Nutritional Status in Subacute Stroke Patients Under Rehabilitation 2.0

NCT06096350 | Recruiting

• 1 other identifier: FDG_Nutristroke2_2023
• Study Type: observational
• Target: 55
• Locations: 1 country
• Sites: 1

Brief Summary

The Nutristroke study's findings revealed a malnutrition scenario in post-stroke patients undergoing rehabilitation. This has highlighted the significance of a correct nutritional status assessment upon admission to a rehabilitation unit. The aim of Nutristroke2, therefore, is the assessment of nutritional status, dietary intake, dysphagia, the presence of stroke-related sarcopenia, and systemic oxidative status in patients with subacute stroke outcomes before and after rehabilitation treatment. A secondary aim is to assess whether there is any correlation between nutritional status, dietary intake, dysphagia, sarcopenia, and systemic oxidative status with rehabilitation outcomes.

Conditions

Stroke

Outcome Measures

Primary Outcomes (46)

• change in Mini Nutritional Assessment scores

  questionnaire of evaluation of nutritional status- scores: 0-30- optimum of nutritional status (24-30) risk of malnutrition (17-23,5) malnutrition (\<17)

  baseline (T0), treatment (6 weeks)

• change in weight in kilograms

  it is a measure of body mass weight expressed in Kg

  baseline (T0), treatment (6 weeks)

• change in height in meters

  it is a measure of body mass height calculated in meters

  baseline (T0), treatment (6 weeks)

• change in value of Body mass Index in kg/(m^2)

  it is a measure wich combine the height and weight values to report Body Mass Index (BMI) expressed in kg/m²; this parameter is valid for adult men and women

  baseline (T0), treatment (6 weeks)

• change in arm, waist and hips circumferences expressed in cm

  a measure of circumferences expressed in cm

  baseline (T0), treatment (6 weeks)

• change in food intake

  detection of food intake by means of food diary (measure of portion of dishes consumed; measure of water assumed). Food diary will include the monitoring of 3 days a week for 6 weeks.

  baseline (T0), treatment (6 weeks)

• change in Bioimpedance analysis (BIA) measurements

  it is a non-invasive measurement of body fat, lean muscle mass and hydration

  baseline (T0), treatment (6 weeks)

• change in concentration of blood levels of haemoglobin in g/dL

  blood measurements of haemoglobin (g/dL)

  baseline (T0), treatment (6 weeks)

• change in concentration of blood levels of lymphocite expressed in count of cells or percentage

  blood measurements of total lymphocyte in count of cells or percentage

  baseline (T0), treatment (6 weeks)

• change in concentration of albumine serum levels in g/dL

  serum measurements of albumin in g/dL

  baseline (T0), treatment (6 weeks)

• change in concentration of glucose serum levels in mg/dL

  serum measurements of glucose in mg/dL

  baseline (T0), treatment (6 weeks)

• change in concentration of triglycerides serum levels in mg/dL

  serum measurements of triglycerides in mg/dL

  baseline (T0), treatment (6 weeks)

• change in concentration of total cholesterol serum levels in mg/dL

  serum measurements of total cholesterol in mg/dL

  baseline (T0), treatment (6 weeks)

• change in concentration of HDL cholesterol serum levels in mg/dL

  serum measurements of HDL cholesterol in mg/dL

  baseline (T0), treatment (6 weeks)

• change in concentration of calcium serum levels in mg/dL

  serum measurements of calcium in mg/dL

  baseline (T0), treatment (6 weeks)

• change in concentration of magnesium serum levels in mg/dL

  serum measurements of magnesium in mg/dL

  baseline (T0), treatment (6 weeks)

• change in score of Controlling Nutritional Status (CONUT)

  is a nutritional scoring tool that is calculated using serum albumin, total cholesterol level, total lymphocyte count

  baseline (T0), treatment (6 weeks)

• change in Geriatric Nutritional Risk Index score

  is an index calculated from Lorentz' standardized weight and albumin

  baseline (T0), treatment (6 weeks)

• change in hand grip strenght test score

  it is a test to measure the maximum isometric strenght of the hand and forearm muscles

  baseline (T0), treatment (6 weeks)

• change in Time Up & Go test (TUG) scores

  The Time Up And Go is a test used to assess mobility, balance, and walking in people with balance impairments. The subject must stand up from a chair (which should not be leant against a wall), walk a distance of 3 meters, turn around, walk back to the chair and sit down - all performed as quickly and as safely as possible. Time will be measured using a chronometer.

  baseline (T0), treatment (6 weeks)

• change in Mann Assessment of Swallowing Activity (MASA)

  The MASA consists of 24 items, and each measured score is converted into a weighted 5 or 10 points, which are then summed to a 200-point maximum score. The total scores are then used to define four categories of aspiration risk, as follows: 170-200, no abnormality; 149-169, mild; 141-148, moderate; ≤140, severe. The MASA score was evaluated by expert speech-language-hearing therapists within three days after admission.

  baseline (T0), treatment (6 weeks)

• change in Functionl Oral Intake Scale (FOIS) score

  the Functional Oral Intake Scale (FOIS) assess a patient's food swallowing capability. This tool is designed to measure the effectiveness of a patient's oral intake.The FOIS has seven levels, each denoting a different type of oral intake ability. ITUBE DEPENDENT (levels 1-3) 1. No oral intake 2. Tube dependent with minimal/inconsistent oral intake 3. Tube supplements with consistent oral intake TOTAL ORAL INTAKE (levels 4-7) 4. Total oral intake of a single consistency 5. Total oral intake of multiple consistencies requiring special preparation 6. Total oral intake with no special preparation, but must avoid specific foods or liquid items 7. Total oral intake with no restrictions

  baseline (T0), treatment (6 weeks)

• change in Barthel index (BI) scores

  The BI is designed to assess the ability of an individual with a neuromuscular or musculoskeletal disorder to care for him/herself. It ranges from 0 to 100, with a higher number meaning better performance in activities of daily living.

  Baseline (T0), Treatment (6 weeks) (T1)

• change in Fugl-Meyer Assessment of Motor Recovery after Stroke for Upper Extremity

  The FMA-UL is a stroke-specific, performance-based impairment index. It is designed to assess motor functioning, sensation and joint functioning in patients with post-stroke hemiplegia. The upper limb portion of the FMA-UL ranges from 0 (hemiplegia) to 66 points (normal upper limb motor performance)

  Baseline (T0), Treatment (6 weeks) (T1)

• change in Motricity Index (MI) scores

  The MI aims to evaluate lower limb motor impairment after stroke, administrated on both sides. Items to assess the lower limbs are 3, scoring from 0 to 33 each: (1) ankle dorsiflexion with foot in a plantar flexed position (2) knee extension with the foot unsupported and the knee at 90° (3) hip flexion with the hip at 90° moving the knee as close as possible to the chin. (no movement: 0, palpable flicker but no movement: 9, movement but not against gravity :14, movement against gravity movement against gravity: 19, movement against resistance: 25, normal:33).

  Baseline (T0), Treatment (6 weeks) (T1)

• change in Numerical Rating Scale (NRS) scores

  The Numeric Rating Scale (NRS) is the simplest and most commonly used numeric scale to rate the pain from 0 (no pain) to 10 (worst pain).

  Baseline (T0), Treatment (6 weeks) (T1)

• change in Neuropathic Pain Four Questions (DN4) scores

  The DN4 used to evaluate presence of neuropathic pain, and consist of a brief interview of four questions answered yes/no: two on what the patient has conceived and two during the exam for the evaluation of hypoesthesia to the touch or sting and the evaluation of allodynia with the skimming of the skin. For each 'yes' a point is assigned. The total score is given by the sum of the individuals. The cut off for the presence of neuropathic pain is '4'.

  Baseline (T0), Treatment (6 weeks) (T1)

• change in Modified Ashworth Scale (MAS) scores

  The MAS is a 6 point ordinal scale used for grading hypertonia in individuals with neurological diagnoses. A score of 0 on the scale indicates no increase in tone while a score of 4 indicates rigidity. Tone is scored by passively moving the individual's limb and assessing the amount of resistance to movement felt by the examiner.

  Baseline (T0), Treatment (6 weeks) (T1)

• change in 10 Meter Walk Test scores

  This test will assess the patient's speed during gait. Patients will be asked to walk at their preferred maximum and safe speed. Patients will be positioned 1 meter before the start line and instructed to walk 10 meters, and pass the end line approximately 1 meter after. The distance before and after the course are meant to minimize the effect of acceleration and deceleration. Time will be measured using a stopwatch and recorded to the one hundred of a second (ex: 2.15 s). The test will be recorded 3 times, with adequate rests between them. The average of the 3 times should be recorded.

  Baseline (T0), Treatment (6 weeks) (T1)

• change in Six-Minute Walking Test (6MWT) scores

  The 6MWT measures the distance a subject covers during an indoor gait on a flat, hard surface in 6 minutes, using assistive devices, as necessary. The test is a reliable and valid evaluation of functional exercise capacity and is used as a sub-maximal test of aerobic capacity and endurance. The minimal detectable change in distance for people with sub-acute stroke is 60.98 meters. The 6MWT is a patient self-paced walk test and assesses the level of functional capacity. Patients are allowed to stop and rest during the test. However, the timer does not stop. If the patient is unable to complete the test, the time is stopped at that moment. The missing time and the reason of the stop are recorded. This test will be administered while wearing a pulse oximeter to monitor heart rate and oxygen saturation, also integrated with Borg scale to assess dyspnea.

  Baseline (T0), Treatment (6 weeks) (T1)

• change in Functional Ambulation Classification (FAC) scores

  The Functional Ambulation Categories (FAC) is a 6-point functional walking test that evaluates ambulation ability, determining how much human support the patient requires when walking, regardless of whether or not they use a personal assistive device.

  Baseline (T0), Treatment (6 weeks) (T1)

• change in three point pinch test

  A pinch grip is a form of precision grip whereby a Pinch dynamometers is pinched in three ways.

  Baseline (T0), Treatment (6 weeks) (T1)

• Changes in the Montreal Cognitive Assessment (MoCA

  The Montreal Cognitive Assessment (MoCA) was designed as a rapid screening instrument for mild cognitive dysfunction. It assesses different cognitive domains: attention and concentration, executive functions, memory, language, visuoconstructional skills, conceptual thinking, calculations, and orientation. Time to administer the MoCA is approximately 10 minutes. The maximum possible score is 30 points.

  Baseline (T0), Treatment (6 weeks) (T1)

• Changes in the Symbol Digit Modalities test at follow-up

  The subject is given a sheet of paper at the top of which is printed the key (9 abstract symbols and 9 corresponding numbers). The key is available to the subject throughout the test. A sequence of 120 symbols, each printed in a square, is presented below the key. Empty squares are located below the squares containing the symbols. In the oral version, the examiner, on a copy of the test sheet, records in the empty squares the numbers the subject associates, orally, with the symbols. The subject has to make as many associations as possible within the 90-sec time limit. The score is the number of correct associations made by the subject.

  Baseline (T0), Treatment (6 weeks) (T1)

• Changes in the kinematic analysis kinetic parameters: Force (N) towards 8 targets

  Kinematic information recorded during the administration of the Evaluation Task provided by Motore, based on a center-out point-to-point reaching activity. The kinetics of the end-effector of the robot will be measured by the robot during reaching tasks performed by the patient against the device. The outcome will be the maximum values towards 8 targets.

  Baseline (T0), Treatment (6 weeks) (T1)

• change in serum levels of systemic oxidative stress (dROMs)

  dROMs test measures circulating hydroperoxides (UCarr)

  Baseline (T0), Treatment (6 weeks) (T1)

• change in serum antioxydant capacity (BAP)

  BAP test measures total antioxidant status in serum in micromol/L

  Baseline (T0), Treatment (6 weeks) (T1)

• change in serum lipidic peroxidation (LP-Cholox)

  LP-cholox test measure the lipidic peroxidation (micromol/L)

  Baseline (T0), Treatment (6 weeks) (T1)

• change in gut microbiote composition

  analysis of Next generation sequencing of 16S rDNA metabarcoding and shotgun metatrascriptomic of stool sample

  Baseline (T0), Treatment (6 weeks) (T1)

• change in sieric I-FABP

  ELISA analysis of sieric Intestinal fatty acid binding protein (I-FABP)

  Baseline (T0), Treatment (6 weeks) (T1)

• change in serum levels of zonuline

  ELISA analysis of sieric zonuline

  Baseline (T0), Treatment (6 weeks) (T1)

• change in serum levels of DAO

  ELISA analysis of sieric diaminoxidase (DAO)

  Baseline (T0), Treatment (6 weeks) (T1)

• change in Serum levels of LPS

  ELISA analysis of sieric Lipopolysaccharide (LPS)

  Baseline (T0), Treatment (6 weeks) (T1)

• change in gut metabolomic composition of stool

  analysis of volatile organic compounds (VOCs) and fecal zonuline in stool

  Baseline (T0), Treatment (6 weeks) (T1)

• change in urine levels of indole and scatole

  chromatographic with fluorimeter analysis of indole levels in urine

  Baseline (T0), Treatment (6 weeks) (T1)

• change in urine levels of VOCs

  analysis of volatile organic compounds (VOCs) in urine

  Baseline (T0), Treatment (6 weeks) (T1)

Secondary Outcomes (1)

• assessment of correlation between nutritional status, dysphagia, sarcopenia, oxidative stress with rehabilitation outcome (see primary outcome)

  Baseline (T0), Treatment (6 weeks) (T1)

Study Arms (1)

patients with stroke

Inpatients admitted to the investigators' rehabilitation facility

Device: robotic assisted intervention; Diagnostic Test: hematochemical analysis; Device: BIA, hand grip; Diagnostic Test: nutritional assessment, MNA,; Diagnostic Test: stool sampling; Diagnostic Test: urine sampling; Device: indirect calorimetry analysis

Interventions

robotic assisted intervention DEVICE

Robotic treatment of the upper limb (30 sessions, 5 times a week) using a set of 4 robotic devices: Motore (Humanware); Amadeo, Diego, Pablo (Tyromotion). The training will include motor-cognitive exercises specifically selected to train spatial attention, vision and working memory, praxis, executive function, and speed of processing.

patients with stroke

hematochemical analysis DIAGNOSTIC_TEST

Blood samples of patients will be collected from patients in the early morning (7:30-9:00 a.m.) after an overnight fast at T0 and at T1. Sera samples will be separated by centrifugation (3,000 rpm, 10 min, and 4 °C), divided into 0.5 mL aliquots, and rapidly stored at -80 °C. Subjects' and reference samples were thawed just before the diagnostic test.

patients with stroke

BIA, hand grip DEVICE

bioimpedentiometric analyses of muscular mass (T0 and T1), muscular force with hand grip

patients with stroke

nutritional assessment, MNA, DIAGNOSTIC_TEST

nutritional status assessment will be performed by: body mass index measurements, (height and weight measurements at T0 and at T1); a Mini Nutritional Assessment survey will be administered to patients at admission; a food questionnaire will be administered to patients during from T0 to T1.

patients with stroke

stool sampling DIAGNOSTIC_TEST

stool will be collected at T0 and at T1

patients with stroke

urine sampling DIAGNOSTIC_TEST

the first morning urine will be collected at T0 and at T1

patients with stroke

indirect calorimetry analysis DEVICE

indirect calorimetry analysis with K5 (COSMED, Italy) during six minute walk test or timed up and go test.

patients with stroke

Eligibility Criteria

• Age: 18 Years - 90 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Probability Sample

Study Population

Patients with first ischemic stroke (of ischemic or hemorrhagic etiology) in the subacute phase (within six months after the acute event), hospitalized at the participating intensive-extensive rehabilitation centers will be included.

You may qualify if:

• stroke patients (hemorrhagic or ischemic) documented through Magnetic Resonance -Imaging (MRI) or Computed Tomography (CT);
• time since stroke event within 6 months
• sufficient cognitive and language skills to understand the instructions related to the administration of the assessment scales and to sign informed consent

You may not qualify if:

• presence of a previous stroke based on the medical history;
• behavioral and cognitive disorders that may interfere with the therapeutic activity;
• other orthopedic or neurological complications that may interfere with the rehabilitation protocol;
• inability to understand and sign informed consent;
• the presence of pacemakers (for interference with bioimpedance measures).

Sponsors & Collaborators

• Fondazione Don Carlo Gnocchi Onlus: lead

Study Sites (1)

Fondazione Don Carlo Gnocchi, Santa Maria della Provvidenza Center

Roma, RM, 00166, Italy

RECRUITING

Related Publications (1)

• Siotto M, Cocco C, Guerrini A, Bertoncini C, Germanotta M, Cipollini V, Cortellini L, Pavan A, Lattanzi S, Galluccio C, Insalaco S, Antonacci E, Ruco E, Aprile IG. Nutritional status in subacute post-stroke patients undergoing rehabilitation treatment: a protocol for a prospective observational study. BMC Sports Sci Med Rehabil. 2025 Jun 2;17(1):138. doi: 10.1186/s13102-025-01174-7.

  PMID: 40457485 DERIVED

Biospecimen

Retention: NONE RETAINED

serum sample

MeSH Terms

Conditions

Stroke

Condition Hierarchy (Ancestors)

Cerebrovascular Disorders; Brain Diseases; Central Nervous System Diseases; Nervous System Diseases; Vascular Diseases; Cardiovascular Diseases

Study Officials

• IRENE APRILE, MD, PhD

  Fondazione Don Carlo Gnocchi Onlus

  PRINCIPAL INVESTIGATOR

Central Study Contacts

IRENE APRILE, MD, PhD

CONTACT

+390633086553; iaprile@dongnocchi.it

MARIACRISTINA SIOTTO, PhD

CONTACT

+390633086552; msiotto@dongnocchi.it

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Director of the Neurorehabilitation Department, Neurologist, Principal Investigator

Study Record Dates

• First Submitted: September 28, 2023
• First Posted: October 23, 2023
• Study Start: May 29, 2024
• Primary Completion: July 1, 2025
• Study Completion: December 1, 2025
• Last Updated: June 18, 2024

Record last verified: 2024-06

Locations

IT (1)