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临床试验/NCT03055299
NCT03055299已完成不适用

Comprehensive Exercise (COMEX) Program for Dialysis Patients Pilot Study

University of Pittsburgh1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2017年2月20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
40
试验地点
1
主要终点
Recruitment rate

研究概览

简要总结

The goal of the COMprehensive EXercise (COMEX) pilot study is to test feasibility, tolerability and adherence of this novel video-based intra-dialytic chair exercise program for hemodialysis patients over 3 months.

详细描述

The investigators incorporated patient-provider preferences of the key stakeholders, and used a multi-disciplinary team with experts in physical therapy, psychology and nephrology to develop a comprehensive exercise program for HD patients. Aim of this pilot study is to assess the feasibility, tolerability and adherence to COMEX over 3 months and inform design of future randomized controlled trial. A secondary goal is to explore molecular mechanisms in muscle and blood of exercise adaptation in HD patients

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •For patients:
  • •Age ≥18 years to 85 years
  • •Undergoing maintenance hemodialysis for >3 months at one of the participating dialysis sites
  • •Patients must be willing and able to sign the consent form.
  • •For providers:
  • •Eligible if they are a registered nurse, dialysis technician, dialysis social worker, dietitian, dialysis unit administrator or nephrologist involved in providing care for one of the patient participants in the study

排除标准

  • •For all patients:
  • •Uncontrolled BP (>180/100 mm Hg)
  • •Inadequately dialyzed (Kt/V<1.2)
  • •History of Intradialytic hypotension (SBP<90mm Hg) or hypertension (SBP>180mmHg) during/post dialysis within last 1 month
  • •Contraindication to exercise eg unstable angina, uncompensated congestive heart failure
  • •Refractory/untreated psychiatric disorders
  • •History of poor adherence to HD treatment.
  • •Scheduled for living donor kidney transplant, intention to change to peritoneal dialysis, home HD, or plans to relocate to another center within the next 6 months.
  • •Currently in acute or chronic care hospital
  • •Life expectancy < 6 months or intention to withdraw dialysis therapy within 6 months.
  • •Current pregnancy, or actively planning to become pregnant in the next 6 months
  • •Currently a prisoner
  • •Current use of investigational drugs or participation in another non-observational clinical trial that contradicts or interferes with the therapies or measured outcomes in this trial
  • •Unable or unwilling to follow the study protocol for any reason (including mental incompetence)
  • •Unable or unwilling to provide informed consent or sign IRB-approved consent form
  • •Has a tunneled dialysis catheter
  • •If diabetic, blood sugar control is not stable
  • •For patients undergoing biopsy and blood draw:
  • •Allergy to lidocaine
  • •Anemia, <10.0 Hgb
  • •Chronic use of oral corticosteroids or other medication that affect muscle function
  • •Any bleeding disorder that would contraindicate biopsy or blood draw such as a history of clinically significant bleeding diathesis (e.g. hemophilia A or B, Von Willebrand's Disease or congenital Factor VII deficiency)

研究组 & 干预措施

COMEX

Experimental

Patients receive comprehensive exercise intervention

干预措施: COMEX intervention (Other)

结局指标

主要结局

Recruitment rate

时间窗: 3 months

Feasibility will be estimated by calculating the % of eligible participants who consent to participate in the study.

Number of participants with exercise-related adverse events

时间窗: 3 months

Tolerability will be measured by assessing exercise related side effects - this will be done by weekly patient interviews and review of medical records

Adherence rate

时间窗: 3 months

Adherence will be calculated as % of participants who complete the 3 month COMEX intervention. Also, adherence to exercise will be calculated as % of exercise sessions completed

次要结局

  • Sleep/Wake Behavior by Actigraphy(3 months)
  • Sleep(3 months)
  • Fatigue(3 months)
  • Depression(3 months)
  • Global health(3 months)
  • Health related quality of life(3 months)
  • Physical functioning(3 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Manisha Jhamb

MD

University of Pittsburgh

研究点 (1)

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