Respiratory biofeedback and psycho-education for patients with post COVID- 19 symptoms and bodily distress: study protocol of the randomized, controlled explorative intervention trial POSITIV.

IF 2 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Trials Pub Date : 2025-04-25 DOI:10.1186/s13063-025-08842-6
Hannah Dinse, Eva-Maria Skoda, Adam Schweda, Christoph Jansen, Kira Schmidt, Margarethe Konik, Hana Rohn, Oliver Witzke, Mark Stettner, Christoph Kleinschnitz, Alexander Bäuerle, Martin Teufel
{"title":"Respiratory biofeedback and psycho-education for patients with post COVID- 19 symptoms and bodily distress: study protocol of the randomized, controlled explorative intervention trial POSITIV.","authors":"Hannah Dinse, Eva-Maria Skoda, Adam Schweda, Christoph Jansen, Kira Schmidt, Margarethe Konik, Hana Rohn, Oliver Witzke, Mark Stettner, Christoph Kleinschnitz, Alexander Bäuerle, Martin Teufel","doi":"10.1186/s13063-025-08842-6","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>A high number of individuals report suffering from physical and psychological sequelae symptoms after COVID-19-the so-called post COVID-19 condition. Commonly reported complaints include physical symptoms such as fatigue, headache, attention and concentration deficits or dyspnea and anxiety, symptoms of post-traumatic stress, or depression. Evidence-based treatment recommendations are still lacking up to this point. Associations between physical and psychological symptoms in chronic diseases are known for a long time. Support in coping with the disease and improvement of self-efficacy can have a positive effect on the course of diseases. For this reason, we designed a randomized, controlled explorative intervention trial as a treatment of bodily distress disorder in COVID-19 recovered persons.</p><p><strong>Methods: </strong>Patients with a post COVID-19 condition meeting to the criteria of the WHO, along with a bodily distress disorder, are randomized in an intervention and control arm (TAU). Randomization takes place after a diagnostic interview, screening, and informed consent. In total, 60 patients will be included in the trial (30 per group). The intervention group receives a cognitive behavioral therapy as a video-conference-based group therapy (6 weeks) and mobile, respiratory biofeedback treatment (for 4 weeks). At several time points, both groups are assessed in terms of psychological and physical health status, treatment expectation, and satisfaction with the intervention. Furthermore, they will get biofeedback examination appointments. The primary outcome is the change in self-efficacy; secondary outcomes include assessed parameters of mental health, somatic symptoms, and satisfaction with the intervention. Data will be analyzed primarily using R and SPSS.</p><p><strong>Discussion: </strong>The randomized, controlled, explorative intervention trial POSITIV is one of the very first interventions for patients with post COVID-19 condition and psychological burden due to their different symptoms. The aim of the study is to generate new evidence and help patients to cope with the disease and thus, increase their quality of life and reduce symptomatology. We expect with a high probability that the patients' self-efficacy and health status will improve as a result of the intervention.</p><p><strong>Trial registration: </strong>German Clinical Trial Register (DRKS); DRKS-ID: DRKS00030565. Registered on December 22, 2022.</p>","PeriodicalId":23333,"journal":{"name":"Trials","volume":"26 1","pages":"140"},"PeriodicalIF":2.0000,"publicationDate":"2025-04-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12032681/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Trials","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1186/s13063-025-08842-6","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
引用次数: 0

Abstract

Background: A high number of individuals report suffering from physical and psychological sequelae symptoms after COVID-19-the so-called post COVID-19 condition. Commonly reported complaints include physical symptoms such as fatigue, headache, attention and concentration deficits or dyspnea and anxiety, symptoms of post-traumatic stress, or depression. Evidence-based treatment recommendations are still lacking up to this point. Associations between physical and psychological symptoms in chronic diseases are known for a long time. Support in coping with the disease and improvement of self-efficacy can have a positive effect on the course of diseases. For this reason, we designed a randomized, controlled explorative intervention trial as a treatment of bodily distress disorder in COVID-19 recovered persons.

Methods: Patients with a post COVID-19 condition meeting to the criteria of the WHO, along with a bodily distress disorder, are randomized in an intervention and control arm (TAU). Randomization takes place after a diagnostic interview, screening, and informed consent. In total, 60 patients will be included in the trial (30 per group). The intervention group receives a cognitive behavioral therapy as a video-conference-based group therapy (6 weeks) and mobile, respiratory biofeedback treatment (for 4 weeks). At several time points, both groups are assessed in terms of psychological and physical health status, treatment expectation, and satisfaction with the intervention. Furthermore, they will get biofeedback examination appointments. The primary outcome is the change in self-efficacy; secondary outcomes include assessed parameters of mental health, somatic symptoms, and satisfaction with the intervention. Data will be analyzed primarily using R and SPSS.

Discussion: The randomized, controlled, explorative intervention trial POSITIV is one of the very first interventions for patients with post COVID-19 condition and psychological burden due to their different symptoms. The aim of the study is to generate new evidence and help patients to cope with the disease and thus, increase their quality of life and reduce symptomatology. We expect with a high probability that the patients' self-efficacy and health status will improve as a result of the intervention.

Trial registration: German Clinical Trial Register (DRKS); DRKS-ID: DRKS00030565. Registered on December 22, 2022.

COVID- 19后症状和躯体痛苦患者的呼吸生物反馈和心理教育:随机对照探索性干预试验POSITIV的研究方案
背景:大量个体报告在COVID-19后出现身体和心理后遗症症状,即所谓的COVID-19后状态。通常报告的主诉包括身体症状,如疲劳、头痛、注意力和注意力缺陷或呼吸困难和焦虑、创伤后应激症状或抑郁。到目前为止,仍缺乏循证治疗建议。慢性疾病的生理和心理症状之间的联系早已为人所知。在应对疾病和提高自我效能方面的支持可以对疾病的进程产生积极的影响。因此,我们设计了一项随机、对照的探索性干预试验,作为COVID-19康复者身体痛苦障碍的治疗。方法:将符合世卫组织标准的COVID-19后症状并伴有躯体痛苦障碍的患者随机分为干预和对照组(TAU)。随机化在诊断访谈、筛查和知情同意后进行。总共有60名患者将被纳入试验(每组30名)。干预组接受以视频会议为基础的认知行为治疗(6周)和移动呼吸生物反馈治疗(4周)。在几个时间点,对两组患者的心理和身体健康状况、治疗预期和干预满意度进行评估。此外,他们将获得生物反馈检查预约。主要结果是自我效能的改变;次要结局包括心理健康、躯体症状和干预满意度的评估参数。数据将主要使用R和SPSS进行分析。讨论:随机、对照、探索性干预试验POSITIV是针对COVID-19后症状和心理负担患者的首批干预措施之一。这项研究的目的是产生新的证据,帮助患者应对疾病,从而提高他们的生活质量,减少症状。我们很有可能预期患者的自我效能感和健康状况会因干预而改善。试验注册:德国临床试验注册(DRKS);DRKS-ID: DRKS00030565。注册于2022年12月22日。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Trials
Trials 医学-医学:研究与实验
CiteScore
3.80
自引率
4.00%
发文量
966
审稿时长
6 months
期刊介绍: Trials is an open access, peer-reviewed, online journal that will encompass all aspects of the performance and findings of randomized controlled trials. Trials will experiment with, and then refine, innovative approaches to improving communication about trials. We are keen to move beyond publishing traditional trial results articles (although these will be included). We believe this represents an exciting opportunity to advance the science and reporting of trials. Prior to 2006, Trials was published as Current Controlled Trials in Cardiovascular Medicine (CCTCVM). All published CCTCVM articles are available via the Trials website and citations to CCTCVM article URLs will continue to be supported.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信