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临床试验/ISRCTN35709311
ISRCTN35709311已完成不适用

A feasibility study of a psychologically-informed, community-based walking intervention for stroke survivors

Guy's and St. Thomas' NHS Foundation Trust0 个研究点目标入组 40 人开始时间: 2016年3月17日最近更新:
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

研究者

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