Effect of Therapeutic Modalities on the Physical Fitness and Functional Capacity in Critical Patient

Weakness Clinical Trial

— ICUPT  

Official title:

Effect of Therapeutic Modalities on the Physical Fitness and Functional Capacity in Critical Patient

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01881477
• Other study ID #: ICUPT
• Status: Completed
• Phase: N/A
• First received: October 10, 2012
• Last updated: June 17, 2013
• Start date: August 2011
• Est. completion date: February 2013

Study information

• Verified date: June 2013
• Source: CES University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

CONTEXT: The physical deconditioning in the critically ill patient is favored by prolonged immobilization, which compromises the ability to function. This perpetuates the stays in hospital and intensive care units (ICU). To combat this, there physiotherapy intervention methods that can reverse or reduce their occurrence.

OBJECTIVE: The purpose of this research is to determine the effects of passive movements, assisted active and resisted, and changes of position on grip strength, joint mobility and functional capacity in patients in ICU.

METHODS: A quasi-experimental intervention, before and after, no control group, in which 40 patients in an adult ICU in Medellin, receive physiotherapy care. Electrogoniometry, dynamometry and functional independence measure, will be made before the intervention and serial assessments every four days, until discharge from ICU.

Description:

Intervention study, prospective, comparative before-after, no control group, The sample was chosen for convenience and consisted of all patients during the eight months of the execution of research, met the inclusion and exclusion criteria, ie 23 patients. The recruitment of patients was very limited due to the complexity of their health condition. We included patients older than 18 years, with over 24 hours of stay in the intensive care unit, who were begin physical therapy. We excluded those who were hemodynamically unstable heart disease or severe, severe symptomatic stenosis, decompensated heart failure, uncontrolled arrhythmias, high blood pressure (systolic greater than 200 mmHg, diastolic greater than 110 mmHg), mean arterial pressure below 60 mmHg , uncontrolled systemic disease or end stage; limb with unstable or acute musculoskeletal injury, severe dementia or aggressive behavior that does not allow performing the procedure properly, injury or infection of the central nervous system and neuromuscular diseases which take motor control extremity, patients with inotropic or vasoactive treatment associated with severe sepsis or multisystem dysfunction.

To assess muscle strength in the grip using the Baseline ® hand dynamometer. The range of motion were measured using the electronic goniometer Biometrics ®. Functional capacity was assessed using the Functional Independence Measure (FIM) (8), an instrument that allows the classification of individuals according to the score in independent, partially dependent or dependents.

Range of motion was measured articular shoulder abduction and flexion, hip abduction, dorsiflexion standing collar. Dynamometry was applied during the initial evaluation or after the patient's consciousness allowed, bilaterally, choosing the best score of three. The FIM, was filled out at the foot of the patient bed, by the evaluators. Were followed for clinical outcome in four days of starting treatment, and dynamometry applied only if the state of consciousness allowed. Evaluations were completed once the patient was transferred to the Special Care Unit (SCU).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 24
• Est. completion date: February 2013
• Est. primary completion date: February 2013
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patient with more than 24 hours of stay in the Intensive Care Unit, who is going to start physical therapy.

• A patient who has a family to sign the informed consent and who can provide information for the processing of the instrument.

Exclusion Criteria:

• Heart diseases hemodynamically unstable or severe.

• High blood pressure (systolic, + 200 mm Hg, diastolic, +110 mm Hg).

• Mean arterial pressure below 60 mm Hg.

• Uncontrolled systemic disease or terminal condition.

• Tip with unstable musculoskeletal injury or acute.

• Severe dementia or behaviors that do not allow to perform the procedure properly.

• Injuries and / or infection of the central nervous system.

• Neuromuscular diseases in which motor control lost limbs.

• Patient in ICU inotropic and vasoactive treatment high associated to sepsis and / or severe multisystem dysfunction medication order can not mobilize.

Related Conditions & MeSH terms

• Physical Deconditioning
• Weakness

Intervention

Procedure:
• kinetics modalities
The duration of the intervention will be approximately 30 minutes to 1 hour and will take place 5 days a week. They constantly monitor the vital signs and signs of exercise intolerance. The intervention consists of four levels of complexity. The progression in kinetic patterns based on muscle strength during exercise Kinetic methods begin with passive movements and patients are assisted in the movement slowly until they are active, culminating in movements against resistance, in all joints, with a minimum of 10 repetitions for each joint. Additionally, it promotes the adoption and sitting positions long and short legged and walk.

Locations

Country	Name	City	State
Colombia	Alejandra Mondragón	Medellín	Antioquia

Sponsors (1)

Lead Sponsor	Collaborator
CES University

Country where clinical trial is conducted

Colombia, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Days of mechanical ventilation		6 months
Other	Hospital stay		6 months
Other	ICU stay		6 months
Primary	Range of motion	Evaluate the range of motion in the joints(Shoulder, Knee, Ankle) of the user before and after the physiotherapy intervention	6 months
Primary	hand grip strength		6 months
Secondary	Functional capacity		6 months