Ablewhite Joanne, Thomas Shirley, das Nair Roshan, Jones Fiona, Sprigg Nikola, Wharrad Heather, Drummond Avril
School of Health Sciences, University of Nottingham, Nottingham, UK.
School of Medicine, University of Nottingham, Nottingham, UK.
Clin Rehabil. 2025 Aug;39(8):1080-1091. doi: 10.1177/02692155251350084. Epub 2025 Jun 20.
ObjectiveTo develop and test a novel programme to support post-stroke fatigue management for testing in a future clinical trial.DesignStaged approach to development and preliminary testing. Phases 1 and 2: co-design groups held to agree programme content and resources. Phase 3: training for facilitators developed and delivered. Phase 4: feasibility of programme delivery tested with questionnaires completed at beginning and end, and feedback interviews conducted.SettingCommunity, online.ParticipantsStroke survivors with post-stroke fatigue, carers and healthcare professionals.InterventionPost-stroke fatigue management programme supported by 'buddies' with lived or professional experience of managing fatigue.Main measuresIn phase 4, we examined feasibility of programme delivery (recruitment, retention, engagement and acceptability) and preliminary signals of efficacy.ResultsIn phases 1 and 2 we recruited 23 participants (16 stroke survivors, 2 carers and 5 healthcare professionals) and designed resources. In phase 3, 10 people supported training development: 7 received training to be buddies. In phase 4 we recruited 15 people with fatigue; 13 completed the programme. Of these, 13 completed baseline and 12 follow-up questionnaires. All buddies (7/7) and 12/13 participants were interviewed. Mean number of sessions delivered was 9 (SD 3.24; range 3-13) and ranged from 10 to 60 minutes (mean 28 minutes; SD 10.04). Overall, mean fatigue severity reduced, activity increased, and mood measures improved. Participants and buddies were positive about the programme and believed it was worthwhile.ConclusionsThe programme was acceptable and feasible, with preliminary evidence of efficacy, but some issues need to be addressed in future trial design.
目的
开发并测试一项新型计划,以支持中风后疲劳管理,以便在未来的临床试验中进行测试。
设计
采用分阶段方法进行开发和初步测试。第1和第2阶段:召开联合设计小组会议,商定计划内容和资源。第3阶段:开发并提供针对促进者的培训。第4阶段:通过在开始和结束时完成的问卷以及进行的反馈访谈来测试计划实施的可行性。
地点
社区、在线。
参与者
患有中风后疲劳的中风幸存者、护理人员和医疗保健专业人员。
干预措施
由有管理疲劳的生活经验或专业经验的“伙伴”支持的中风后疲劳管理计划。
主要测量指标
在第4阶段,我们检查了计划实施的可行性(招募、留存、参与度和可接受性)以及疗效的初步迹象。
结果
在第1和第2阶段,我们招募了23名参与者(16名中风幸存者、2名护理人员和5名医疗保健专业人员)并设计了资源。在第3阶段,10人支持培训开发:7人接受培训成为伙伴。在第4阶段,我们招募了15名有疲劳症状的人;13人完成了该计划。其中,13人完成了基线问卷,12人完成了随访问卷。对所有伙伴(7/7)和12/13名参与者进行了访谈。平均授课次数为9次(标准差3.24;范围3 - 13次),每次授课时间为10至60分钟(平均28分钟;标准差10.04)。总体而言,平均疲劳严重程度降低,活动量增加,情绪指标改善。参与者和伙伴对该计划持积极态度,并认为它是有价值的。
结论
该计划是可接受且可行的,有疗效的初步证据,但在未来的试验设计中需要解决一些问题。