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The mortality rate and quality of life is effected in patients with pneumonia, especially in the older population.
The end point of this study is to improve quality of life by and interventional exercise and education. Patients will be randomized at admission and enrolled into the study. They will be assessed with various performance and quality of life indicators before, during and after the study, and exercise tolerance will be assessed throughout and after.
The purpose of this research study is to assess improvement in functional status and quality of life of patients 40 years of age and older patients hospitalized for community acquired pneumonia and healthcare associated pneumonia with a multi-disciplinary program of exercise, education and psychological support. This study will use a randomized, controlled clinical trial design. The total number of patients enrolled will be 120, divided into two groups of 60 patients each. One group will have patients age 40 to 60 and second group will have patients age 60 and above. Stratified randomization will be done to divide these into two (control group and intervention group) equal groups with 30 patients each. The primary endpoint is improvement in quality of life indices. Secondary endpoints are improvement in functional status, change in 6 minute walk test, exercise intolerance, immunization, occult desaturation and change in body weight of patients hospitalized for community acquired pneumonia with a multi-disciplinary program of exercise, education and, psychological support. Eligibility includes age 40 and above at the time of admission, diagnosis of CAP and HCAP via radiographic and PNA symptoms, discharge to home, ability to read and sign informed consent to participate, ability to perform procedures/exercises involved in the study and ability to comprehend educational component of program.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Interventional 40-60 | Active Comparator | Interventional group aged 40-60 |
|
| Control 40-60 | No Intervention | Control group aged 40-60 | |
| Interventional 60 and above | Active Comparator | Interventional group aged 60 and above |
|
| Control 60 and above | No Intervention | Control group aged 60 and above |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Interventional 40-60 | Other | This group will receive the intervention aged 40-60 |
| |
| Measure | Description | Time Frame |
|---|---|---|
| improvement in quality of life indices | patients in the interventional group will undergo exercise and education after a pneumonia infection to see if the quality of life is effected by a rehab program | one year |
| Measure | Description | Time Frame |
|---|---|---|
| improvement in functional status | one year | |
| change in 6 minute walk test | one year | |
| exercise intolerance |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Shalinee Chawla, MD | Winthrop University Hospital | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Winthrop University Hosptial | Mineola | New York | 11501 | United States |
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| ID | Term |
|---|---|
| D011014 | Pneumonia |
| ID | Term |
|---|---|
| D012141 | Respiratory Tract Infections |
| D007239 | Infections |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
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| Interventional 60 and above |
| Other |
This group will receive the intervention aged 60 and above. |
|
| one year |
| immunization | Patients will be assessed to see if education offered in the interventional group will effect compliance with vaccination. | one year |