Upper Extremity Theraband Exercises in Intensive Care Patients
NCT ID: NCT06416540
Last Updated: 2024-07-30
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
87 participants
INTERVENTIONAL
2024-05-21
2024-07-29
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Theraband Exercises plus Conventional Physiotherapy and Rehabilitation Group (TB+CPRG)
Upper Extremity Theraband Exercises Program Exercise training will be applied in a total of 3 sets, 30-60 min/session, 5 days/week, 8-10 repetitions/set, depending on the condition of each patient, during the patients' stay in the intensive care unit.
Conventional Physiotherapy and Rehabilitation Program Normal joint range movements, airway clearing techniques, breathing exercises and mobilization will be applied to both groups included in the study by the physiotherapist. These movements will be performed once a day for 10 repetitions.
Theraband Exercises plus Conventional Physiotherapy and Rehabilitation Program
Upper extremity, shoulder flexion, abduction, elbow flexion and wrist extension movements will be applied to the study group by the physiotherapist in combination with the breathing pattern. The program will start with yellow therabant and the difficulty level will be increased according to the patient's condition. Exercise training will be applied in a total of 3 sets, 30-60 min/session, 5 days/week, 8-10 repetitions/set, depending on the condition of each patient, during the patients' stay in the intensive care unit.
Conventional Physiotherapy and Rehabilitation Program Normal joint range movements, airway clearing techniques, breathing exercises and mobilization will be applied to both groups included in the study by the physiotherapist. Hemodynamic and respiratory values for each level are monitored on the monitor. In addition, the patient will be monitored for symptoms such as blackness and dizziness by asking the patient.
Conventional Physiotherapy and Rehabilitation Program
Normal joint range movements, airway clearing techniques, breathing exercises and mobilization will be applied to both groups included in the study by the physiotherapist. Hemodynamic and respiratory values for each level are monitored on the monitor. In addition, the patient will be monitored for symptoms such as blackness and dizziness by asking the patient.
Conventional Physiotherapy and Rehabilitation Group (CPRG)
The control group will receive only conventional rehabilitation treatment. Although the duration of the session varies depending on the patient's condition, it will last approximately 30-60 minutes.
Conventional Physiotherapy and Rehabilitation Program Normal joint range movements, airway clearing techniques, breathing exercises and mobilization will be applied to both groups included in the study by the physiotherapist. These movements will be performed once a day for 10 repetitions.
Conventional Physiotherapy and Rehabilitation Program
Normal joint range movements, airway clearing techniques, breathing exercises and mobilization will be applied to both groups included in the study by the physiotherapist. Hemodynamic and respiratory values for each level are monitored on the monitor. In addition, the patient will be monitored for symptoms such as blackness and dizziness by asking the patient.
Interventions
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Theraband Exercises plus Conventional Physiotherapy and Rehabilitation Program
Upper extremity, shoulder flexion, abduction, elbow flexion and wrist extension movements will be applied to the study group by the physiotherapist in combination with the breathing pattern. The program will start with yellow therabant and the difficulty level will be increased according to the patient's condition. Exercise training will be applied in a total of 3 sets, 30-60 min/session, 5 days/week, 8-10 repetitions/set, depending on the condition of each patient, during the patients' stay in the intensive care unit.
Conventional Physiotherapy and Rehabilitation Program Normal joint range movements, airway clearing techniques, breathing exercises and mobilization will be applied to both groups included in the study by the physiotherapist. Hemodynamic and respiratory values for each level are monitored on the monitor. In addition, the patient will be monitored for symptoms such as blackness and dizziness by asking the patient.
Conventional Physiotherapy and Rehabilitation Program
Normal joint range movements, airway clearing techniques, breathing exercises and mobilization will be applied to both groups included in the study by the physiotherapist. Hemodynamic and respiratory values for each level are monitored on the monitor. In addition, the patient will be monitored for symptoms such as blackness and dizziness by asking the patient.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Being conscious
* Being clinically stable
* Not dependent on mechanical ventilation
* Being deemed suitable for physiotherapy and rehabilitation practices by an intensive care specialist
Exclusion Criteria
* Having cooperation disorders
* Having the progressive neuromuscular disease
* Having any trauma to the chest wall
* Having any deformity of the thorax that will affect breathing
* Having diseases that require constant use of sedative or analgesic agents
* Being in shock stiuation
* Having cardiac and respiratory instability (FiO₂\> 55%, PaO₂\< 65 mmHg, respiratory rate \>30 breaths/min, systolic blood pressure \>200 mmHg or \<80 mmHg, diastolic blood pressure \>100 mmHg or \<50 mmHg)
18 Years
85 Years
ALL
Yes
Sponsors
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Izmir Democracy University
OTHER
Responsible Party
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Betül Taşpınar
Study Director
Principal Investigators
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Pınar Unde Ayvat, Assoc. Prof.
Role: PRINCIPAL_INVESTIGATOR
Izmir Democracy University
Ferruh Taspinar, Prof. Dr.
Role: PRINCIPAL_INVESTIGATOR
Izmir Democracy University
Locations
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Betül TAŞPINAR
Konak, İ̇zmi̇r, Turkey (Türkiye)
Countries
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Other Identifiers
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ICU-THERABAND-35
Identifier Type: -
Identifier Source: org_study_id
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