Skip to content

Evaluation of a novel co-designed ‘Fatigue-o-meter' to tackle post-stroke fatigue

Evaluation of a novel co-designed psychoeducational tool (the ‘Fatigue-o-meter') to treat post-stroke fatigue

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12624000387527
Enrollment
10
Registered
2024-04-03
Start date
2024-07-01
Completion date
2024-12-23
Last updated
2024-07-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Post-stroke fatigue is a common and debilitating consequence of stroke, affecting over half of all stroke survivors, which can persist for years and interferes with recovery. Education is recommended but stroke survivors report that health professionals provide minimal information about fatigue that is difficult to apply to their daily life. This project will evaluate a co-designed education tool called the Fatigue-o-meter via a proof-of-concept study design.

Interventions

The intervention is a psychoeducational tool that has been co-designed with survivors of stroke, caregivers, health professionals, and researchers. The tool is a booklet that contains information about the topics listed below and interactive questions as self-reflection prompts. Participants will meet online with a health professional once per week, for an 8-week intervention period to work through the 8 different chapters in the booklet. Topics covered during the 8 sessions include: Week 1. Di

The intervention is a psychoeducational tool that has been co-designed with survivors of stroke, caregivers, health professionals, and researchers. The tool is a booklet that contains information about the topics listed below and interactive questions as self-reflection prompts. Participants will meet online with a health professional once per week, for an 8-week intervention period to work through the 8 different chapters in the booklet. Topics covered during the 8 sessions include: Week 1. Discussion about the following topics: Learning about your fatigue and how it may protect you; what does fatigue look like after stroke?; Neuroplasticity and the brain; Week 2. Things that make your fatigue go up or down; Discussion and guided questions for self-reflection of the individual aggravating and easing factors for fatigue. Week 3. Discussion and guided self-reflection questions about the participants fatigue; and their alert zone (what levels of fatigue they are comfortable / uncomfortable with); Week 4. Discussion and guided questions for self-reflection and action planning about how fatigue is variable and can change. In this chapter "Planning for fatigue and using the Fatigue-o-meter" the Fatigue-o-meter is a visual tool that allows participants to "rate their fatigue" across the following zones: no fatigue, alert zone, wipe-out zone. Week 6, Goal setting: Individual goal setting around fatigue levels and participation guided by the health professional. Week 7, Refining your plan for fatigue - review of goal setting, modification as required. Week 8: Putting it all together - final review of goal setting and action planning for the future. A health professional will use the chapters in the booklet to guide conversations and self-reflection during 8 one-on-one sessions across an 8-week duration. Each session will be around 30 minutes duration. Participants will have the choice of receiving the education sessions one-on-one face-to-face at a clinic or one-on-one via videoconferencing. While post-stroke fatigue shares some common features, every person's experience is personal. The intervention will be personalized depending on each participant's experience of post-stroke fatigue. For example, participants will share different and personal triggers for their fatigue and the health professional will assist them to problem solve around these personal factors and develop personal strategies accordingly. Adherence to the program and the content delivered in each session will be monitored by the health professional delivering the intervention and subsequently checked by another member of the research team. The three study phases are as follows: (1) Baseline phase (A): Randomization: The duration of the baseline phase will be randomised for each participant (internal validity) in the dyad as either 3 or 4 weeks. By applying baselines of varying length, the effects of the intervention can be assessed for replication in a way that demonstrates experimental control. (2) Intervention phase (B): The intervention will be delivered over an 8-week duration comprising of 8 individual education sessions with a health professional. (3) Follow-up phase (A1): The follow-up phase will be a 6-week duration with no health professional contact. During the baseline and follow-up phases (A and A1) participants will record their fatigue levels each day at a standardised time of day. During the intervention phase (B) participants will only complete the intervention sessions described above.

Sponsors

University of Newcastle
Lead SponsorUniversity

Study design

Allocation
Non-randomised trial
Intervention model
Other
Primary purpose
Educational / counselling / training
Masking
Blinded (masking used) (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

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.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026