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Feasibility Randomised-Controlled Trial of Online Stroke Interventions

Primary Purpose

Stroke

Status
Recruiting
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Getting things done after stroke
Stroke psychoeducation
Sponsored by
University of East Anglia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Stroke focused on measuring Stroke, Executive Functions, Goal Management, Problem-Solving, Psychoeducation, Telerehabilitation

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • University of East AngliaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

'Getting things done after stroke' - an online executive function intervention

Stroke psychoeducation

Arm Description

Outcomes

Primary Outcome Measures

Recruitment Rate
Rate of participants recruited into the trial amongst all participants screened
Exclusion Rate
Rate of participants excluded from participating amongst all participants screened
Attrition Rate
Rate of participants and data lost
Follow-up rate
Rate of participants included at 1-month follow-up
Time required to collect and analyze data
Time required for data collection per participant and final analysis
Questionnaire reminders
Number of questionnaire reminders sent and time taken per participant
Support to complete questionnaires
Number of participants requiring support to complete questionnaires and time taken per participant

Secondary Outcome Measures

The stroke self-efficacy scale (SSES; Jones et al., 2008)
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).
The Short Warwick-Edinburgh Mental Wellbeing Scale (SWEMWBS, Tennant et al., 2007)
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)
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)
A 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)
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 survey
A mixture of open-ended (free text response) and closed (Likert type response) questions to assess trial and intervention acceptability.

Full Information

First Posted
June 30, 2022
Last Updated
July 14, 2022
Sponsor
University of East Anglia
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1. Study Identification

Unique Protocol Identification Number
NCT05461937
Brief Title
Feasibility Randomised-Controlled Trial of Online Stroke Interventions
Official Title
A Feasibility Randomised-Controlled Trial of Two Online Psychological Interventions for Stroke Survivors
Study Type
Interventional

2. Study Status

Record Verification Date
July 2022
Overall Recruitment Status
Recruiting
Study Start Date
June 10, 2022 (Actual)
Primary Completion Date
September 15, 2023 (Anticipated)
Study Completion Date
September 15, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of East Anglia

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

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).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke
Keywords
Stroke, Executive Functions, Goal Management, Problem-Solving, Psychoeducation, Telerehabilitation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
'Getting things done after stroke' - an online executive function intervention
Arm Type
Experimental
Arm Title
Stroke psychoeducation
Arm Type
Active Comparator
Intervention Type
Behavioral
Intervention Name(s)
Getting things done after stroke
Intervention Description
A two-session, online rehabilitation intervention focussing on cognitive executive functions supplemented with weekly homework tasks.
Intervention Type
Behavioral
Intervention Name(s)
Stroke psychoeducation
Intervention Description
A two-session, online stroke psycho-education intervention supplemented with weekly homework tasks.
Primary Outcome Measure Information:
Title
Recruitment Rate
Description
Rate of participants recruited into the trial amongst all participants screened
Time Frame
Through study completion, approximately 15 months.
Title
Exclusion Rate
Description
Rate of participants excluded from participating amongst all participants screened
Time Frame
Through study completion, an average of 15 months.
Title
Attrition Rate
Description
Rate of participants and data lost
Time Frame
Through study completion, an average of 15 months.
Title
Follow-up rate
Description
Rate of participants included at 1-month follow-up
Time Frame
Through study completion, an average of 15 months.
Title
Time required to collect and analyze data
Description
Time required for data collection per participant and final analysis
Time Frame
Through study completion, an average of 15 months.
Title
Questionnaire reminders
Description
Number of questionnaire reminders sent and time taken per participant
Time Frame
Through study completion, an average of 15 months.
Title
Support to complete questionnaires
Description
Number of participants requiring support to complete questionnaires and time taken per participant
Time Frame
Through study completion, an average of 15 months.
Secondary Outcome Measure Information:
Title
The stroke self-efficacy scale (SSES; Jones et al., 2008)
Description
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).
Time Frame
Baseline, post-intervention and at 1-month follow-up.
Title
The Short Warwick-Edinburgh Mental Wellbeing Scale (SWEMWBS, Tennant et al., 2007)
Description
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).
Time Frame
Baseline, post-intervention and at 1-month follow-up.
Title
Revised Dysexecutive Questionnaire (DEX-R; Simblett, Ring & Bateman, 2016)
Description
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).
Time Frame
Baseline, post-intervention and at 1-month follow-up.
Title
The Patient Health Questionnaire-9 (PHQ-9)
Description
A 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).
Time Frame
Screening
Title
The ICECAP-A (ICEpop CAPability measure for Adults; Al-Janabi, Flynn & Coast, 2012)
Description
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.
Time Frame
Baseline, post-intervention and at 1-month follow-up.
Title
Feedback survey
Description
A mixture of open-ended (free text response) and closed (Likert type response) questions to assess trial and intervention acceptability.
Time Frame
Post-intervention.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Crina G Ene, MSc
Phone
01603251600
Email
C.Ene@uea.ac.uk
First Name & Middle Initial & Last Name or Official Title & Degree
Catherine EL Ford, PhD
Phone
01603251600
Email
Catherine.Ford@uea.ac.uk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Catherine EL Ford, PhD
Organizational Affiliation
University of East Anglia
Official's Role
Study Director
Facility Information:
Facility Name
University of East Anglia
City
Norwich
State/Province
Norfolk
ZIP/Postal Code
NR5 9HB
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Crina G Ene, MSc
Phone
01603251600
Email
C.Ene@uea.ac.uk
First Name & Middle Initial & Last Name & Degree
Catherine EL Ford, PhD
Phone
01603251600
Email
Catherine.Ford@uea.ac.uk
First Name & Middle Initial & Last Name & Degree
Crina G Ene, MSc
First Name & Middle Initial & Last Name & Degree
Catherine EL Ford, PhD
First Name & Middle Initial & Last Name & Degree
Fergus Gracey, PhD

12. IPD Sharing Statement

Plan to Share IPD
No

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Feasibility Randomised-Controlled Trial of Online Stroke Interventions

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