COVID19-OR (SARS-CoV-2): Observation,Risk & Recovery

Sponsor
Western Sussex Hospitals NHS Trust (Other)
Overall Status
Completed
CT.gov ID
NCT04524520
Collaborator
(none)
194
1
25.1
7.7

Study Details

Study Description

Brief Summary

A novel coronavirus, designated corona virus disease 2019 (COVID-19) has resulted in a Pandemic at the time of writing (27th April) the reported number of confirmed cases exceeding 3 million and over 200000 associated deaths.

The burden on global critical care has been considerable. As of 24th April there have been 8752 UK critical care admissions with services under considerable strain, and a mortality rate over 50%. Survivors of critical illness will require significant input.

This study will perform mixed methods to provide rich data on risk stratification and recovery from critical illness. Recovery from a novel disease requires documenting and the study reports physical and psychological changes following hospital discharge in survivors. In addition qualitative interviews are being conducted with patients who have survived and been discharged from critical care along with their relatives and treating professionals, to better understand their needs during recovery.

Study Design

Study Type:
Observational
Actual Enrollment :
194 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
COVID19-OR (SARS-CoV-2):Observation, Risk & Recovery. An Observational Study Exploring Risk Assessment and Recovery From COVID-19 (SARS-CoV-2) Infection in Hospitalised Patients
Actual Study Start Date :
May 5, 2020
Actual Primary Completion Date :
May 8, 2022
Actual Study Completion Date :
Jun 8, 2022

Outcome Measures

Primary Outcome Measures

  1. Physical [through study completion , an average of 1 year]

    Chelsea critical care physical assessment tool

  2. Physical [through study completion , an average of 1 year]

    Incremental Shuttle Walk Test (ISWT)

  3. Physical [through study completion , an average of 1 year]

    1- minute Sit to Stand, Grip strength

  4. Health Related Quality of life [at 3 months]

    Short Form Survey on health related quality of life (SF-12). Two summary scores are reported from the SF-12 - a mental component score (MCS-12) and a physical component score (PCS-12). The scores may be reported as Z-scores (difference compared to the population average, measured in standard deviations). The United States population average PCS-12 and MCS-12 are both 50 points. Higher scores indicate better outcome.

  5. Health Related Quality of life [at 1 year]

    Short Form Survey on health related quality of life (SF-36). Scores can range from 0 to 100 and a higher score indicates better outcome.

  6. Psychological [through study completion , an average of 1 year]

    Depression Test Questionnaire (PHQ-9). Scores range from 1 to 27 and higher scores indicate worse outcome.

  7. Psychological [through study completion , an average of 1 year]

    Anxiety Test Questionnaire (GAD-7). Scores range from 0 to 21 and higher scores indicates worse outcome.

  8. Psychological [through study completion , an average of 1 year]

    Montreal Cognitive Assessment (MoCA). Scores range from 0 to 30 and higher scores indicate a better outcome.

  9. Psychological [at 1 year]

    Post-traumatic stress disorder (PTSD) Trauma Screening (TSQ). A screening tool with 10 items. If 6 items are endorsed then the outcome is 'positive' for PTSD.

Secondary Outcome Measures

  1. risk stratification [through study completion and average of 1 year]

    escalation to critical care (Yes/No)

  2. risk stratification [through study completion and average of 1 year]

    mechanical ventilation (Yes/No)

  3. risk stratification [through study completion and average of 1 year]

    critical care stay hospital stay (number of days)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Adults ≥18 years admitted to ICU with SARS-CoV-2 and survived

  2. Relatives or friends and professionals involved in the care of these patients.

Exclusion Criteria:
  1. Patients <18 years;

  2. Patients with a negative test for SARS-CoV-2 or patients not tested due to absence of symptoms;

Contacts and Locations

Locations

Site City State Country Postal Code
1 Dr Luke Hodgson Worthing United Kingdom

Sponsors and Collaborators

  • Western Sussex Hospitals NHS Trust

Investigators

  • Principal Investigator: Dr Luke Hodgson, Western Sussex Hospitals NHS Trust

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Western Sussex Hospitals NHS Trust
ClinicalTrials.gov Identifier:
NCT04524520
Other Study ID Numbers:
  • 20/YH/0157
First Posted:
Aug 24, 2020
Last Update Posted:
Jul 18, 2022
Last Verified:
Jul 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 18, 2022