Effect of Neurophysiological Facilitation Techniques in Intensive Care Patients

Intensive Care Unit Acquired Weakness Clinical Trial

Official title:

Effect of Neurophysiological Facilitation Techniques on Functional Levels and Respiratory in Intensive Care Patients

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05282576
• Other study ID #: Saglik Bilimleri Uni
• Status: Completed
• Phase: N/A
• Start date: October 1, 2019
• Est. completion date: March 1, 2020

Study information

• Verified date: March 2022
• Source: Saglik Bilimleri Universitesi
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The aim of this study was to investigate the effect of neurophysiological facilitation techniques on respiratory and functional levels in intensive care patients. Participants were divided into two groups as experimental (n=20) and control (n=20). Conventional physiotherapy, which includes chest physiotherapy, mobilization exercises and range of motion exercises were applied in control group. Neurophysiological facilitation techniques in addition to the conventional physiotherapy program ere applied in experimental group. The functional status, lower and upper extremity muscle strength, grip strength measurements of the patients and the rates of weaning from mechanical ventilation were evaluated before and after treatment. Vital signs, dyspnea and fatigue perception were assessed each day of treatment. Evaluations were analyzed statistically using Statistical Package for the Social Sciences-22 program.

Description:

The intensive care unit is a multidisciplinary unit in which patients with acute, life-threatening organ dysfunction or under risk are monitored and treated comprehensively. Advanced technology is used for follow-up and treatment in intensive care. These supports decrease the mortality rate. However, the increase length of stay in the ICU leads to higher hospital costs in addition to serious secondary pathologies. Prolonged immobilisation in the intensive care unit(ICU); causes the loss of muscle mass and strength of the patients. When the course of illness, the medical devices used, various medications, malnutrition and other reasons such as sepsis are accompanied by this immobilization, the disorder called Intensive Care Acquired Muscle Weakness (ICU-AW) occurs. This neuromuscular disorder, also causes functional impairments after ICU discharge. Early physiotherapy intervention in ICU, has a positive effect on the symptoms frequently occur in patients. In addition to improve the functional status of the patient such as exercise capacity, muscle strength and mobilization, its increase weaning from mechanical ventilation, and decrease the length of stay in the ICU and hospital. It also provides airway clearance, reduction the work of breathing and improvement of respiratory function. Neurophysiological facilitation of respiration is the use of proprioceptive and tactile stimulation that produce reflexive movement responses. These responses provide to increase the depth of breathing, decrease respiratory rate in patients with decreased level of consciousness. It also increase inspiratory expansion of the ribs, epigastric excursion and abdominal muscles tone. In the study conducted Kumar et al. has indicated that neurophysiological facilitation (NPF) techniques improves levels of dyspnea and oxygen saturation (spO2) in Coronavirus patients. It is very important to increase the level of oxygen saturation to rate the mortality. In NPF techniques, respectively the proprioceptors and tactile receptors in the abdominal, intercostals and spinal muscles are affected, phrenic motor neurons are stimulated, thoracic and abdominal excursions are increased and thus provide improves vital parameters.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 40
• Est. completion date: March 1, 2020
• Est. primary completion date: February 1, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 85 Years

Eligibility

Inclusion Criteria:

• Clinically Unstable
• Participants Over the Age of 18
• Individuals who volunteered to participate in the study or were allowed by their first-degree relatives if they were unconscious.
• Patients who are suitable for physiotherapy by the intensive care specialist.

Exclusion Criteria:

• Having coagulation disorder (INR > 1,5 platelet<50.000 mm3)
• Having neuromuscular diseases
• Having psychiatric disease or overly agitated (Richmond Agitation Sedation Scale score = +2)
• Having acute stroke
• Having Raised Intracranial Pressure Syndrome symptoms
• Having cardiac and respiratory instability (Respiratory frequency > 30 breaths/min,Partial pressure of oxygen(PaO2)< 65 mmHg , fraction of inspired oxygen(FiO2)>%55, Diastolic blood pressure < 50 mmHg or > 200 mmHg , Systolic blood pressure < 80 mmHg or > 200 mmHg)
• Having hemodynamic instability (intropin dose > 5 mcg/kg/min)
• Fever
• Malignity
• Shock
• Patients admitted to ICU after cardiac, trauma and surgery

Related Conditions & MeSH terms

• Intensive Care (ICU) Myopathy
• Intensive Care Unit Acquired Weakness
• Muscular Diseases

Intervention

Other:
• NPF Group
Participants allocated to the experimental group completed until discharged, neurophysiological facilitation(NPF) techniques in addition to conventional physiotherapy.
• Control Group
Critical ill patients was applied their conventional physiotherapy which includes chest physiotherapy and mobilization until discharged

Locations

Country	Name	City	State
Turkey	Istinye University	Istanbul

Sponsors (2)

Lead Sponsor	Collaborator
Saglik Bilimleri Universitesi	Medical Park Hospital Istanbul

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The Chelsea Critical Care Physical Assessment Tool	The Chelsea Critical Care Physical Assessment Tool (CPAx) is a test used on male and female patients in the intensive care unit (ICU) to assess physical and respiratory function impairments and morbidity. The CPAx assessment also identifies patients at risk for developing ICU-acquired complications, such as weakness and mobility decline. The CPAx assesses 10 domains including respiratory function, cough, bed mobility, supine to sitting on edge of bed, dynamic sitting, standing balance, sit to stand, transferring bed to chair, stepping, and grip strength.	through study completion, an average of 5 days
Primary	Physical Function in Intensive Care Test	Physical Function in Intensive Care Test(PFIT) is specifically for the patient population in the intensive care unit (ICU) who are critically ill. This test can be used to guide exercise prescription within the ICU as well as measure functional recovery. The PFIT-s is a battery outcome measure involving four components: sit to stand assistance, marching on the spot cadence, shoulder flexor and knee extensor strength. The PFIT include 4 items.	through study completion, an average of 5 days
Primary	Premorbid Level of Activity Scales	Premorbid dyspnea was scored according to the American Thoracic Society (ATS) scale. The activities of daily living were recorded as 0 = working; 1 = independent (fully ambulatory and living without any assistance); 2 = restricted (able to live on their own and leave their homes to perform basic tasks, but severally limited in exercise ability); 3 = housebound (cannot leave their homes unassisted or leave their homes rarely, able to perform self-care but unable to do heavy chores such as house cleaning, cannot live alone, and may be institutionalized; and 4 = bedridden or wheelchair-bound	through study completion, an average of 5 days
Secondary	Change in Heart Rate	Heart rate can be quantified easily at the bedside, while preload estimation has traditionally relied on invasive pressure measurements, both central venous and pulmonary artery wedge	During ICU stay
Secondary	Change in Blood Pressure	BP can be measured non-invasively using a sphygmomanometer (BP cuff).	During ICU stay
Secondary	Change in Oxygen saturation	Pulse oximetry is the technique used to measure arterial oxygen saturation in the peripheral blood vessels	During ICU stay
Secondary	Change in Respiratory Frequency	The respiratory frequency is usually measured when a person is at rest and simply involves counting the number of breaths for one minute by counting how many times the chest rises.	During ICU stay
Secondary	Change in Perception of Fatigue	the Perception of Fatigue is was assess to used The Borg Rating of Perceived Exertion(RPE). The Borg RPE scale is a numerical scale that ranges from 6 to 20, where 6 means "no fatigue at all" and 20 means "maximal fatigue.	During ICU stay
Secondary	Change in Perception of Dyspnea	the Perception of Dyspnea is was assess to used The Borg Rating of Perceived Exertion(RPE). The Borg RPE scale is a numerical scale that ranges from 6 to 20, where 6 means "no dyspnea at all" and 20 means "maximal dyspnea'.	During ICU stay
Secondary	The Functional Independence Measure	The The Functional Independence Measure (FIM) is an 18-item instrument measuring a person's level of disability in terms of burden of care. The FIM should be rated by the consensus opinion of a multidisciplinary team, but the evaluation is often performed by a single professional. Each item is rated from 1 (requiring total assistance) to 7 (completely independent). Three independent FIM scores can be generated by summing item scores: a total score (FIM total: 18 items), a motor score (FIM motor: eating, grooming, bathing, dressing - upper body, dressing - lower body, toileting, bladder management, bowel management, and transfers bed/chair/wheelchair, toilet, tub/shower, walk, stairs), and a cognitive score (FIM cognitive: auditory comprehension, verbal expression, social interaction, problem solving, and memory).	through study completion, an average of 5 days
Secondary	Change in Muscle Strength	Change in muscle strength was measured with a Digital Manual Muscle Tester.	through study completion, an average of 5 days
Secondary	Change in Hand Grip Strength	Change in Hand Grip Strength was measured with a Hydraulic Hand Dynamometer.	through study completion, an average of 5 days