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Development and Psychometric Properties of a Work-Readiness Questionnaire for Stroke Survivors

Development and Psychometric Properties of a Work-Readiness Questionnaire for Stroke Survivors

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600128646
Enrollment
Unknown
Registered
2026-07-23
Start date
2026-07-31
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Stroke (ischemic stroke

Interventions

Observation Group (20 experts, 105 patients):None

Sponsors

zhongda hospital southeast university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria (patients): 1. Age 18-60 years; 2. Imaging (CT/MRI) confirmed ischemic or hemorrhagic stroke; 3. Non-acute phase, >3 months post-stroke; 4. MoCA-BJ score >=22; 5. Basic communication and comprehension ability; 6. Modified Barthel Index >40; 7. Employed before onset (full-time, part-time, or self-employed). Inclusion criteria (experts): 1. Medical doctors and rehabilitation therapists (including occupational therapists and physical therapists) with a background in medicine or rehabilitation-related education; 2. Legally obtained practice qualification certificate; 3. At least five years of clinical or research work experience in the rehabilitation field.

Exclusion criteria

Exclusion criteria: 1. Patients: (1) severe language impairment or consciousness disorder; (2) complicated with severe systemic diseases (e.g., heart failure, renal failure, malignant tumors, etc.); (3) patients or their families lack understanding of the protocol, resulting in poor compliance and inability to complete the study procedures. 2. Experts: (1) unable to participate due to health conditions or time constraints; (2) have conflicts of interest (e.g., participating in competing research projects related to work readiness assessment); (3) unwilling or unable to provide informed consent.

Design outcomes

Primary

MeasureTime frame
Content Validity Index: I-CVI, S-CVI;Feasibility Metrics: Completion Rate, Response Time, Missing Response Rate, Comprehensibility;Reliability Metric: Internal Consistency Reliability (Cronbach's alpha);Validity Metrics: Convergent Validity and Concurrent Validity;

Countries

China

Contacts

Public ContactTang Congzhi

zhongda hospital southeast university

zdkf6248@126.com+86 25 83285168

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026