跳至主要内容
临床试验/NCT03951090
NCT03951090已完成不适用

Geriatric Assessment Reporting in Real Time (GARRT) in Non-electively Hospitalized Older Cancer Patients

UNC Lineberger Comprehensive Cancer Center2 个研究点 分布在 1 个国家目标入组 148 人开始时间: 2016年4月25日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
148
试验地点
2
主要终点
Referral rate for GA-identified deficits in intervention and control groups

研究概览

简要总结

This study prospectively evaluates the impact of geriatric assessment reporting in real-time (GARRT) on key hospital based outcomes in a cohort of non-electively hospitalized older (> 70 years) adults with cancer.

详细描述

This study evaluates the impact of geriatric assessment reporting in real-time (GARRT) on key hospital based outcomes in non-electively hospitalized older (> 70 years) adults with cancer. Participants will be randomly assigned to the GARRT group, or the control group. All participants will fill out user friendly questionnaire called the geriatric assessment. The results of the geriatric assessment will be given to the physicians of participants in the GARRT group in real-time. The physicians of participants in the control group will not receive real time results.

This study will compare the referral rates of participants in each group to determine if providing real-time results of the geriatric assessment impact referral rates.

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
70 Years 至 —(Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 70 years or older.
  • English speaking.
  • Admitted to UNC Hospitals non-electively within 72 hours.
  • Biopsy proven solid tumor or myeloma or lymphoma.
  • Newly diagnosed cancer patients for whom active cancer directed therapy is planned within the next six months or patients on active cancer directed therapy either currently or within the previous 6 months.
  • Signed written IRB-approved informed consent.

排除标准

  • Patients meeting any of the following exclusion criteria at baseline will be excluded from study participation. Patients with a life expectancy <6 weeks
  • Patients who are <48 hours post-surgery.
  • Patients who are admitted to an intensive care setting.
  • Patients with acute myeloma lymphoma (AML) or other high grade hematologic malignancies.
  • Patients undergoing bone marrow transplant or admitted to the bone marrow transplant unit.

研究组 & 干预措施

GARRT Arm

Experimental

Participants in this arm complete an brief geriatric assessment, and the results of these assessments are given to providers with recommendations to address deficits identified by the geriatric assessment

干预措施: Results of the brief geriatric assessment (Other)

Control Arm

Active Comparator

Providers of participants of this group will not receive the results of the brief geriatric assessments. These participants will receive standard of care treatment

干预措施: No results of brief geriatric assessments (Other)

结局指标

主要结局

Referral rate for GA-identified deficits in intervention and control groups

时间窗: 2 years

Number of participants with at least one referral for a GA-idenfied deficit

次要结局

  • Referral to Physical and Occupational therapy(2 years)
  • Referral to Geriatic Consultation(2 years)
  • Referral to Clinical Pharmacist(2 years)
  • Referral to Nutritionist(2 years)
  • Referral to psyhcosocial support team(2 years)
  • Physician Reported New information(2 years)
  • Physician Reported Satisfaction(2 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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