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NCT06080737 | RECRUITING | SARS-CoV 2 Pneumonia


Long Term Effects of Awake Prone Positioning in COVID-19 ICU Patients
Sponsor:

University Hospital, Tours

Brief Summary:

Long term follow up of patients included in a randomized controlled trial evaluating awake prone positioning among patients suffering SARS-CoV2 pneumonia (NCT04358939)

Condition or disease

SARS-CoV 2 Pneumonia

Intervention/treatment

quality of life questionnaire

Detailed Description:

All patients included in the initial trial who survived and were not lost to follow up at 28 days will be invited for a telephone interview to collect data on long term quality of life.

Study Type : OBSERVATIONAL
Estimated Enrollment : 300 participants
Official Title : Effects of Awake Prone Positioning on Long-term Quality of Life in Patients Managed in the ICU Under Nasal High Flow for SARS-CoV2 Pneumonia, a Cohort Study Nested Within a Randomized Trial
Actual Study Start Date : 2024-05-03
Estimated Primary Completion Date : 2025-12
Estimated Study Completion Date : 2025-12

Information not available for Arms and Intervention/treatment

Ages Eligible for Study: 18 Years
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers:
Criteria
Inclusion Criteria
  • * Patients included in the randomized meta-trial evaluating awake prone position versus control among COVID-19 patients on high-flow nasal oxygen therapy (Ehrmann 2021).
  • * Patients alive at D28
  • * No opposition to participate in the research which evaluates mortality and quality of life by telephone interview.
Exclusion Criteria
  • * Patients lost to follow-up after 28 days.
  • * Withdrawal of consent from randomized meta-trial by patient
  • * Vulnerable person: safeguard of justice, curatorship, or guardianship
  • * Patients refusing to answer telephone questionnaire.

Long Term Effects of Awake Prone Positioning in COVID-19 ICU Patients

Location Details

NCT06080737


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How to Participate

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Locations


RECRUITING

France,

university hospital Tours

Tours, France, 37000

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