 of 73 (89%) randomized participants completing the outcome assessment. GET was associated with greater posttreatment reductions in avoidance behavior compared with Pacing+ (Cohen's d, 0.81), whereas the treatment approach-specific effect of Pacing+ on endurance behavior was less pronounced (Cohen's d, 0.39).

CONCLUSIONS

These findings support a future efficacy-focused clinical trial. GET has the potential to selectively reduce fear avoidance behavior after concussion, and, via this mechanism, to prevent or reduce disability.

摘要

目的

评估一项临床试验的可行性,该试验涉及将随机分组接受旨在解决恐惧回避或耐力应对的治疗的脑震荡参与者,这是导致残疾的风险因素。次要目标是评估每种治疗方法是否可以针对特定的应对结果进行选择性改变。

设计

随机对照试验。

地点

门诊脑震荡诊所。

参与者

成年人(N=73,平均年龄 42.5 岁),他们在受伤后 12.9 周左右出现持续性脑震荡后症状和高回避或耐力行为。10 名参与者未完成治疗。

干预措施

参与者被随机分配到通过视频会议提供的跨学科康复计划中,并根据回避应对(分级暴露治疗[GET])或耐力应对(操作性条件基于的 pacing 策略加正念训练[Pacing+])进行量身定制。

主要结果测量

可行性结果包括筛选效率、入组、可信度、治疗保真度、依从性和保留率。回避行为通过创伤性脑损伤后恐惧回避行为问卷测量,耐力行为通过疾病行为反应问卷测量。

结果

筛选效率,即评估符合条件的门诊患者的比例,为 44.5%(275/618)。共有 65.8%(73/111)的合格患者被随机分组(37 人接受 GET,36 人接受 Pacing+),达到了入组目标;91.7%(55/60)的参与者认为治疗可信。治疗师涵盖了规定要素的平均 96.8%,表明保真度很高。大多数(71.2%;47/66)参与者始终参加治疗课程并完成了课程之间的作业。保留率很强,73 名随机参与者中有 65 名(89%)完成了结果评估。与 Pacing+相比,GET 治疗后回避行为的减少幅度更大(Cohen's d,0.81),而 Pacing+对耐力行为的治疗方法特异性影响则不太明显(Cohen's d,0.39)。

结论

这些发现支持未来以疗效为重点的临床试验。GET 有可能选择性地减少脑震荡后的恐惧回避行为,并通过这种机制预防或减少残疾。

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