跳至主要内容
临床试验/NCT01744145
NCT01744145终止不适用

Early Pneumonia Intervention to Prevent Chronic Complications in Patients Age 40 and Above

Winthrop University Hospital1 个研究点 分布在 1 个国家目标入组 14 人开始时间: 2012年8月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
入组人数
14
试验地点
1
主要终点
improvement in quality of life indices

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
40 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Diagnosis of CAP or HCAP via radiographic imaging and symptoms of pneumonia Age 40 and above.
  • •Discharge to home.
  • •Ability to read and sign consent.
  • •Ability to perform in procedures/exercise.
  • •Ability to understand educational component of the program.
  • •Antibiotic administration for pneumonia within 12 hours of admission.

排除标准

  • •Severe lung diseases like ILD(Interstitial Lung disease), ARDS (Adult Respiratory Distress Syndrome.)
  • •Ventilator dependent patients.
  • •Discharge to nursing home.
  • •Comorbidity that could limit exercise training.
  • •Dementia, Schizophrenia or any active severe psychiatric disorder.
  • •Any Active Malignancy or diagnosis of Lung malignancy.
  • •Inability to attend program two times per week.
  • •Recent myocardial infarction within two months.
  • •Unstable angina, Heart failure (NYHA class III and IV.)
  • •Patients with pneumonia who did not receive antibiotics within 12 hours of admission.

研究组 & 干预措施

Interventional 60 and above

Active Comparator

Interventional group aged 60 and above

干预措施: Interventional 60 and above (Other)

Control 60 and above

No Intervention

Control group aged 60 and above

Interventional 40-60

Active Comparator

Interventional group aged 40-60

干预措施: Interventional 40-60 (Other)

Control 40-60

No Intervention

Control group aged 40-60

结局指标

主要结局

improvement in quality of life indices

时间窗: one year

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

次要结局

  • improvement in functional status(one year)
  • change in 6 minute walk test(one year)
  • exercise intolerance(one year)
  • immunization(one year)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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