ISRCTN35709311已完成不适用
A feasibility study of a psychologically-informed, community-based walking intervention for stroke survivors
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 40
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. Aged > 18 years
- •2. Lives in Lambeth or Southwark
- •3. Discharged from hospital after stroke, and from formal, community-based stroke rehabilitation
- •4. Completed 3-month post stroke SLSR assessment
- •5. People who report walking outside for fifteen minutes at least once in the last 3 months on the version of the Frenchay Activities Index most recently completed as part of SLSR data collection
- •6. No known cognitive impairment at time sent invitation pack (Abbreviated Mental Test (AMT) score is 8/10 or greater at most recently completed SLSR data collection time point)
- •7. Not known to be living in a care home or other institution
- •8. Not taking part in any other research studies (apart from SLSR)
- •9. Able to walk outside their home and has done so for at least 15 minutes in the last 3 months
- •10. Able to understand spoken English to the level required to be able to actively participate in the intervention
- •11. Able to use a telephone and will have consistent access to one during the study.
- •12. Willing to wear an accelerometer to measure their physical activity during the study
- •13. No history of recent falls (any fall in the past 3 months)
- •14. No history of recurrent falls (= 2 falls in past 12 months)
- •15. Has not received, is not currently receiving or on the waiting list for a falls prevention intervention (e.g. falls clinic, strength and balance classes targeted at those at risk of falling, 1:1 physiotherapy to mitigate falls risk)
- •16. Is not currently receiving or awaiting physiotherapy for any health problem
- •17. Is not awaiting hip or knee replacement surgery
- •18. Does not have a cardiac pacing device (the accelerometers used to monitor physical activity in this study may potentially interfere with the operation of cardiac pacing devices)
- •19. No experience of fainting/blackouts since discharge from hospital for most recent stroke
- •20. Does not report walking outdoors for more than 30 minutes consecutively, or if able to walk for 30 minutes consecutively, does not do so on more than 4 days per week
- •21. AMT test score is 8/10 or greater when screened by the study RA over the phone.
- •22. Not currently pregnant
- •23. No known allergy/sensitivity to both hypafix and tegaderm adhesive dressing tape (used to apply the accelerometers)
- •24. Timed up and go test score = 12.34 seconds
排除标准
- •1. Lacking capacity to provide consent
- •2. Aged < 18 years
- •3. Live outside of Lambeth, or Southwark
- •4. Have not been discharged from hospital after their most recent stroke
- •5. Have not completed the 3 month South London Stroke Register follow-up
- •6. Live in a care home or other institution
- •7. Are unable to walk outside at least a little
- •8. Are currently taking part in other research studies
- •9. Have fallen over in the last 3 months
- •10. Have a history of recurrent falls (=2 falls in the last year)
- •11. Currently receiving or on the waiting list for falls prevention intervention (s
- •12. Currently receiving physiotherapy for another health problem
- •13. Awaiting hip or knee replacement
- •14. Have a cardiac pacing device
- •15. Have experienced fainting/blackouts since discharge from hospital for most recent stroke
- •16. Scored 7/10 or less on AMT
- •17. Are currently pregnant
- •18. Are unable to speak English to the level required to actively participate in the intervention
- •19. Are unwilling to wear an accelerometer
- •20. Have an allergy to the components of both Tegaderm and Hypafix
- •21. Completed the timed up and go” test = 12.34 seconds, which indicates a risk of falls
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