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Rehabilitation for People With COVID-19 in ICU (COVID_REHAB)

Primary Purpose

Corona Virus Disease 19 (COVID-19), COVID, Acute Lung Injury/Acute Respiratory Distress Syndrome (ARDS)

Status
Unknown status
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Pulmonary and Motor Rehabilitation
Sponsored by
University of Padova
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Corona Virus Disease 19 (COVID-19) focused on measuring Recovery, Outcome, retraining, corona virus disease 19

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Confirmed COVID-19 diagnosis, admitted to ICU with ARDS

Exclusion Criteria:

  • Neuromuscular disease, severe heart failure (class IV), persistent severe hypotension (systolic BP < 90mmHg), disorder of consciousness (DoC)

Sites / Locations

  • Teaching Hospital, University of Padova
  • Teaching Hospital, University of Verona

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Rehabilitation in COVID-19 patients in ICU

COVID-19 in ICU without Rehabilitation

Arm Description

Every person admitted to ICU for ARDS with a confirmed diagnosis of COVID-19 Motor program Intubated patient GCS >8: passive mobilization; postural positioning GCS< 8: passive and active-assist mobilization; postural positioning Extubated patient If strength < 3 MRC: passive and/or active-assist; functional retraining If strength ≥3 MRC: active-assist and active; strength training; functional retraining Pulmonary Rehabilitation Intubated patient GCS >8: postural positioning GCS< 8: postural positioning, cautious inspiratory muscle training Extubated patient If strength < 3 MRC: postural positioning, positive pressure expiration exercise,inspiratory muscle training If strength ≥3 MRC: postural positioning, positive pressure expiration exercise, inspiratory muscle training The intensity of exercise will prescribed based on the results of the PFIT. and modified Borg Scale. Frequency of sessions: 3×15 min/day

Standard of care without rehabilitation in ICU

Outcomes

Primary Outcome Measures

Length of ICU stay
days of ICU stay

Secondary Outcome Measures

Length of hospital stay
days of hospital stay

Full Information

First Posted
May 4, 2020
Last Updated
May 7, 2020
Sponsor
University of Padova
Collaborators
Prof. S Masiero, University of Padova, Italy, Dr. A. Venturin, General Hosipital, Padova, Italy, Dr. I. Tiberio, General Hospital, Padova, Italy, Dr. D. Zampieri, University of Padova, Italy, Dr.ssa M Cattelan, University of Padova, Italy, Prof. P. Zanatta, University Hosiptal, Verona, Italy, Dr.ssa C. Carollo, General Hospital, Padova, Italy, Prof. E. Polati, University Hospital, Verona, Italy, Prof. K. Donadello, University Hospital, Verona, Italy
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1. Study Identification

Unique Protocol Identification Number
NCT04381338
Brief Title
Rehabilitation for People With COVID-19 in ICU
Acronym
COVID_REHAB
Official Title
Pulmonary and Motor Rehabilitation for People With COVID-19 in Intensive Care Units to Reduce Length of Stay in Hospital
Study Type
Interventional

2. Study Status

Record Verification Date
May 2020
Overall Recruitment Status
Unknown status
Study Start Date
May 10, 2020 (Anticipated)
Primary Completion Date
September 30, 2020 (Anticipated)
Study Completion Date
September 30, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Padova
Collaborators
Prof. S Masiero, University of Padova, Italy, Dr. A. Venturin, General Hosipital, Padova, Italy, Dr. I. Tiberio, General Hospital, Padova, Italy, Dr. D. Zampieri, University of Padova, Italy, Dr.ssa M Cattelan, University of Padova, Italy, Prof. P. Zanatta, University Hosiptal, Verona, Italy, Dr.ssa C. Carollo, General Hospital, Padova, Italy, Prof. E. Polati, University Hospital, Verona, Italy, Prof. K. Donadello, University Hospital, Verona, Italy

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
COVID-19 DISEASE Coronavirus disease 2019 (COVID-19) is a respiratory tract infection caused by a newly emergent coronavirus, severe acute respiratory syndrome from COVID-19, that was first recognized in Wuhan, China, in December 2019. While most people with COVID-19 develop mild or uncomplicated illness, approximately 14% develop severe disease requiring hospitalization and oxygen support and 5% require admission to an intensive care unit. In severe cases, COVID-19 can be complicated by acute respiratory disease syndrome (ARDS) requiring prolonged mechanical ventilation, sepsis and septic shock, multiorgan failure, including acute kidney, liver and cardiac injury. ARDS REHABILITATION Critically ill people who undergo prolonged mechanical ventilation often develop weakness, with severe symmetrical weakness of and deconditioning of the proximal musculature and of the respiratory muscles (critical illness neuropathy/myopathy).These individuals also develop significant functional impairment and reduced health-related quality of life (HRQL) up to 2 and 5 years after discharge. ARDS survivors may complain of depression, anxiety, memory disturbances, and difficulty with concentration often unchanged at 2 and 5 years. Less than half of all ARDS survivors return to work within the first year following discharge, two-thirds at two years, and more than 70% at five years. Early physiotherapy (PT) of people with ARDS has recently been suggested as a complementary therapeutic tool to improve early and late outcomes. The aims of PT programs should be to reduce complications of immobilization and ventilator-dependency, to improve residual function, to prevent new hospitalisations, and to improve health status and HRQL. Physiotherapy in critical patients is claimed also to prevent and contribute to treat respiratory complications such as secretion retention, atelectasis, and pneumonia. Early mobilization and maintenance of muscle strength may reduce the risk of difficult weaning, limited mobility, and ventilator dependency. Lastly, pulmonary rehabilitation in ICU in mechanically ventilated subjects may reduce length of stay in ICU up to 4.5 day, shorten mechanical ventilation of 2.3 days and weaning by 1.7 days. The aim of this study is to investigate how early pulmonary and motor rehabilitation impacts on length of hospital admission (ICU and acute ward) and early and late outcomes inpatients that develop ARDS due to COVID-19.
Detailed Description
People that develop ARDS due to COVID-19 and requiring admission to ICU (both invasive and non-invasive mechanical ventilation) will be enrolled. Two tertiary referral centers, part of the same region (Veneto) but located in different cities, will recruit participants. ICU standard of care is the same as defined by regional and national guidelines; rehabilitation in ICU COVID-19 subjects is provided only in one center due to local technical and organizational limitations. Non contamination between centers is possible due to restrictions of mobility and strict admission criteria based on catchment area. Early physiotherapy treatment will start from the day of admission. Baseline measurement of physical function will performed using the Physical Function in ICU Test (PFIT). The PFIT is a submaximal exercise test that was developed for patients in the ICU who may not be able to mobilize away from the bedside. Participants will start rehabilitation if they will not experiment one of the following conditions or should cease exercise because of the following (see exclusion criteria). Rehabilitation Intervention Rehabilitation program will start at admission in ICU. The program is based on the clinical characteristics of the individual to be treated. Participants will commence a hierarchical, standardized protocol that includes functional, respiratory and strength training. If participants will be unable to sit out of bed, assisted active exercises will be performed in bed. Exercise training will be provided for 15 minutes 3 times/day, 6 days per week. Intensity of strength training: Until fatigue (Borg Scale) Type of strength training: >Grade 3 Medical Research Council (MRC) strength, active to resisted; <Grade 3 MRC strength, active assist to active Repetitions for strength training: Start 5 repetitions each limb, Progress to 3 sets of 10 repetitions as able Functional retraining: Sit-to-stand (using tilt table or standing walker if unable), rolling, supine to sitting, trunk control/balance Motor program Intubated patient Glasgow Coma Scale (GCS) >8: passive mobilisation; postural positioning Glasgow Coma Scale < 8 (weaning): passive and active-assist mobilisation; postural positioning Weaned off patient Non-invasively ventilated/O2 high fluxes If strength < 3 MRC: passive and/or active-assist; tentative functional retraining If strength ≥3 MRC: active-assist and active; strength training; functional retraining Pulmonary Rehabilitation Intubated patient Glasgow Coma Scale >8: postural positioning Glasgow Coma Scale < 8 (weaning): postural positioning, cautious inspiratory muscle training Weaned off patient Non-invasively ventilated/O2 high fluxes If strength < 3 MRC: postural positioning, positive pressure expiration exercise, cautious inspiratory muscle training If strength ≥3 MRC: postural positioning, positive pressure expiration exercise, inspiratory muscle training The intensity of exercise will prescribed based on the results of the PFIT. Rehabilitation programs will individualized for each patient. Programs will progressed using rates of perceived exertion (RPE) of the modified Borg Scale. Total session time composition:15 min to complete: Whole-body bed exercises + strength + functional retraining respiratory rehabilitation Frequency of sessions: 3×15 min/day

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Corona Virus Disease 19 (COVID-19), COVID, Acute Lung Injury/Acute Respiratory Distress Syndrome (ARDS), Critical Illness
Keywords
Recovery, Outcome, retraining, corona virus disease 19

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Clustered, due to catchment area of Hospital with no chance of contamination because of lock down in the area.
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
92 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Rehabilitation in COVID-19 patients in ICU
Arm Type
Experimental
Arm Description
Every person admitted to ICU for ARDS with a confirmed diagnosis of COVID-19 Motor program Intubated patient GCS >8: passive mobilization; postural positioning GCS< 8: passive and active-assist mobilization; postural positioning Extubated patient If strength < 3 MRC: passive and/or active-assist; functional retraining If strength ≥3 MRC: active-assist and active; strength training; functional retraining Pulmonary Rehabilitation Intubated patient GCS >8: postural positioning GCS< 8: postural positioning, cautious inspiratory muscle training Extubated patient If strength < 3 MRC: postural positioning, positive pressure expiration exercise,inspiratory muscle training If strength ≥3 MRC: postural positioning, positive pressure expiration exercise, inspiratory muscle training The intensity of exercise will prescribed based on the results of the PFIT. and modified Borg Scale. Frequency of sessions: 3×15 min/day
Arm Title
COVID-19 in ICU without Rehabilitation
Arm Type
No Intervention
Arm Description
Standard of care without rehabilitation in ICU
Intervention Type
Other
Intervention Name(s)
Pulmonary and Motor Rehabilitation
Intervention Description
Pulmonary and Motor Rehabilitation in ICU
Primary Outcome Measure Information:
Title
Length of ICU stay
Description
days of ICU stay
Time Frame
up to 60 days
Secondary Outcome Measure Information:
Title
Length of hospital stay
Description
days of hospital stay
Time Frame
up to 90 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Confirmed COVID-19 diagnosis, admitted to ICU with ARDS Exclusion Criteria: Neuromuscular disease, severe heart failure (class IV), persistent severe hypotension (systolic BP &lt; 90mmHg), disorder of consciousness (DoC)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Alessandra Del Felice, MD, PhD
Phone
+39-0498212598
Email
alessandra.delfelice@unipd.it
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alessandra Del Felice, MD, PhD
Organizational Affiliation
University of Padova
Official's Role
Principal Investigator
Facility Information:
Facility Name
Teaching Hospital, University of Padova
City
Padova
Country
Italy
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Alessandra Del Felice, MD, PhD
Phone
0039(0)498211270
Email
alessandra.delfelice@unipd.it
Facility Name
Teaching Hospital, University of Verona
City
Verona
ZIP/Postal Code
37126
Country
Italy
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Katia Donadello, MD, PhD
Email
katia.donadello@univr.it

12. IPD Sharing Statement

Plan to Share IPD
No
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Rehabilitation for People With COVID-19 in ICU

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