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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05865314
Other study ID # NutriPhyT2022
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date May 2023
Est. completion date September 2024

Study information

Verified date May 2023
Source University Hospital, Geneva
Contact Claudia Heidegger, MD
Phone + 41 22 37 27 440
Email claudia.heidegger@hcuge.ch
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Due to medical advances and quality of care, mortality in adult intensive care units (ICUs) has decreased significantly in recent years, leading to a significant increase in the number of patients with high rehabilitation needs on discharge from the ICU. A specific management by a multidisciplinary team has been set up since 2017 at the Geneva-ICU for long-stay patients (hospitalised ≥ 7 days). This study aim to assess whether an optimization of the nutritional therapy coupled with an early mobility during and after the ICU stay allows an improvement in the muscle function at hospital discharge compared to patients receiving the standard care.


Description:

Due to medical advances and quality of care, mortality in adult intensive care units (ICUs) has decreased significantly in recent years, leading to a significant increase in the number of patients with high rehabilitation needs on discharge from the ICU. Indeed, these patients are at high risk of complications related to their ICU stay (cognitive impairment, ICU acquired weakness, diaphragm dysfunction, ICU polyneuropathy, post-traumatic stress, malnutrition, etc.). Despite prolonged periods of rehabilitation, there is a significant decrease in functional status and quality of life compared to the previous status of these patient. A specific management by a multidisciplinary team has been set up since 2017 at the Geneva-ICU for long-stay patients (hospitalised ≥ 7 days) including special attention to weaning from ventilation, nutrition, mobilisation, anxiety, pain, skin condition etc. The culture of nutritional therapy and early mobilisation is already well established at the Geneva-ICU. However, a comprehensive approach to nutrition and mobilisation during and after the ICU stay could be optimised. The objective of the study is to determine whether optimization of nutritional therapy combined with early mobilization for patients with long ICU stay will improve muscle function at discharge compared with patients receiving standard care.


Recruitment information / eligibility

Status Recruiting
Enrollment 164
Est. completion date September 2024
Est. primary completion date June 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: Any patient admitted to the adult ICU : - =18 years old - On mechanical ventilation with an expected length of stay = 7 days - Requiring artificial nutrition (enteral and/or parenteral nutrition) Exclusion Criteria: Therapeutic withdrawal Pregnant or breastfeeding patients Neurological disorders with motor deficits: - New or pre-existing neuromuscular or nervous system disease - Spinal cord injury Severe polytrauma of the lower limbs (amputation etc.) Non-independent ambulation (including walking aids) before ICU admission For organizational reasons not allowing follow-up : - Transfer to another ICU - Patient living abroad from Switzerland - Patient living in nursing homes preceding to ICU admission - Incarcerated patients - Intellectual/cognitive disabilities or language barrier, limiting ability to follow the instructions

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Optimisation of nutrition therapy coupled with early mobilisation
Optimisation of nutrition therapy coupled with early mobilisation with: Optimisation of nutrition therapy during ICU stay Optimisation of physiotherapy during ICU stay Better communication and closer collaboration between physiotherapy and nutrition teams. Optimisation of continuity of the care.
Standard care
Patients will receive nutritional therapy and mobilisation according to local standard procedures.

Locations

Country Name City State
Switzerland Service of Intensive Care, Geneva University Hospital, Geneva

Sponsors (1)

Lead Sponsor Collaborator
HEIDEGGER CP

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Walking distance 6 MWT Hospital discharge or end of the intervention (4 weeks after ICU discharge)
Secondary Walking distance 6 MWT At ICU discharge (if achievable); 6 months post-ICU stay
Secondary Body composition Electrical bio impedance At ICU discharge; at hospital discharge or end of the intervention; at 6 months post-ICU stay
Secondary Body composition Peripheral muscle ultrasound Within the 1st 48 hours post ICU admission, at ICU discharge; at hospital discharge or end of the intervention; at 6 months post-ICU stay
Secondary Grip Strength Handgrip At ICU discharge; at hospital discharge or end of the intervention; at 6 months post-ICU stay
Secondary Gradation of muscle function MRC At ICU discharge; at hospital discharge or end of the intervention; at 6 months post-ICU stay
Secondary Physical functionality PFIT & SPPB At ICU discharge; at hospital discharge or end of the intervention; at 6 months post-ICU stay
Secondary Weight difference Comparison between weight at ICU admission, at hospital discharge and at 6 months post-ICU stay At ICU admission, at ICU discharge; at hospital discharge or end of the intervention; at 6 months post-ICU stay
Secondary Appetite 10-point survey scale At ICU discharge; at hospital discharge or end of the intervention; at 6 months post-ICU stay
Secondary Food intake estimation 3 days food diary At 6 months post-ICU stay
Secondary Quality of life (SF-12) SF-12 At 6 months post-ICU stay
Secondary Return to work/activity preceding to the event Collected during the 6 month post-ICU stay consultation At 6 months post-ICU stay
Secondary Length of ICU and hospital stay Collected in the patient form At ICU and hospital discharge
Secondary Duration of mechanical ventilation Collected in the patient form At ICU discharge
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