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Feasibility Randomised-Controlled Trial of Online Stroke Interventions

A Feasibility Randomised-Controlled Trial of Two Online Psychological Interventions for Stroke Survivors

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05461937
Enrollment
22
Registered
2022-07-18
Start date
2022-06-10
Completion date
2023-09-15
Last updated
2024-05-29

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

Conditions

Stroke

Keywords

Stroke, Executive Functions, Goal Management, Problem-Solving, Psychoeducation, Telerehabilitation

Brief summary

Many people have difficulties organising their behaviour and problem-solving (also known as executive function difficulties) after stroke. This can have serious, wide-ranging consequences for wellbeing and ability to regain independence. Currently, access to psychological interventions after stroke varies and there is not enough evidence to recommend a specific intervention for executive function difficulties after stroke. A short intervention was designed to help with executive function difficulties by making it easier to set goals and achieve them after stroke. The intervention is designed for online delivery to make it accessible to as many stroke survivors as possible. The present trial aims to investigate the acceptability and feasibility of a single blinded randomized controlled trial of this online executive function intervention (active intervention) compared to an online stroke psychoeducation intervention (control intervention).

Interventions

BEHAVIORALGetting things done after stroke

A two-session, online rehabilitation intervention focussing on cognitive executive functions supplemented with weekly homework tasks.

BEHAVIORALStroke psychoeducation

A two-session, online stroke psycho-education intervention supplemented with weekly homework tasks.

Sponsors

University of East Anglia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Outcomes Assessor)

Eligibility

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

Inclusion criteria

* Diagnosis of stroke * ≥ 18 years of age * Capacitous consent to participate * Access to a computer / tablet, the internet, and an email address

Exclusion criteria

* Another significant mental or physical health condition * Current involvement in another research trial * Severe depression (over 20 on PHQ-9) * Not able to read or understand English * Visual, auditory or motor difficulties of a severity that limit the ability to attend to the content of the interventions, read the Participant Information Sheet or complete the consent form and outcome measures * Not registered with a GP or unwilling to provide GP information (for reporting suicidal ideation concerns

Design outcomes

Primary

MeasureTime frameDescription
Support to complete questionnairesThrough study completion, an average of 15 months.Number of participants requiring support to complete questionnaires and time taken per participant
Recruitment RateThrough study completion, approximately 15 months.Rate of participants recruited into the trial amongst all participants screened
Exclusion RateThrough study completion, an average of 15 months.Rate of participants excluded from participating amongst all participants screened
Attrition RateThrough study completion, an average of 15 months.Rate of participants and data lost
Follow-up rateThrough study completion, an average of 15 months.Rate of participants included at 1-month follow-up
Time required to collect and analyze dataThrough study completion, an average of 15 months.Time required for data collection per participant and final analysis
Questionnaire remindersThrough study completion, an average of 15 months.Number of questionnaire reminders sent and time taken per participant

Secondary

MeasureTime frameDescription
The Short Warwick-Edinburgh Mental Wellbeing Scale (SWEMWBS, Tennant et al., 2007)Baseline, post-intervention and at 1-month follow-up.A 7-item questionnaire covering subjective wellbeing and psychological functioning. Respondents are asked to rate each of the items on a scale of 1 to 5 on the basis of how often they had experienced a symptom over the last 2 weeks (1=none of the time, 2=rarely, 3=some of the time, 4= often, 5=all of the time).
Revised Dysexecutive Questionnaire (DEX-R; Simblett, Ring & Bateman, 2016)Baseline, post-intervention and at 1-month follow-up.A tool for measuring everyday problems experienced with the dysexecutive syndrome. It consists of 37 items and respondents are asked to rate how often they experience difficulties related to executive functioning (0=never, 1=occasionally, 2=sometimes, 3=fairly often, 4=very often).
The Patient Health Questionnaire-9 (PHQ-9)ScreeningA self-report measure of depression consisting of nine items matching the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV) criteria of major depression. Respondents are asked to rate each of the items on a scale of 0 to 3 on the basis of how much a symptom has bothered them over the last 2 weeks (0=not at all, 1=several days, 2=more than half the days, 3=nearly every day).
The ICECAP-A (ICEpop CAPability measure for Adults; Al-Janabi, Flynn & Coast, 2012)Baseline, post-intervention and at 1-month follow-up.A measure of capability for the general adult (18+) population for use in economic evaluation. It comprises five attributes (attachment, stability, achievement, enjoyment, and autonomy). Each capability item has four levels of responses.
Feedback surveyPost-intervention.A mixture of open-ended (free text response) and closed (Likert type response) questions to assess trial and intervention acceptability.
The stroke self-efficacy scale (SSES; Jones et al., 2008)Baseline, post-intervention and at 1-month follow-up.A 13-item measure of confidence for functional performance and aspects of self-management relevant post-stroke. Respondents are asked to rate their confidence that they can do various tasks that may have been difficult after having a stroke using a 4-point scale (0=not at all confident, 3=very confident).

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026