Evaluation of a novel co-designed ‘Fatigue-o-meter' to tackle post-stroke fatigue
Not Applicable
- Conditions
- StrokeFatigueStroke - IschaemicStroke - Haemorrhagic
- Registration Number
- ACTRN12624000387527
- Lead Sponsor
- niversity of Newcastle
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 10
Inclusion Criteria
Stroke survivors: aged over 18-years of age, living in the community, with self-reported post-stroke fatigue.
Caregivers: Where stroke survivors report living with a caregiver, they will be invited to participate.
Exclusion Criteria
Participants will be excluded if they are unable to actively and effectively participate in the intervention. People who are non-English speaking and cannot be accommodated through interpreting services who can support their participation, or people who have cognitive impairment that limits participation in the online intervention will be excluded from this study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Fatigue[Visual Analogue Scale for fatigue Daily during baseline monitoring phase (A) 3 or 4 weeks duration depending on randomisation<br>and daily during the follow-up phase (A1) 6 weeks duration.]
- Secondary Outcome Measures
Name Time Method