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Effect of Mobile Interactive Intervention on Social Function Rehabilitation in Stroke Survivors: A Randomized Controlled Trial

Effect of Mobile Interactive Intervention on Social Function Rehabilitation in Stroke Survivors

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500110444
Enrollment
Unknown
Registered
2025-10-14
Start date
2025-10-20
Completion date
Unknown
Last updated
2025-10-20

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

Conditions

Stroke

Interventions

Intervention group:The mini-program comprises two sequential modules: the Course Learning Module and the Gamified Experience Module. The Course Learning Module forms the core component of the interve
Control group:Participants allo

Sponsors

Shanghai First Rehabilitation Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients who meet the diagnostic criteria for stroke (including both ischemic and hemorrhagic stroke) as defined by the Fourth National Cerebrovascular Disease Conference. 2. Patients with a disease duration of >=3 months since the last stroke onset. 3. Aged between 18 and 80 years. 4. Presence of limb dysfunction, with a modified Rankin Scale (mRS) score between 1 and 4. 5. Stable vital signs. 6. A score of >= 26 on the Montreal Cognitive Assessment (MoCA), indicating normal cognitive function. 7. No significant auditory or linguistic communication barriers. 8. Voluntary participation in the study with a signed informed consent form.

Exclusion criteria

Exclusion criteria: 1. Inability to use a smartphone or complete digital interventions. 2. Comorbid conditions that could confound outcomes (e.g., severe dysphagia, major depressive disorder, advanced cancer, end-stage organ failure). 3. Participation in another concurrent clinical trial. 4. Any other reason considered by the investigators to affect compliance or safety.

Design outcomes

Primary

MeasureTime frame
Social participation;

Secondary

MeasureTime frame
Resilience;Exercise adherence;Physical function;Life space;Physical function;Social network;

Countries

China

Contacts

Public ContactXuan Zhou

Shanghai First Rehabilitation Hospital

m15721570098@163.com+86 157 2157 0098

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 27, 2026