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NCT05902195Recruiting

Improving Work Ability of Young Adults With Stroke

Improving Work Ability of Young Adults With Stroke Through Personal Resource Building and Inclusive Volunteering: A Randomised Controlled Trial

Source: ClinicalTrials.gov · Last updated 11 May 2026

Brief summary (registry, in English)

This project will investigate effects of a novel theory-driven 6-week virtual Personal Resource Building and Inclusive Volunteering Intervention (PVI) on young stroke survivors' work ability, self-efficacy and psychosocial outcomes. 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.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
160 (estimated)
First submitted
5 Jun 2023
Start date
1 Jan 2023
Primary completion date
31 Dec 2027
Lead sponsor
Chinese University of Hong Kong
Diseases
Stroke
NCT number
NCT05902195

What you commit to

  • Study type: Interventional
  • Planned participants: 160
  • From 1 Jan 2023 to the primary completion date, 31 Dec 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • have or are receiving vocational programmes.

Other illness

  • have been diagnosed with a mental condition such as depression, schizophrenia or bipolar disorder,

Other

  • have been diagnosed with transient ischaemic attack,
  • have experienced cerebrovascular events due to tumours,
  • demonstrate incomprehensible speech or difficulty in comprehending conversations, or

Who the study is looking for

  • 18-64 years old,
  • 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.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Suzanne Lo
Coordinator of this site? Confirm its status
Hong KongHong Kong SAR ChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.