Skip to content

Intervention study of motivational interviewing on depressive symptom clusters in early stroke patients

Intervention study of motivational interviewing on depressive symptom clusters in early stroke patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200064386
Enrollment
Unknown
Registered
2022-10-06
Start date
2022-05-21
Completion date
Unknown
Last updated
2024-08-12

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

Conditions

Stroke

Interventions

Motivation Interviewing group (MI):Subjects in the intervention group also received motivational interviews on the basis of routine treatment and nursing in the department of neurology. There are four
Control group (Con):Subjects in the control group received routine treatment and nursing in neurology department, including inpatient nursing and discharge plan.

Sponsors

The First Affiliated Hospital of Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged >=18 years; 2. Conform to the diagnostic criteria of cerebrovascular disease; 3. Have the imaging diagnosis basis of CT or MRI; 4. 7 to 28 days after stroke; 5. Self-rating Depression Scale (SDS) score >=53 (SDS score >= 53 indicates depressive symptoms).

Exclusion criteria

Exclusion criteria: 1. Serious cognitive and communication disorders 2. Personal or family history of mental disorders; 3. Serious illness or unstable physical condition; 4. Known to leave the area after discharge; 5. Have received mental or clinical psychological intervention.

Design outcomes

Primary

MeasureTime frame
Self-rating Depression Scale,SDS;

Secondary

MeasureTime frame
Stroke Specific Quality of Life,SS-QOL;Pittsburgh sleep quality index, PSQI;

Countries

China

Contacts

Public ContactYang SuiLi

The First Affiliated Hospital of Wenzhou Medical University

1466295833@qq.com+86 135 8768 8033

Outcome results

None listed

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