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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06245850
Other study ID # Zhengzhouuniversity
Secondary ID 82071331
Status Completed
Phase N/A
First received
Last updated
Start date June 20, 2021
Est. completion date February 10, 2023

Study information

Verified date February 2024
Source Zhengzhou University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Patients and their families all agreed .


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date February 10, 2023
Est. primary completion date July 25, 2022
Accepts healthy volunteers No
Gender All
Age group 30 Years and older
Eligibility Inclusion Criteria: 1. Conformity to the diagnostic criteria for stroke in the "Diagnostic Essentials of Various Cerebrovascular Diseases" revised by the Fourth National Cerebrovascular Academic Conference, and confirmed by cranial CT or MRI. 2. The course of stroke was 2 weeks to 6 months, with steady conditions and stable vital signs. 3. The age ranged from 30 to 80 years old, with at least a junior high school education. 4. The patients had no serious intellectual, language comprehension and behavioral disorders, and could complete the assessment of scales. 5. Achieving a sitting balance of at least reaches level 3, Brunnstrom stage IV or above, and being able to complete Baduanjin training. 6. The National Institutes of Health Stroke Scale (NIHSS) = 15 points. 7. Conforming to the diagnostic criteria for depression in the "Chinese Experts Consensus on Clinical Practice of Post-Stroke Depression". Exclusion Criteria: The exclusion criteria: 1. Disturbance of consciousness, unable to cooperate with polysomnography (PSG) and scale evaluators. 2. Pre-existing diagnosis of depression before stroke. 3. Severe pre-existing sleep disorders before stroke. 4. Patients with mental illness, immune system disorders, severe liver and kidney dysfunction, and severe cardiopulmonary dysfunction

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Baduanjin
chinese baduanjin
Rational emotive behavior therapy
Rational emotive behavior therapy

Locations

Country Name City State
China Henan Zhengzhou Henan

Sponsors (1)

Lead Sponsor Collaborator
Zhengzhou University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary HAMD score HAMD score: The Hamilton Depression Scale (HAMD) were used to evaluate the depression level of the subjects. The HAMD-17 score is 0-6 points for no depression, 8 7-17 points for mild depression, 18-24 points for moderate depression, and 25-54 points for severe depression. A higher score corresponds to more severe depression. 8 weeks
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