{"status":"OK","data":{"id":384743,"identifier":"DPAOPC","persistentUrl":"https://doi.org/10.34894/DPAOPC","protocol":"doi","authority":"10.34894","separator":"/","publisher":"DataverseNL","publicationDate":"2023-11-16","storageIdentifier":"surf://10.34894/DPAOPC","effectiveDatasetFileCountLimit":10000,"datasetFileUploadsAvailable":10000,"datasetType":"dataset","locks":[],"latestVersion":{"id":25534,"datasetId":384743,"datasetPersistentId":"doi:10.34894/DPAOPC","datasetType":"dataset","storageIdentifier":"surf://10.34894/DPAOPC","versionNumber":1,"internalVersionNumber":18,"versionMinorNumber":0,"versionState":"RELEASED","latestVersionPublishingState":"RELEASED","deaccessionLink":"","lastUpdateTime":"2023-11-16T11:55:23Z","releaseTime":"2023-11-16T11:55:23Z","createTime":"2023-11-15T10:13:06Z","publicationDate":"2023-11-16","citationDate":"2023-11-16","effectiveDatasetFileCountLimit":10000,"datasetFileUploadsAvailable":10000,"license":{"name":"CC-BY-NC-ND-4.0","uri":"http://creativecommons.org/licenses/by-nc-nd/4.0","iconUri":"https://i.creativecommons.org/l/by-nc-nd/4.0/88x31.png"},"termsOfAccess":"Any request to share the data of this RCT will be considered by the principal investigator and will need to be approved by the ethics committee of the Amsterdam UMC location University of Amsterdam. The meta-dataset is also available at https://COVID19initiatives.health-ri.nl/p/Project/27866022694497984. The informed consent form is published with the protocol paper: https://doi.org/10.1186/s13063-021-05569-y","dataAccessPlace":"The data are stored at Amsterdam UMC.","fileAccessRequest":false,"metadataBlocks":{"citation":{"displayName":"Citation Metadata","name":"citation","fields":[{"typeName":"title","multiple":false,"typeClass":"primitive","value":"ReCOVer: Efficacy of Cognitive-Behavioral Therapy Targeting Severe Fatigue Following Coronavirus Disease 2019"},{"typeName":"alternativeURL","multiple":false,"typeClass":"primitive","value":"https://www.onderzoekmetmensen.nl/en/trial/28363"},{"typeName":"otherId","multiple":true,"typeClass":"compound","value":[{"otherIdAgency":{"typeName":"otherIdAgency","multiple":false,"typeClass":"primitive","value":"https://covid19initiatives.health-ri.nl"},"otherIdValue":{"typeName":"otherIdValue","multiple":false,"typeClass":"primitive","value":"72b56d2f-93b9-402d-a827-e4989d898f77"}}]},{"typeName":"author","multiple":true,"typeClass":"compound","value":[{"authorName":{"typeName":"authorName","multiple":false,"typeClass":"primitive","value":"Knoop, Hans"},"authorAffiliation":{"typeName":"authorAffiliation","multiple":false,"typeClass":"primitive","value":"Amsterdam UMC"},"authorIdentifierScheme":{"typeName":"authorIdentifierScheme","multiple":false,"typeClass":"controlledVocabulary","value":"ORCID"},"authorIdentifier":{"typeName":"authorIdentifier","multiple":false,"typeClass":"primitive","value":"0000-0001-7763-3517"}}]},{"typeName":"datasetContact","multiple":true,"typeClass":"compound","value":[{"datasetContactName":{"typeName":"datasetContactName","multiple":false,"typeClass":"primitive","value":"Knoop, Hans"},"datasetContactAffiliation":{"typeName":"datasetContactAffiliation","multiple":false,"typeClass":"primitive","value":"Amsterdam UMC"}}]},{"typeName":"dsDescription","multiple":true,"typeClass":"compound","value":[{"dsDescriptionValue":{"typeName":"dsDescriptionValue","multiple":false,"typeClass":"primitive","value":"Severe fatigue following coronavirus disease 2019 (COVID-19) is prevalent and debilitating. In the ReCOVer study, the efficacy of cognitive-behavioral therapy (CBT) for severe fatigue following COVID-19 was investigated. This was a multicenter, 2-arm randomized controlled trial conducted in the Netherlands with patients being severely fatigued 3-12 months following COVID-19. Patients were recruited by physicians of 6 participating hospitals in the Netherlands, by healthcare providers, and by self-referral. Patients were assessed for eligibility from November 2020 to September 2021.\n\nPatients (n = 114) were randomly assigned (1:1) to CBT or care as usual (CAU). CBT, targeting perpetuating factors of fatigue, was provided for 17 weeks. The primary outcome was the overall mean difference between CBT and CAU on the fatigue severity subscale of the Checklist Individual Strength, directly post-CBT or CAU (T1), and after 6 months (T2). Secondary outcomes were differences in proportions of patients meeting criteria for severe and/or chronic fatigue, differences in physical and social functioning, somatic symptoms, and problems concentrating between CBT and CAU. For the CBT group, an uncontrolled T3 assessment was administered to measure the treatment effect 1 year after intervention completion.\n\nPatients who received CBT were significantly less severely fatigued across follow-up assessments (T1/T2) compared to patients receiving CAU (Cohen’s d effect size of 0.69).  All secondary outcomes favored CBT. The uncontrolled  long-term follow-up study (T3) revealed that favorable outcomes of CBT were maintained at least up to 1 year post-intervention. \n\nThe dataset entails data of outcomes (see above), cognitive-behavioral factors, actigraphy, personal and demographic characteristics and COVID-19 related variables. See the protocol paper for an overview (Kuut et al., 2021)."}}]},{"typeName":"subject","multiple":true,"typeClass":"controlledVocabulary","value":["Medicine, Health and Life Sciences"]},{"typeName":"keyword","multiple":true,"typeClass":"compound","value":[{"keywordValue":{"typeName":"keywordValue","multiple":false,"typeClass":"primitive","value":"Chronic fatigue, unspecified"},"keywordVocabulary":{"typeName":"keywordVocabulary","multiple":false,"typeClass":"primitive","value":"ICD10: R53.82"}},{"keywordValue":{"typeName":"keywordValue","multiple":false,"typeClass":"primitive","value":"Post COVID-19 condition, unspecified"},"keywordVocabulary":{"typeName":"keywordVocabulary","multiple":false,"typeClass":"primitive","value":"ICD10: U09.9"}},{"keywordValue":{"typeName":"keywordValue","multiple":false,"typeClass":"primitive","value":"Post COVID-19 condition"},"keywordVocabulary":{"typeName":"keywordVocabulary","multiple":false,"typeClass":"primitive","value":"ICD10: U09"}},{"keywordValue":{"typeName":"keywordValue","multiple":false,"typeClass":"primitive","value":"Postviral fatigue syndrome"},"keywordVocabulary":{"typeName":"keywordVocabulary","multiple":false,"typeClass":"primitive","value":"ICD10: G93.31"}},{"keywordValue":{"typeName":"keywordValue","multiple":false,"typeClass":"primitive","value":"Postviral and related fatigue syndromes"},"keywordVocabulary":{"typeName":"keywordVocabulary","multiple":false,"typeClass":"primitive","value":"ICD10: G93.3"}},{"keywordValue":{"typeName":"keywordValue","multiple":false,"typeClass":"primitive","value":"Malaise and fatigue"},"keywordVocabulary":{"typeName":"keywordVocabulary","multiple":false,"typeClass":"primitive","value":"ICD10: R53"}},{"keywordValue":{"typeName":"keywordValue","multiple":false,"typeClass":"primitive","value":"Randomized Controlled Trial [Publication Type]"},"keywordVocabulary":{"typeName":"keywordVocabulary","multiple":false,"typeClass":"primitive","value":"MeSH: D016449"}},{"keywordValue":{"typeName":"keywordValue","multiple":false,"typeClass":"primitive","value":"Cognitive Behavioral Therapy"},"keywordVocabulary":{"typeName":"keywordVocabulary","multiple":false,"typeClass":"primitive","value":"MeSH: D015928"}},{"keywordValue":{"typeName":"keywordValue","multiple":false,"typeClass":"primitive","value":"Post-Acute COVID-19 Syndrome"},"keywordVocabulary":{"typeName":"keywordVocabulary","multiple":false,"typeClass":"primitive","value":"MeSH: D000094024"}},{"keywordValue":{"typeName":"keywordValue","multiple":false,"typeClass":"primitive","value":"COVID-19"},"keywordVocabulary":{"typeName":"keywordVocabulary","multiple":false,"typeClass":"primitive","value":"MeSH: D000086382"}},{"keywordValue":{"typeName":"keywordValue","multiple":false,"typeClass":"primitive","value":"Treatment Outcome"},"keywordVocabulary":{"typeName":"keywordVocabulary","multiple":false,"typeClass":"primitive","value":"MeSH: D016896"}},{"keywordValue":{"typeName":"keywordValue","multiple":false,"typeClass":"primitive","value":"Quality of life"},"keywordVocabulary":{"typeName":"keywordVocabulary","multiple":false,"typeClass":"primitive","value":"MeSH: D011788"}},{"keywordValue":{"typeName":"keywordValue","multiple":false,"typeClass":"primitive","value":"Humans"},"keywordVocabulary":{"typeName":"keywordVocabulary","multiple":false,"typeClass":"primitive","value":"MeSH: D006801"}},{"keywordValue":{"typeName":"keywordValue","multiple":false,"typeClass":"primitive","value":"Netherlands"},"keywordVocabulary":{"typeName":"keywordVocabulary","multiple":false,"typeClass":"primitive","value":"MeSH: D009426"}},{"keywordValue":{"typeName":"keywordValue","multiple":false,"typeClass":"primitive","value":"Multicenter Studies as Topic"},"keywordVocabulary":{"typeName":"keywordVocabulary","multiple":false,"typeClass":"primitive","value":"MeSH: D015337"}},{"keywordValue":{"typeName":"keywordValue","multiple":false,"typeClass":"primitive","value":"Fatigue Syndrome, Chronic"},"keywordVocabulary":{"typeName":"keywordVocabulary","multiple":false,"typeClass":"primitive","value":"MeSH: D015673"}},{"keywordValue":{"typeName":"keywordValue","multiple":false,"typeClass":"primitive","value":"Fatigue"},"keywordVocabulary":{"typeName":"keywordVocabulary","multiple":false,"typeClass":"primitive","value":"MeSH: D005221"}},{"keywordValue":{"typeName":"keywordValue","multiple":false,"typeClass":"primitive","value":"Psychosocial functioning"},"keywordVocabulary":{"typeName":"keywordVocabulary","multiple":false,"typeClass":"primitive","value":"MeSH:  D000083623"}},{"keywordValue":{"typeName":"keywordValue","multiple":false,"typeClass":"primitive","value":"Functional status"},"keywordVocabulary":{"typeName":"keywordVocabulary","multiple":false,"typeClass":"primitive","value":"MeSH: 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A randomised controlled trial testing the efficacy of Fit after COVID, a cognitive behavioural therapy targeting severe post-infectious fatigue following COVID-19 (ReCOVer): study protocol, Trials, 22, 867-681."},"publicationIDType":{"typeName":"publicationIDType","multiple":false,"typeClass":"controlledVocabulary","value":"doi"},"publicationIDNumber":{"typeName":"publicationIDNumber","multiple":false,"typeClass":"primitive","value":"https://doi.org/10.1186/s13063-021-05569-y"},"publicationURL":{"typeName":"publicationURL","multiple":false,"typeClass":"primitive","value":"https://pubmed.ncbi.nlm.nih.gov/34857010/"}},{"publicationCitation":{"typeName":"publicationCitation","multiple":false,"typeClass":"primitive","value":"Kuut, T. A., Müller, F., Csorba, I., Braamse, A., Aldenkamp, A., Appelman, B., Assmann-Schuilwerve, E., Geerlings, S. E., Gibney, K. B., Kanaan, R. A. A., Mooij-Kalverda, K., Olde Hartman, T. C., Pauëlsen, D., Prins, M., Slieker, K., van Vugt, M., Keijmel, S. 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