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Development and content validity of EVAD: A novel tool for evaluating and classifying the severity of adverse events for psychotherapeutic clinical trials
dc.creator | Mejía-Castrejón, Jessica | es_ES |
dc.creator | Sierra-Madero, Juan Gerardo | es_ES |
dc.creator | Belaunzarán-Zamudio, Pablo Francisco | es_ES |
dc.creator | Fresan-Orellana, Ana | es_ES |
dc.creator | Molina-López, Alejandro | es_ES |
dc.creator | Álvarez-Mota, Atenea Betzabé | es_ES |
dc.creator | Robles-García, Rebeca | es_ES |
dc.date | 2024 | |
dc.date.accessioned | 2025-03-10T18:49:51Z | |
dc.date.available | 2025-03-10T18:49:51Z | |
dc.date.issued | 2024 | |
dc.identifier | JC28DIEP23 | es_ES |
dc.identifier.issn | 1050-3307 | |
dc.identifier.uri | http://repositorio.inprf.gob.mx/handle/123456789/8234 | |
dc.identifier.uri | https://doi.org/10.1080/10503307.2023.2239448 | |
dc.description | Objective: Develop and obtain content validity of a new tool for Evaluating and Classifying the Severity of Adverse Events for Psychotherapeutic Clinical Trials (EVAD). Method: Study of the development process of EVAD in four stages: (1) identify the domain and concept definition through a literature review, (2) instrument design, (3) expert judgment of the EVAD items through Gwent's concordance coefficient, and (4) applicability. Results: In the absence of a consistent conceptual framework of adverse events in psychotherapeutic clinical trials, we have developed a framework and defined it. We have designed EVAD items and their complementary tool for rating adverse events. Content validation by expert judges resulted in CVR = 1.0 for each item and CVI = 0.79 in sufficiency, 0.76 in clarity, 0.91 in coherence and 0.95 in relevance for all items (p < 0.001). Final version of EVAD were applied to three participants for 7 weeks. Overall EVAD seems to be clear and meaningful for participants. Conclusions: EVAD is a semistructured interview based on a consistent conceptual framework, and proven content validity following the most important guidelines described in the literature. Trial registration: ClinicalTrials.gov identifier: NCT03878186. | es_ES |
dc.format | es_ES | |
dc.language.iso | eng | es_ES |
dc.publisher | Routledge | es_ES |
dc.relation | 34(4):475-489 | |
dc.rights | Acceso Cerrado | es_ES |
dc.title | Development and content validity of EVAD: A novel tool for evaluating and classifying the severity of adverse events for psychotherapeutic clinical trials | es_ES |
dc.type | Artículo | es_ES |
dc.contributor.affiliation | Medical, Dental and Health Sciences, Universidad Nacional Autónoma de México, Mexico City, Mexico | |
dc.contributor.email | reberobles@imp.edu.mx, reberobles@hotmail.com (Rebeca Robles) | |
dc.relation.jnabreviado | PSYCHOTHER RES | |
dc.relation.journal | Psychotherapy Research | |
dc.identifier.place | Inglaterra | |
dc.date.published | 2024 | |
dc.identifier.organizacion | Instituto Nacional de Psiquiatría Ramón de la Fuente Muñiz | |
dc.identifier.eissn | 1468-4381 | |
dc.identifier.doi | 10.1080/10503307.2023.2239448 | |
dc.subject.kw | Adverse events | |
dc.subject.kw | Evaluation | |
dc.subject.kw | Psychotherapy | |
dc.subject.kw | Clinical trials | |
dc.subject.kw | Patient safety | |
dc.subject.kw | Framework |
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