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1.
Contemp Clin Trials ; 111: 106619, 2021 12.
Article in English | MEDLINE | ID: covidwho-1574060

ABSTRACT

Characterizing the impacts of disruption attributable to the COVID-19 pandemic on clinical research is important, especially in pain research where psychological, social, and economic stressors attributable to the COVID-19 pandemic may greatly impact treatment effects. The National Institutes of Health - Department of Defense - Department of Veterans Affairs Pain Management Collaboratory (PMC) is a collective effort supporting 11 pragmatic clinical trials studying nonpharmacological approaches and innovative integrated care models for pain management in veteran and military health systems. The PMC rapidly developed a brief pandemic impacts measure for use across its pragmatic trials studying pain while remaining broadly applicable to other areas of clinical research. Through open discussion and consensus building by the PMC's Phenotypes and Outcomes Work Group, the PMC Coronavirus Pandemic (COVID-19) Measure was iteratively developed. The measure assesses the following domains (one item/domain): access to healthcare, social support, finances, ability to meet basic needs, and mental or emotional health. Two additional items assess infection status (personal and household) and hospitalization. The measure uses structured responses with a three-point scale for COVID-19 infection status and four-point ordinal rank response for all other domains. We recommend individualized adaptation as appropriate by clinical research teams using this measure to survey the effects of the COVID-19 pandemic on study participants. This can also help maintain utility of the measure beyond the COVID-19 pandemic to characterize impacts during future public health emergencies that may require mitigation strategies such as periods of quarantine and isolation.


Subject(s)
COVID-19 , Pragmatic Clinical Trials as Topic , Humans , Pandemics , Quarantine , Social Support , United States/epidemiology
2.
Mil Med ; 187(7-8): 179-185, 2022 07 01.
Article in English | MEDLINE | ID: covidwho-1522250

ABSTRACT

Pragmatic clinical trials (PCTs) are well-suited to address unmet healthcare needs, such as those arising from the dual public health crises of chronic pain and opioid misuse, recently exacerbated by the COVID-19 pandemic. These overlapping epidemics have complex, multifactorial etiologies, and PCTs can be used to investigate the effectiveness of integrated therapies that are currently available but underused. Yet individual pragmatic studies can be limited in their reach because of existing structural and cultural barriers to dissemination and implementation. The National Institutes of Health, Department of Defense, and Department of Veterans Affairs formed an interagency research partnership, the Pain Management Collaboratory. The partnership combines pragmatic trial design with collaborative tools and relationship building within a large network to advance the science and impact of nonpharmacological approaches and integrated models of care for the management of pain and common co-occurring conditions. The Pain Management Collaboratory team supports 11 large-scale, multisite PCTs in veteran and military health systems with a focus on team science with the shared aim that the "whole is greater than the sum of the parts." Herein, we describe this integrated approach and lessons learned, including incentivizing all parties; proactively offering frequent opportunities for problem-solving; engaging stakeholders during all stages of research; and navigating competing research priorities. We also articulate several specific strategies and their practical implications for advancing pain management in active clinical, "real-world," settings.


Subject(s)
Military Personnel , Pragmatic Clinical Trials as Topic , Veterans , COVID-19 , Humans , Pain Management , Pandemics , Research Design
4.
J Am Geriatr Soc ; 69(10): 2741-2744, 2021 10.
Article in English | MEDLINE | ID: covidwho-1262362

ABSTRACT

BACKGROUND: Because of the COVID-19 pandemic, the ongoing D-CARE pragmatic trial of two models of dementia care management needed to transition to all data collection by telephone. METHODS: For the first 1069 D-CARE participants, we determined the feasibility of administering a short 3-item version of the Montreal Cognitive Assessment (MoCA) to persons with dementia by telephone and examined the correlation with the full 12-item version. RESULTS: The 3-item version could be administered by telephone in approximately 6 min and was highly correlated with the full MoCA (r = 0.78, p < 0.0001). CONCLUSIONS: This brief version of the MoCA was feasible to collect by telephone and could be used as an alternative to the full MoCA, particularly if the purpose of cognitive assessment is characterization of study participants.


Subject(s)
COVID-19 , Dementia , Mental Status and Dementia Tests , Patient Care Management , Telemedicine/methods , Aged , Aged, 80 and over , COVID-19/epidemiology , COVID-19/prevention & control , Cognitive Dysfunction/diagnosis , Dementia/diagnosis , Dementia/psychology , Dementia/therapy , Female , Humans , Infection Control/methods , Interviews as Topic/methods , Male , Patient Care Management/methods , Patient Care Management/trends , Reproducibility of Results , SARS-CoV-2
5.
Transl Behav Med ; 10(4): 827-834, 2020 10 08.
Article in English | MEDLINE | ID: covidwho-744584

ABSTRACT

The COVID-19 pandemic has slowed research progress, with particularly disruptive effects on investigations of addressing urgent public health challenges, such as chronic pain. The National Institutes of Health (NIH) Department of Defense (DoD) Department of Veterans Affairs (VA) Pain Management Collaboratory (PMC) supports 11 large-scale, multisite, embedded pragmatic clinical trials (PCTs) in military and veteran health systems. The PMC rapidly developed and enacted a plan to address key issues in response to the COVID-19 pandemic. The PMC tracked and collaborated in developing plans for addressing COVID-19 impacts across multiple domains and characterized the impact of COVID-19 on PCT operations, including delays in recruitment and revisions of study protocols. A harmonized participant questionnaire will facilitate later meta-analyses and cross-study comparisons of the impact of COVID-19 across all 11 PCTs. The pandemic has affected intervention delivery, outcomes, regulatory and ethics issues, participant recruitment, and study design. The PMC took concrete steps to ensure scientific rigor while encouraging flexibility in the PCTs, while paying close attention to minimizing the burden on research participants, investigators, and clinical care teams. Sudden changes in the delivery of pain management interventions will probably alter treatment effects measured via PMC PCTs. Through the use of harmonized instruments and surveys, we are capturing these changes and plan to monitor the impact on research practices, as well as on health outcomes. Analyses of patient-reported measures over time will inform potential relationships between chronic pain, mental health, and various socioeconomic stressors common among Americans during the COVID-19 pandemic.


Subject(s)
Communicable Disease Control/methods , Coronavirus Infections , Mental Health/trends , Pain Management , Pandemics , Pneumonia, Viral , Research , Betacoronavirus , COVID-19 , Chronic Pain/epidemiology , Chronic Pain/psychology , Chronic Pain/therapy , Coronavirus Infections/epidemiology , Coronavirus Infections/prevention & control , Humans , National Institutes of Health (U.S.) , Pain Management/ethics , Pain Management/methods , Pain Management/trends , Pandemics/prevention & control , Patient Selection , Pneumonia, Viral/epidemiology , Pneumonia, Viral/prevention & control , Research/organization & administration , Research/trends , SARS-CoV-2 , Socioeconomic Factors , United States/epidemiology , United States Department of Veterans Affairs
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