Rapid evaluation of the COVID-19 pandemic response in palliative and end of life care: national delivery, workforce and symptom management (CovPall)

  • Funded by Department of Health and Social Care / National Institute for Health and Care Research (DHSC-NIHR), UK Research and Innovation (UKRI)
  • Total publications:35 publications

Grant number: MR/V012908/1

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Key facts

  • Disease

    COVID-19
  • Start & end year

    2020
    2021
  • Known Financial Commitments (USD)

    $172,361.6
  • Funder

    Department of Health and Social Care / National Institute for Health and Care Research (DHSC-NIHR), UK Research and Innovation (UKRI)
  • Principal Investigator

    Prof. Irene Higginson
  • Research Location

    United Kingdom
  • Lead Research Institution

    King's College London
  • Research Priority Alignment

    N/A
  • Research Category

    Clinical characterisation and management

  • Research Subcategory

    Disease pathogenesis

  • Special Interest Tags

    N/A

  • Study Type

    Clinical

  • Clinical Trial Details

    Not applicable

  • Broad Policy Alignment

    Pending

  • Age Group

    Unspecified

  • Vulnerable Population

    Unspecified

  • Occupations of Interest

    Unspecified

Abstract

The COVID-19 pandemic is placing an unprecedented strain on health care services. Although many people survive, an estimated 1 to 4% die from this disease. There are more than 10,000 UK deaths from COVID-19, with numbers escalating. Many of the symptoms, such as breathlessness, fever, agitation and pain, are very distressing. But in this new disease these symptoms are not well understood. Palliative care services are adapting rapidly to this situation, but in different ways, not knowing what is best. This research aims to rapidly evaluate the palliative care response in COVID-19 to improve care now and in the future. There are two main components, called work packages (WPs), to the research. WP1 surveys, UK wide, palliative care medical or nursing leads, about their changes in practice, how they deploy the workforce, volunteers and technology, their innovations and challenges. WP2 collects data about patients' symptoms, how they change over time, and the effects of treatments. We collect this information immediately and quickly (phase I), and then repeat the data collection after 6-8 weeks (phase II) to understand how practice is changing. We involve patients, families, the public, policy makers and services in all stages of the research. We release early findings, to help catalyse an effective response.

Publicationslinked via Europe PMC

Last Updated:14 hours ago

View all publications at Europe PMC

Prevalence and demographics of 331 rare diseases and associated COVID-19-related mortality among 58 million individuals: a nationwide retrospective observational study.

Practice review: Pharmacological management of severe chronic breathlessness in adults with advanced life-limiting diseases.

Telephone advice lines for adults with advanced illness and their family carers: a qualitative analysis and novel practical framework.

General practice service use at the end-of-life before and during the COVID-19 pandemic: a population-based cohort study using primary care electronic health records.

Adaptation and multicentre validation of a patient-centred outcome scale for people severely ill with COVID (IPOS-COV).

The Six-minute Step Test as an Exercise Outcome in Chronic Obstructive Pulmonary Disease.

Top Ten Tips Palliative Care Clinicians Should Know About Cachexia.

Update on the Etiology, Assessment, and Management of COPD Cachexia: Considerations for the Clinician.

Correction: Charitably funded hospices and the challenges associated with the COVID-19 pandemic: a mixed-methods study (CovPall).