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临床试验/NCT03858192
NCT03858192Unknown不适用

Understanding Acute Sarcopenia: a Time-limited Cohort Study to Characterise Changes in Muscle Mass and Physical Function in Older Adults Following Hospitalisation

University of Birmingham1 个研究点 分布在 1 个国家目标入组 168 人开始时间: 2019年5月3日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
入组人数
168
试验地点
1
主要终点
Physical function

研究概览

简要总结

This study aims to characterise acute changes in muscle mass, strength, physical performance in hospitalised older adults. We will assess the impact of these changes upon physical function at three month follow-up, and assess for the impact of clinical and immune-endocrine factors upon these changes.

详细描述

Study Design

Time-limited cohort study involving serial measurements of Bilateral Anterior Thigh Thickness (BATT) using ultrasound, handgrip strength, physical performance, and physical function measured using the Patient Reported Outcome Measures Information System (PROMIS®). We aim to fully characterise changes in these patients, and will perform a comprehensive evaluation of clinical factors including nutrition and physical activity, and measure immune-endocrine markers of inflammation.

Study Participants

Elective colorectal surgery, emergency abdominal surgery, and medical patients aged 70 years and older

Planned Size of recruitment target

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Diagnostic
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

  • ELECTIVE COHORT
  • Aged 70 years or older at time of recruitment
  • Expected to undergo an elective major colorectal surgery procedure
  • EMERGENCY SURGERY COHORT
  • Aged 70 years or older at time of recruitment
  • Emergency admission
  • Expected to undergo emergency abdominal procedure during admission, or emergency abdominal procedure performed within previous 48 hours
  • MEDICAL COHORT
  • Aged 70 years or older at time of recruitment
  • Emergency admission for acute bacterial infection or presumed acute bacterial infection

排除标准

  • ELECTIVE COHORT
  • Unable to provide written informed consent at time of recruitment
  • Unable to understand verbal English
  • Life expectancy less than 30 days
  • EMERGENCY SURGERY COHORT
  • Unable to provide written informed consent at time of recruitment and no consultee available
  • Unable to understand verbal English
  • Life expectancy less than 30 days
  • MEDICAL COHORT
  • Unable to provide written informed consent at time of recruitment and no consultee available
  • Unable to understand verbal English
  • Life expectancy less than 30 days

研究组 & 干预措施

Elective colorectal surgery

Experimental

Patients who are expected to undergo a major colorectal surgery procedure will be recruited to this study preoperatively and followed-up until three months postoperatively.

干预措施: Colorectal surgery procedure (Procedure)

Emergency abdominal surgery

Experimental

Patients who are admitted as an emergency and undergo abdominal surgery will be recruited from general surgery wards either preoperatively or within 48 hours of surgery. They will be followed-up until three month postoperatively.

干预措施: Emergency abdominal surgery (Procedure)

Medical patients

Experimental

Patients admitted under general medicine with an infection will be recruited from general medicine wards within 48 hours of admission. They will be followed-up until three month post-admission

干预措施: Antibiotics (Drug)

结局指标

主要结局

Physical function

时间窗: Three months

Change in physical function at three months as measured by the T score derived from the Patient Reported Outcome Measures Information System (PROMIS®) - Item Bank v. 2.0, Physical Function, Short Form 10b. This is a patient-reported outcome measure of physical function. Raw scores are collected out of a maximum of 50; minimum of 10. These are converted to T scores, which are used for analysis (mean 50, SD 10; range 13.8 - 61.3). Higher scores are representative of better physical function.

次要结局

  • Short Physical Performance Battery (SPPB)(Three months)
  • Bilateral Anterior Thigh Thickness (BATT)(Three months)
  • Acceptability (patient-reported)(Three months)
  • Handgrip strength(Three months)
  • Acute changes during hospitalisation - gait speed(One week)
  • Acute changes during hospitalisation - BATT(One week)
  • Acute changes during hospitalisation - handgrip strength(One week)
  • Rectus femoris echogenicity (quantified using ImageJ software)(Immediately postoperatively, one week postoperatively, and at three months)
  • BATT: subcutaneous tissue ratio (BATT-SCR)(Immediately postoperatively and one week postoperatively)
  • Acute sarcopenia(One week postoperatively)
  • Physical activity - steps taken(One month)
  • Physical activity - distance walked(One month)
  • Sedentary time(One month)
  • Acceptability (objective) - refusal(Three months)
  • Acceptability (objective) - missing data(Three months)
  • Acceptability (objective) - drop-outs(Three months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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