Physical Training Program in Patients Hospitalized for Community-acquired Pneumonia

University of Nove de Julho

Status: Completed

Conditions: Pneumonia

Treatments: Other: Experimental group; Other: Control group

Study type: Interventional

Funder types: Other

Identifiers

NCT02103400

CAP2014

Details and patient eligibility

About

Hospitalized patients with community-acquired pneumonia (CAP) have reduced functional capacity, peripheral muscle strength and quality of life. Despite the high incidence and severity has not yet been demonstrated whether a physical training program can change these outcomes. Objectives: To evaluate the effects of an exercise training program in patients hospitalized for CAP, to compare this effects with traditional physical therapy and assess whether the inflammatory markers correlate with the functional status of the patient and type of treatment. Methods: A controlled, prospective, randomized clinical trial. Patients hospitalized for CAP, adults, conscious, hemodynamically stable and independent to walk will be studied. In the first day, a medical history, measured dyspnea, incremental shuttle walk test, Glittre test, measurement of peripheral muscle strength, spirometry, and the application of quality of life questionnaire Shor Form 36 will be held. The measurement of inflammatory markers (C-reactive protein and tumor necrosis factor) will also be held. Patients will be randomized into two groups: one will perform a program of physical training (stretching, active resistance exercises and aerobic exercises) and the other group held the traditional physical therapy (bronchial hygiene, breathing exercises and walking) for eight days. On the tenth day the same assessment will be carried out initially described.

Enrollment: 30 patients

Sex: All

Ages: 18 to 80 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Clinical diagnosis of pneumonia
• Must be able to walk
• Time less than 48 hours of hospitalization
• Age above 18 years
• Conscious and oriented
• Hemodynamically stable

Exclusion criteria

• Patients with other respiratory diseases
• Osteoarticular or cognitive disorders
• Patients who refuse to participate or complete the procedures

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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30 participants in 2 patient groups

Experimental group

Experimental group

Description:

Patients hospitalized for community-acquired pneumonia

Treatment:

Other: Experimental group

Control group

Active Comparator group

Description:

Patients hospitalized for community-acquired pneumonia

Treatment:

Other: Control group