singstrong -一项针对长冠肺炎呼吸道和其他常见症状的歌唱和呼吸再训练干预:一项试点研究

R. Cahalan, Ciara Meade, Sarah Mockler
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Demographic and COVID-19 data were collected, and the DePaul Symptom Questionnaire Short Form (DSQ- SF) and COVID-19 Yorkshire Rehab Screen questionnaires were administered. Post-intervention focus groups were also conducted. Results Of 27 (F = 23(85%)) participants recruited, data from 21 who completed at least 10 (50%) classes were analysed. Participants showed significant pre–post-intervention improvements in all breathlessness symptoms (at rest: P < 0.001; dressing: P = 0.01; stairs: P < 0.001), fatigue (P = 0.03), usual activities (P = 0.04), pain/disability (P = 0.03), voice quality (P = 0.01), and communication/cognition (P = 0.04). Pre–post number of instances meeting DSQ-SF criteria for myalgic encephalomyelitis (ME) and chronic fatigue syndrome (CFS) decreased by a net of nine cases (14.3%). No association between COVID-19 hospitalisation status and diagnosis of ME/CFS was identified. 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引用次数: 11

摘要

长冠状病毒(LC)的管理对临床医生来说是一个巨大的挑战。本初步研究评估了呼吸再训练和歌唱方案(SingStrong for LC),以解决LC的常见症状。该研究假设这种干预会改善影响呼吸障碍和参与者健康的症状。方法为期10周,每两周一次的在线课程包括45分钟的正念课程、呼吸再训练、声乐练习和唱歌。对非参与者进行录音,并由在呼吸队列中有经验的训练有素的声乐教练进行。邀请确诊COVID-19并持续出现症状的人参加。收集人口统计学和COVID-19数据,并进行DePaul症状问卷简表(DSQ- SF)和COVID-19约克郡康复筛查问卷。干预后焦点小组也进行了研究。结果在招募的27名(F = 23(85%))参与者中,分析了21名完成至少10节(50%)课程的参与者的数据。受试者在干预前和干预后的所有呼吸困难症状均有显著改善(静止时:P < 0.001;敷料:P = 0.01;楼梯(P < 0.001)、疲劳(P = 0.03)、日常活动(P = 0.04)、疼痛/残疾(P = 0.03)、语音质量(P = 0.01)、沟通/认知(P = 0.04)。岗前符合DSQ-SF标准的肌痛性脑脊髓炎(ME)和慢性疲劳综合征(CFS)病例数净减少了9例(14.3%)。未发现COVID-19住院状况与ME/CFS诊断之间的关联。来自8名参与者的定性反馈是压倒性的积极,所有人都报告呼吸和总体健康状况有所改善。结论:SingStrong项目有望成为LC患者的一种可行的治疗选择。未来的研究需要进一步调查这种干预措施的有效性。
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SingStrong—A singing and breathing retraining intervention for respiratory and other common symptoms of long COVID: A pilot study
Background Management of Long COVID (LC) is hugely challenging for clinicians. This pilot study evaluated a breathing retraining and singing programme (SingStrong for LC) to address common LC symptoms. The study hypothesized that this intervention would improve symptoms impacting disordered breathing and participant wellbeing. Methods The 10-week, bi-weekly online programme was comprised of a 45-min class of mindfulness, breathing retraining, vocal exercises, and singing. Sessions were recorded for non-attenders and conducted by a trained vocal coach experienced in respiratory cohorts. Persons with a confirmed COVID-19 diagnosis and persisting symptoms were invited to participate. Demographic and COVID-19 data were collected, and the DePaul Symptom Questionnaire Short Form (DSQ- SF) and COVID-19 Yorkshire Rehab Screen questionnaires were administered. Post-intervention focus groups were also conducted. Results Of 27 (F = 23(85%)) participants recruited, data from 21 who completed at least 10 (50%) classes were analysed. Participants showed significant pre–post-intervention improvements in all breathlessness symptoms (at rest: P < 0.001; dressing: P = 0.01; stairs: P < 0.001), fatigue (P = 0.03), usual activities (P = 0.04), pain/disability (P = 0.03), voice quality (P = 0.01), and communication/cognition (P = 0.04). Pre–post number of instances meeting DSQ-SF criteria for myalgic encephalomyelitis (ME) and chronic fatigue syndrome (CFS) decreased by a net of nine cases (14.3%). No association between COVID-19 hospitalisation status and diagnosis of ME/CFS was identified. Qualitative feedback from eight participants was overwhelmingly positive with all reporting improvements in breathing and general well-being. Conclusion The SingStrong programme shows promise as a viable treatment option for LC sufferers. Future studies are required to further investigate the efficacy of this intervention.
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