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The Effectiveness of Combined Occupational Therapy and Social Support Group on motor function, social participation and psychological well-being among Stroke Patients

The Effectiveness of Combined Occupational Therapy and Social Support Group on motor function, social participation and psychological well-being among Stroke Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600124817
Enrollment
Unknown
Registered
2026-05-18
Start date
2026-05-18
Completion date
Unknown
Last updated
2026-05-25

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

Conditions

stroke

Interventions

intervention group:An 8-week combined occupational therapy and social support platform intervention. The intervention consists of 2–3 weekly face-to-face occupational therapy sessions alongside engage
Week 2 – Basic Life Skills Training
Week 3 – Emotional Self-awareness and Stress Management
Week 4 – Social Role Reintegration
Week 5 – Upper Limb Motor Rehabilitation
Week 6 – Coping with Anxiety and Confidence Building
Week 7 – Community Participation Practice
Week 8 – Self-reflection and Future Planning.
control group:An 8-week standard occupational therapy intervention. The intervention consists of 2–3 weekly face-to-face occupational therapy sessions.
Focus group discussion participants:None

Sponsors

Wuxi Central Rehabilitation Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Phase 1: (1) Adult patients are diagnosed with stroke, aged between 30 and 65 years. (2) Able to participate in activities on the social support platform. (3) Citizen of China Phase 2: (1) Participants who completed the full 8-week intervention. (2) Willing to share their experiences and provide feedback on the intervention.

Exclusion criteria

Exclusion criteria: 1.Phase 1: (1) Unstable cardiovascular diseases (e.g., myocardial infarction within the past 6 months, NYHA class III-IV heart failure). (2) Terminal malignancies (expected survival 9.0%, SBP >180mmHg). (4) Severe psychiatric disorders (e.g., schizophrenia, bipolar disorder) (American Psychiatric Association 2016). (5) Moderate to severe depression (HAM-D > 17) (Hamilton 1960). (6) Severe motor impairments (Brunnstrom Stage 1, completely flaccid limb) (Brunnstrom 1970). (7) Severe cognitive impairment (MMSE < 27) (Folstein et al. 1975). (8) Severe upper limb dysfunction affecting digital interaction, defined as: i. Brunnstrom Hand Recovery Stages 1-2 (no voluntary hand movement) (Brunnstrom 1970). ii. Fugl-Meyer Upper Extremity Score < 10 (Fugl-Meyer et al. 1975). iii. Failure in smartphone usability test (inability to unlock phone, open a social app, send a basic message, or tap on-screen elements). (9) Inability to participate in the intervention due to severe aphasia or hearing impairment. 2.Phase 2: (1) Individuals with communication impairments that prevent meaningful participation.

Design outcomes

Primary

MeasureTime frame
Motor Function;Social Participation Level;Psychological Well-being;

Secondary

MeasureTime frame
Activities of Daily Living (ADL/IADL);Perceived Social Support;Quality of Life;

Countries

China

Contacts

Public ContactChen Yuxi

Wuxi Central Rehabilitation Hospital

13400693193@163.com+86 134 0069 3193

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 30, 2026