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Internet-delivered Cognitive Behavioural Therapy for Persons With Stroke

Internet-delivered Cognitive Behavioural Therapy for Persons With Stroke: Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05243615
Enrollment
100
Registered
2022-02-17
Start date
2023-03-31
Completion date
2023-09-30
Last updated
2023-03-16

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

Conditions

Anxiety, Depression, Stroke

Keywords

Stroke, Depression, Anxiety, internet-delivered cognitive behaviour therapy

Brief summary

Approximately 30% of people with stroke experience symptoms of depression. Many may benefit from access to mental health services that target unhelpful thoughts, such as cognitive behaviour therapy (CBT), but go untreated due to lack of access to specialized care, costs, remote location, or stigma related to seeking care. Internet Cognitive Behavioural Therapy (ICBT) may overcome these barriers. The stroke ICBT program teaches skills such as challenging unhelpful thoughts, memory and attention, managing related physical symptoms, and pacing through a mix of online learning and weekly contact with a trained Guide. While the program's content was found to be acceptable among individuals after stroke, the program's effectiveness still needs to be evaluated. Thus, the primary purpose of this study is to evaluate if the stroke ICBT program will improve symptoms of depression compared to an attention control group. Individuals in both groups will answer questions about themselves and their injury and describe symptoms of depression, quality of life, and health service use to evaluate its impact on people's wellbeing. The study results will be useful in determining if the ICBT program is effective and whether it should be part of routine clinical practice.

Interventions

BEHAVIORALGuided internet delivered cognitive behavioural therapy

A 10-week internet-delivered cognitive behavioural therapy (ICBT) will be delivered to participants who have sustained a stroke. In addition to the online program, a Guide with experience delivering ICBT will provide support by email or phone call once a week. The Guide will spend approximately 15 minutes per week/per client.

BEHAVIORALStroke rehabilitation mental health education

A 10-week stroke-specific rehabilitation education program for stroke patients in usual care at specialized stroke rehabilitation units. The lessons will include information on spinal cord injury rehabilitation: 1)stroke basics, 2)mental health after stroke, 3)pain after stroke, 4)understanding rehabilitation 5)summary of lessons through an online platform. A Guide will check in with participants once a week to answer any content-related questions. The Guide will spend approximately 15 minutes per week/per client.

Sponsors

London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

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

Inclusion criteria

* 18 years of age or older; * Canadian residents; * diagnosed with a stroke at least 6 months ago; * endorsing symptoms of depression (PHQ-9≥5); 5) suicide risk score \<8 (Suicide Behaviours Questionnaire); * speak and read English; * able to access and be comfortable using computers and the internet; * willing to provide a physician as an emergency contact.

Exclusion criteria

* significant cognitive impairment, a score of \<21 on the Telephone Interview for Cognitive Status; * aphasia, with significant language impairment; * currently involved in another psychotherapeutic intervention; * present with a severe mental health disorder requiring in-person therapy (e.g., severe suicidal ideation, severe substance abuse, a recent history of psychosis or mania).

Design outcomes

Primary

MeasureTime frameDescription
Change in depressionbaseline, 10 weeks, 3 monthsMeasured by Patient Health Questionnaire - 9 Item (PHQ-9), higher scores indicate worse outcomes
Change in anxietybaseline, 10 weeks, 3 monthsMeasured by Generalize Anxiety Disorder - 7 Item (GAD7)higher scores indicate worse outcomes

Secondary

MeasureTime frameDescription
Change in perceived disabilitybaseline, 10 weeks, 3 monthsMeasured by The World Health Organization Disability Assessment Schedule ,(WHODAS), higher scores indicate worse outcomes
Change in quality of life symptomsbaseline, 10 weeks, 3 monthsMeasured by VAS on the EuroQol-5D (EQ5D), higher scores indicate better outcomes
Treatment satisfactionbaseline, 10 weeksMeasured by Internet-CBT Treatment Satisfaction Measure, higher scores indicate greater satisfaction
Treatment credibilitybaseline, 10 weeksMeasured by Treatment Credibility Questionnaire (TCQ) which contains 4 items. The first three items range from 0-9 with higher scores indicating better outcome, and the fourth item ranges from 0-100%, with higher scores indicating greater improvement in functioning.
Self-efficacybaseline, 10 weeks, 3 monthsMeasured by Self-Efficacy for managing Chronic Disease-6 (SEMCD), higher scores indicate better outcomes

Contacts

Primary ContactSwati Mehta, PhD
swati.mehta@sjhc.london.on.ca519-661-2111
Backup ContactShannon Janzen
shannon.janzen@sjhc.london.on.ca519-661-2111

Outcome results

None listed

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