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Effects of a nurse-led home-based stroke self-management programme for stroke survivors: A randomized controlled trial

Effects of a nurse-led home-based stroke self-management programme for stroke survivors: A randomized controlled trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500101274
Enrollment
Unknown
Registered
2025-04-23
Start date
2025-05-16
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Stroke

Interventions

Experimental group:Nurse-led home-based stroke self-management programme
Control group:Usual care

Sponsors

Kaifeng Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) Age >= 18 years; (2) Clinically diagnosed with ischemic or hemorrhagic stroke confirmed by imaging; (3) Discharged from hospital within the past 3 months; (4) Modified Rankin Scale (mRS) score = 24, indicating normal cognitive function; (6) Resident of the local city and able to complete a 12-week follow-up intervention; (7) Supported by a primary caregiver, with both the patient and family providing informed consent.

Exclusion criteria

Exclusion criteria: (1) Severe dysfunction of the heart, lungs, liver, or kidneys, or diagnosis of malignant tumors; (2) History of psychiatric disorders or severe depression/anxiety; (3) Currently participating in other interventional research projects; (4) Inability to communicate via telephone or WeChat, or to complete remote follow-up; (5) Unwillingness to receive the intervention or inability to complete the full intervention period.

Design outcomes

Primary

MeasureTime frame
self-management;Quality of life;fatigue level;

Secondary

MeasureTime frame
Social participation;health literacy;Engagement in daily activities;

Countries

China

Contacts

Public ContactDu Hua

Kaifeng Central Hospital

beida77@126.com+86 139 3860 9366

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026