Research lessons during the COVID-19 pandemic: collecting longitudinal physical and mental health outcomes

Author:

Grove KristenORCID,Harrold Megan,Mohd Sheeraz,Natarajan Varsha,Hurn Elizabeth,Pearce Jane,Cavalheri Vinicius,Watson Carol,Edgar Dale W.,Maiorana Andrew,Jacques Angela,White Ann,Vicary Caitlin,Watson Carol,Roffman Caroline,Synnott Emma-Leigh,Chih Hui Jun,Suttie Ian,Lin Ivan,Larsson Jade,Tearne Jessica,Woodhouse Linda,van der Lee Lisa,Naylor Louise,Elliott Mercedes,Gittings Paul,Winship Peta,Timms Robyn,Wulff Sheldon,Hebden-Todd Tracy,

Abstract

Abstract Background Participant enrolment, assessment and/or delivery of intervention in many clinical trials during the COVID-19 pandemic were severely impacted by public health measures limiting physical contact. This report describes the lessons learned in completing a repeated measures cohort study involving suspected and confirmed COVID-19 survivors at three sites in Perth, Western Australia. Main body An observational analysis of the conduct and data completeness results of the LATER-19 trial. People with COVID19 symptoms who were tested between February and November 2020 were recruited. In both those who tested positive and those who tested negative (control group) for COVID19, data on physical function and mental health were collected at two time points up to eight months after COVID19 testing. Recruitment of the controls was targeted from hospital records for comparison, it was balanced for age and sex and for the non-hospitalised group also comorbidities. A sample of 344 participants was recruited: 155 (45.1%) COVID-19 positive. Taking the research design and environmental adaptations into account, we recorded > 90% participant engagement during the trial. Of the 637 planned assessments, objective measures were completed on 602 (94.5%) occasions; 543 (90.2%) were on-site and 59 (9.8%) were remote. A total of 577 (90.6%) mental health/symptoms surveys, 569 (89.3%) 1-min sit-to-stand tests, and 520 (81.6%) handgrip strength tests were completed. Conclusion The sample size and high completion rate of planned assessments during the LATER-19 trial potentially increases the contextual, groupwise generalisability of the results. The results demonstrate the effectiveness of a simple, rapid, reproducible and adaptable battery of assessments, leveraging telehealth and digital solutions. Trial registration number Australian and New Zealand Clinical Trial Registration (ANZCTR): ACTRN12621001067864.

Funder

Western Australian Health Translation Network

Publisher

Springer Science and Business Media LLC

Subject

Public Health, Environmental and Occupational Health

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