Skip to content

Protein Supplementation in the Functional Rehabilitation of critical patients

Protein Supplementation Strategies in the Functional Rehabilitation of critical patients: randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-10qjnp65
Enrollment
Unknown
Registered
2025-02-26
Start date
2025-04-01
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nutritional therapy

Interventions

This is a randomized, longitudinal controlled clinical trial, with a quantitative approach, where the intervention will consist of two groups of patients undergoing different protein supplementation s
G07.203.300.456

Sponsors

Universidade de Pernambuco
Lead Sponsor
Hospital Universitário da Universidade Federal do Vale do São Francisco
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients admitted to the Intensive Care Unit - ICU; over 18 years old; of both sexes; with indication of the use of exclusive enteral nutritional therapy; and that they undergo early motor rehabilitation according to the institution's protocol (24 hours after admission to the ICU, without intracranial hypertension, in hemodynamic and respiratory stability)

Exclusion criteria

Exclusion criteria: Patients under 18 years of age; who are on oral feeding; parenteral or mixed; or who have some type of contraindication to undergoing motor physiotherapy; patients with suspected or confirmed brain death; patients in palliative care; pregnant women; patients who have contraindications for using the cycle ergometer (skeletal, dermatological or surgical dysfunction); and Body Mass Index (BMI) greater than or equal to 30kg/m² (obesity)

Design outcomes

Primary

MeasureTime frame
It is expected to find a smaller reduction in the thickness of the quadriceps femoris muscle measured through ultrasound compared to the first forty-eight hours and after seven days (above 1.36 centimeters) between the intervention group and the control group

Secondary

MeasureTime frame
It is expected to find a higher percentage of protein adequacy (above 80%) measured through enteral diet infusion records for seven days in the intervention group compared to the standard group

Countries

Brazil

Contacts

Public ContactIzabelle Araujo

Universidade de Pernambuco

izabelle.araujo@ebserh.gov.br+55 (87) 2101-6504

Outcome results

None listed

Source: REBEC (via WHO ICTRP)