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Construction and the effects of dyadic coping intervention program of social participation for community-dweling and first-episode stroke

Construction and the effects of dyadic coping intervention program of social participation for community-dweling and first-episode stroke

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400083072
Enrollment
Unknown
Registered
2024-04-15
Start date
2023-07-17
Completion date
Unknown
Last updated
2024-04-22

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

Conditions

Stroke

Interventions

Experimental group (SOC):Patients and spouses in the experimental group received 6 sessions(1 session per 2 week
1 h per session) in 12 weeks, and patients and spouses will participate together. The program themes included daily life, family roles, interpersonal interactions, leisure activities, work and reinteg
Control group (CON):Participants in the control group will receive only standardized discharge health education and phone follow-up visits.

Sponsors

Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients: Participants that meet the following criteria will be included in the study: meet the diagnostic criteria for stroke adopted by the Fourth National Academic Conference on Cerebrovascular Disease and diagnosed as stroke by cranial CT or MRI; first stroke patients; taking home rehabilitation; 18=age<80 years; having stable vital signs after acute treatment, 2 =Modified Rankin Scale score <5 points; having ability to walk 10m independently with or without an assistive device; able to give informed consent. Caregivers: The primary family caregiver for stroke patients; Age (female = 20 years old, male = 22 years old); Has good understanding and communication skills; Informed consent for this study.

Exclusion criteria

Exclusion criteria: Patients: History of psychiatric disease; combined with severe physical disease such as myocardial infarction, malignancy, etc.; with severe cognitive dysfunction (MMSE = 20 points); involved in other similar clinical trials. Caregivers: History of mental illness; Participants in other clinical trials.

Design outcomes

Secondary

MeasureTime frame
Knowledge Questionnaire for Stroke Patients;Stroke-specific Quality of Life Scale (SS-QOL);Modified Rankin Scale;Dyadic Coping Inventory;Zarit Caregiver Burden Interview;

Primary

MeasureTime frame
Impact on Participation and Autonomy Questionnaire;Utrecht Scale for Evaluation of Rehabilitation-Participation;

Countries

China

Contacts

Public ContactLi Yuxia

School of Nursing, Shanghai University of Traditional Chinese Medicine

graceliyuxia@163.com+86 134 8223 0226

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 6, 2026