Rehabilitation for People With COVID-19 in ICU : Pulmonary and Motor Rehabilitation for People With COVID-19 in Intensive Care Units to Reduce Length of Stay in Hospital

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 InterventionRehabilitation 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/balanceMotor programIntubated patient Glasgow Coma Scale (GCS) >8: passive mobilisation; postural positioning Glasgow Coma Scale < 8 (weaning): passive and active-assist mobilisation; postural positioningWeaned off patient Non-invasively ventilated/O2 high fluxesIf strength < 3 MRC: passive and/or active-assist; tentative functional retrainingIf strength ≥3 MRC: active-assist and active; strength training; functional retraining Pulmonary RehabilitationIntubated patient Glasgow Coma Scale >8: postural positioning Glasgow Coma Scale < 8 (weaning): postural positioning, cautious inspiratory muscle trainingWeaned off patient Non-invasively ventilated/O2 high fluxesIf strength < 3 MRC: postural positioning, positive pressure expiration exercise, cautious inspiratory muscle trainingIf strength ≥3 MRC: postural positioning, positive pressure expiration exercise, inspiratory muscle trainingThe 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 retrainingrespiratory rehabilitation Frequency of sessions: 3×15 min/day.

Medienart:	Klinische Studie

Erscheinungsjahr:	2023
Erschienen:	2023

Enthalten in:	ClinicalTrials.gov - (2023) vom: 18. Nov. Zur Gesamtaufnahme - year:2023

Sprache:	Englisch

Links:	Volltext [kostenfrei]

Themen:	610 Acute Lung Injury COVID-19 Coronavirus Infections Critical Illness Lung Injury Recruitment Status: Completed Respiratory Distress Syndrome Respiratory Distress Syndrome, Newborn Study Type: Interventional Virus Diseases

Anmerkungen:	Source: Link to the current ClinicalTrials.gov record., First posted: May 8, 2020, Last downloaded: ClinicalTrials.gov processed this data on November 22, 2023, Last updated: November 22, 2023

Study ID:

NCT04381338 UPadova_1

Veröffentlichungen zur Studie:

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PPN (Katalog-ID):	CTG003386406