跳至主要内容
临床试验/NCT03298230
NCT03298230Unknown不适用

A Pilot Randomised Controlled Trial of REmotely SuPervised Exercise Training for Patients With Peripheral Arterial Disease: The RESPECT-PAD Trial

University of Manchester0 个研究点目标入组 60 人开始时间: 2018年11月最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
60
主要终点
Absolute Claudication Distance

研究概览

简要总结

Peripheral arterial disease affects around 25% of the UK population aged over 55. Left untreated it can lead to debilitating pain, gangrene, amputation and death. It most commonly affects the lower limbs and in the earlier stages of the disease patients can present with a symptom known as intermittent claudication; pain felt in the legs which stops the patient from walking past a certain distance. Current National Institute for Healthcare and Excellence (NICE) guidelines recommend Supervised Exercise as first line treatment for patients with peripheral arterial disease presenting with intermittent claudication. Supervised exercise employs behaviour changing techniques which enable the patient to modify their lifestyles, improving their claudication symptoms, quality of life and reducing their cardiovascular risk. Despite this treatment being significantly more cost-effective than often employed complex endovascular management, most institutions don't offer such programmes citing lack of resources and compliance from clinicians and patients alike.

The investigators propose a more cost-effective, resource-savvy solution in the form of REmotely SuPervised ExerCise Training (RESPECT). This allows the patient to exercise in the convenience of their own home, at a time of their choosing but still be supervised via fitness tracker technology and an online fitness platform. This randomised controlled trial will attempt to prove its' effectiveness in increasing claudication distance, improving functional ability, decreasing cardiovascular risk and improving quality of life whilst being more cost-effective than the currently recognised national first line treatment. This trial has the potential to revolutionise the management of patients with peripheral arterial disease.

研究设计

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

入排标准

年龄范围
30 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients willing and able to undertake supervised or home-based exercise training aged between 40 and 85
  • Positive Edinburgh questionnaire for intermittent claudication (APPENDIX H)
  • Proven peripheral arterial disease on diagnostic imaging
  • Ankle Brachial Pressure Index (ABPI) <0.9
  • Fontaine Classification (APPENDIX I) of PAD Stage II
  • Conservative management plan agreed for by Consultant Vascular Surgeon.

排除标准

  • Critical limb ischaemia
  • Asymptomatic peripheral arterial disease
  • Ambulation limited by co-morbid condition other than claudication:
  • Severe coronary artery disease, angina pectoris, chronic lung disease, neurological disorder, arthritis, amputation
  • Contraindication to exercise training (AHA guidelines):71 acute MI (within 1 week), unstable angina, uncontrolled cardiac arrhythmias causing symptoms or haemodynamic compromise, active endocarditis, symptomatic severe aortic stenosis, acute pulmonary embolus, acute noncardiac disorder than may be aggravated by exercise such as infection, thyrotoxicosis, acute myocarditis, known physical disability that would preclude safe and adequate testing, known thrombosis of the lower limb, known left main stem coronary stenosis, moderate stenotic valvular heart disease, pulmonary hypertension, hypertrophic cardiomyopathy, atrio-ventricular block.
  • Psychiatric disorder precluding them from consenting for research and/or exercise training
  • Arterial reconstruction in the previous 12 months or planned within the next 6 months.
  • Recent or upcoming major surgery (within 3 months)
  • Unwilling or unable to attend/perform exercise training
  • Non-atherosclerotic cause of PAD
  • Other significant medical problems which impact on the patient's ability to complete a 12-week exercise programme, which could include:
  • malignancy, chronic renal disease, chronic liver disease or anaemia, active substance abuse, dementia

研究组 & 干预措施

REmotely SuPervised Exercise Training

Experimental

12- week home based exercise programme consisting of bi-weekly, hourly sessions at the time and place of the participant's choosing. They will wear a fitness tracker which will automatically upload their exercise data to an online platform which can be monitored by the research team and used to provide additional motivation.

干预措施: REmotely SuPervised Exercise Training (Behavioral)

Supervised Exercise Training

Active Comparator

As per NICE guidance. 12 week, bi-weekly, one hour sessions of supervised exercise training.

干预措施: Supervised Exercise Training (Behavioral)

结局指标

主要结局

Absolute Claudication Distance

时间窗: At 12 weeks

Measured using a G-protocol on treadmill testing

次要结局

  • Cost(12 weeks, 6 months and one year)
  • Adherence(12 weeks, 6 months and one year)
  • Absolute Claudication Distance(6 months and 1 year.)
  • Cardiovascular Risk Factors(12 weeks, 6 months and one year)
  • Initial Claudication Distance(12 weeks, 6 months and one year)
  • Health-related Quality of Line(12 weeks, 6 months and one year)
  • Habitual physical activity levels(12 weeks, 6 months and one year)

研究者

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

Charles McCollum

Professor of Surgery

University of Manchester

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