Dine Jennifer, Guan Yanfen, Milien Mirline, Ervin Claire, Byrne Dana D, Brown Michelle L, De Anda Carisa, Norquist Josephine M
RTI Health Solutions, Research Triangle Park, Durham, NC, USA.
Merck & Co., Inc., Rahway, NJ, USA.
Patient Relat Outcome Meas. 2025 Jan 17;16:37-53. doi: 10.2147/PROM.S488914. eCollection 2025.
The COVID-19 Symptoms Daily Diary (CSDD) is a patient-reported outcome measure designed to assess the severity of core COVID-19 symptoms in clinical trials. The preliminary version of the CSDD was developed based on regulatory guidance and the hallmark COVID-19 symptoms identified by the CDC. This study aimed to evaluate CSDD content validity, to determine whether it is fit for the purpose of supporting efficacy endpoints in clinical trials of treatments for COVID-19. This research also sought to evaluate the appropriateness of a newly developed Pre-COVID-19 Symptoms Questionnaire.
A targeted literature review was completed to evaluate the relevance of concepts included in the diary and to identify any important symptoms that may have been missing. Hybrid (concept elicitation and cognitive debriefing) semistructured qualitative interviews were then conducted across 3 iterative rounds with 30 adults in the United States recently diagnosed with COVID-19.
The CSDD included concepts that were most frequently reported by interview participants, including those identified as most bothersome and most important to treat. During cognitive debriefing, participants described the diary concepts as salient and reported the instructions, recall period, and response options as clear and appropriate. Only 2 of 15 CSDD items were modified across 3 interview rounds; specifically, definitions for the vomiting and diarrhea frequency items were clarified for consistent interpretation and response. Interview participants also reported general ease in understanding and responding to the Pre-COVID-19 questionnaire, with feedback resulting in only minor changes to the reference period and instructions.
The findings of the current study provide strong evidence for the content validity of the CSDD and the appropriateness of each of the items assessed. This rigorous evaluation (aligned with regulatory guidance) indicates that the CSDD is fit for the purpose of supporting efficacy endpoints in planned clinical trials evaluating medications for COVID-19 treatment.
COVID-19症状每日日记(CSDD)是一种患者报告的结局指标,旨在评估临床试验中COVID-19核心症状的严重程度。CSDD的初步版本是根据监管指南和美国疾病控制与预防中心(CDC)确定的COVID-19标志性症状制定的。本研究旨在评估CSDD的内容效度,以确定其是否适合用于支持COVID-19治疗临床试验中的疗效终点。本研究还试图评估新开发的COVID-19前症状问卷的适用性。
完成了一项有针对性的文献综述,以评估日记中所包含概念的相关性,并识别可能遗漏的任何重要症状。随后,对30名最近在美国被诊断为COVID-19的成年人进行了三轮混合(概念引出和认知反馈)半结构化定性访谈。
CSDD包含了访谈参与者最常报告的概念,包括那些被认为最困扰且最需要治疗的概念。在认知反馈过程中,参与者将日记中的概念描述为显著的,并表示说明、回忆期和回答选项清晰且恰当。在三轮访谈中,15项CSDD条目仅修改了2项;具体而言,对呕吐和腹泻频率条目的定义进行了澄清,以便进行一致的解释和回答。访谈参与者还报告说,理解和回答COVID-19前问卷总体较为轻松,反馈结果仅对参考期和说明进行了微小修改。
本研究结果为CSDD的内容效度以及所评估的每个条目的适用性提供了有力证据。这种严格的评估(符合监管指南)表明,CSDD适合用于支持评估COVID-19治疗药物的计划临床试验中的疗效终点。