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临床试验/ISRCTN58562962
ISRCTN58562962已完成未知

Feasibility of a multidimensional home-based exercise program for the elderly with structured support given by primary care practices: a single arm trial preparing a randomised controlled trial

Ruhr-University Bochum (Germany)0 个研究点目标入组 91 人开始时间: 2009年3月30日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
91

研究概览

简要总结

  1. 2010 protocol in http://www.ncbi.nlm.nih.gov/pubmed/19686587 2. 2013 results in: https://www.ncbi.nlm.nih.gov/pubmed/22538790 (added 18/09/2019)

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • All participants are recruited consecutively by primary care physicians within prespecified time periods. All patients aged greater than or equal to 70 years who are seen by the physician within his consultation hours within that time period are screened for eligibility for the study. Inclusion criteria include:
  • 1. Aged greater than or equal to 70 years, either sex
  • 2. Medical clearance from the primary care physician to participate in the study
  • 3. Walking ability (with or without walking aid) and ability to get to repeated consultations in the primary care physician's practice
  • 4. Patient being able to cooperate appropriately and to follow the instructions of the home-based activity program (primary care physician's judgement)
  • 5. Patient providing written informed consent

排除标准

  • 1. Intervention doesn't fit into the patient's schedule
  • 2. Untreated arterial hypertension or arterial hypertension despite antihypertensive medication (primary care physician's judgement)
  • 3. Deterioration of an insufficiently controlled diabetes mellitus within the past 3 months (primary care physician's judgement) or HbA1c greater than 10% (if available)
  • 4. Chronic heart failure New York Heart Association (NYHA) grade III - IV
  • 5. Clinically relevant cardiovascular event within the past 3 months (e.g. unstable angina pectoris, myocardial infarction, coronary angiography/angioplasty, cardiac surgery)
  • 6. Clinically relevant cerebrovascular event within the past 3 months (e.g. stroke, recurrent transient ischaemic attack [TIA])
  • 7. Acute psychiatric disorder (e.g. depression)
  • 8. Severe consuming illness
  • 9. Any inpatient surgical procedure within the past 3 months
  • 10. Concurrent participation in another clinical trial

研究者

发起方
Ruhr-University Bochum (Germany)

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