Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
NA
160 participants
INTERVENTIONAL
2023-01-01
2026-06-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
It is hypothesised that participants in the intervention group, compared with the control group, will demonstrate the outcomes below at immediately and 3 months post-intervention with respect to baseline: 1) Significant improvement in work ability (primary outcome), 2) Significant improvements in self-efficacy, health-related quality of life (HRQoL), emotional well-being and social skills (secondary outcomes).
Eligible participants will be randomly assigned to receive usual care or PVI with usual care and the control group participants will receive usual stroke care services.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Promoting Community Reintegration for Young Adults With Stroke
NCT04560140
Expressive Arts-based Intervention for Young and Pre-elderly Stroke Survivors
NCT03729648
A Two-Tier Care Management Program to Empower Stroke Caregivers in Hong Kong
NCT03034330
Sit-to-stand Training in Stroke Patient
NCT03273101
Dual-task Training in Chronic Stroke
NCT02270398
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
HEALTH_SERVICES_RESEARCH
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Personal Resource Building and Inclusive Volunteering Intervention (PVI)
All participants in the intervention group will receive the intervention (PVI) in addition to usual care. PVI is a 6-week virtual programme aimed at building up young stroke survivors' personal resources for work through engaging in inclusive volunteering activities.
Personal Resource Building and Inclusive Volunteering Intervention (PVI)
PVI is a 6-week virtual programme aimed at building up young stroke survivors' personal resources for work through engaging in inclusive volunteering activities.
Control
All participants in the control group will receive usual stroke care services such as medical or health services offered by the hospitals or community-based organisations.
Usual care
Usual stroke care services include medical and health services offered by the hospitals or community-based organisations.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Personal Resource Building and Inclusive Volunteering Intervention (PVI)
PVI is a 6-week virtual programme aimed at building up young stroke survivors' personal resources for work through engaging in inclusive volunteering activities.
Usual care
Usual stroke care services include medical and health services offered by the hospitals or community-based organisations.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* been clinically diagnosed with a first-ever or recurrent ischaemic or haemorrhagic stroke,
* living at home,
* Montreal Cognitive Assessment score \>2nd percentile,
* a Modified Rankin Scale of 4 or below (moderately severe disability),
* able to communicate in Cantonese and read Traditional Chinese,
* a regular paid employment at the time of stroke,
* been unemployed for at least 3 months at the time of recruitment.
Exclusion Criteria
* have experienced cerebrovascular events due to tumours,
* have been diagnosed with a mental condition such as depression, schizophrenia or bipolar disorder,
* demonstrate incomprehensible speech or difficulty in comprehending conversations, or
* have or are receiving vocational programmes.
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Chinese University of Hong Kong
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Suzanne HS Lo
Assistant Professor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Suzanne Lo
Role: PRINCIPAL_INVESTIGATOR
Chinese University of Hong Kong
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Suzanne Lo
Hong Kong, , Hong Kong
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
PVI
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.