ISRCTN91163727已完成未知
Developing and evaluating an education programme aimed at increasing physical activity in individuals with diagnosed coronary heart disease: a randomised controlled trial
niversity of Leicester0 个研究点目标入组 291 人开始时间: 2017年2月27日最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 291
研究概览
简要总结
2018 Protocol article in https://www.ncbi.nlm.nih.gov/pubmed/30286797 results 2021 Results article in https://pubmed.ncbi.nlm.nih.gov/33637567/ results (added 01/03/2021)
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •Current participant inclusion criteria as of 13/02/2019:
- •1. Aged 18 years or older
- •2. 12-48 months post confirmed diagnosis of a cardiac event (myocardial infarction, angina or acute coronary syndrome)
- •3. Able to speak and read English to participate effectively in a group education programme
- •4. Willing and able to attend the education sessions and clinic visits
- •5. Willing and able to give informed consent
- •6. Access to a mobile phone in order to receive text messages
- •7. Willingness to allow GP notification of their participation in study and access to patient records for purpose of study
- •8. Able to take part in moderate physical activity as assessed using Incremental Shuttle Walk Test (ISWT) (Level three or above)
- •Previous participant inclusion criteria:
- •1. Aged 18 years or older
- •2. 12-36 months post confirmed diagnosis of a cardiac event (myocardial infarction, angina or acute coronary syndrome)
- •3. Able to speak and read English to participate effectively in a group education programme
- •4. Willing and able to attend the education sessions and clinic visits
- •5. Willing and able to give informed consent
- •6. Access to a mobile phone in order to receive text messages
- •7. Willingness to allow GP notification of their participation in study and access to patient records for purpose of study
- •8. Able to take part in moderate physical activity as assessed using Incremental Shuttle Walk Test (ISWT) (Level three or above)
排除标准
- •1. Individuals with a diagnosis of heart failure where the underlying primary cause is not myocardial disease as a result of atherosclerosis will be excluded from this study
- •2. Musculoskeletal limitations that would limit physical activity (e.g. musculoskeletal injury)
- •3. Participation in another clinical intervention study in the past 12 weeks
- •4. Lacks capacity to give informed consent
- •5. Severe life-threatening co-morbidity (e.g. malignancy)
- •6. Poor exercise capacity, (< level three on the ISWT [120 metres]), these individuals will be directed back into cardiac rehabilitation (good practice)
- •7. Housebound or immobile
- •8. Unstable symptoms (chest pain or breathlessness at rest; unstable stage II hypertension [160/100mmHg], not on necessary medications)
- •9. Individuals with no or limited understanding of written or verbal English
研究者
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