Local Opera Viewing Combined Medical Gymnastics for Elderly PSCI
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Local opera appreciating and Medical gymnastics training.
- Who it may be relevant to
- Registry conditions: Post-stroke Cognitive Impairment. Basic parameters: 60 years — 100 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Construction and Empirical Study of Local Opera Appreciation Combined With Medical Gymnastics Training Program for Elderly Patients With Post-stroke Cognitive Impairment
Overview
local opera viewing combined medical gymnastics for elderly PSCI
Detailed description
Cognitive impairment and hemiplegia are the two major problems faced by elderly patients with cognitive impairment after stroke. The application of local drama viewing and combined medical gymnastics training aims to improve sports and cognitive function. Local drama viewing and medical gymnastics training integrates drama art cognition and medical sports, is a beneficial scientific attempt.
To construct a local opera viewing combined medical gymnastics training program for elderly patients with post-stroke cognitive impairment, and to explore its feasibility, acceptability and safety.
Interventions
- Behavioral Local opera appreciating and Medical gymnastics training
To construct a local opera viewing combined medical gymnastics training program for elderly patients with post-stroke cognitive impairment, and to explore its feasibility, acceptability and safety.
Primary outcome measures
- NIH stroke scale, NIHSS [Time frame: Before and at 3 months after the intervention]
- Muscle strength [Time frame: Before and at 3 months after the intervention]
- Montreal cognitive assessment, MoCA-Beijing [Time frame: Before and at 3 months after the intervention]
- Mini-Mental State Examination, MMSE [Time frame: Before and at 3 months after the intervention]
Secondary outcome measures (5)
- Hamilton Anxiety Rating Scale [Time frame: Before and at 3 months after the intervention]
- Hamilton Depression Rating Scale [Time frame: Before and at 3 months after the intervention]
- Pittsburgh Sleep Quality Index [Time frame: Before and at 3 months after the intervention]
- Stroke Impact Scale，SIS [Time frame: Before and at 3 months after the intervention]
- Subscales of the Functional Assessment of Communication Skills, SFACS [Time frame: Before and at 3 months after the intervention]
Eligibility criteria
Inclusion criteria
Stroke patients who were hospitalized in the Department of Neurology of Zhangzhou Hospital and met the PSCI diagnostic criteria of the Expert Consensus on the Prevention and Treatment of Cognitive Impairment after Stroke in China were the subjects of the study. ① Stroke patients confirmed by neuroimaging, onset time within 1 week; (2) Cognitive impairment occurs after stroke events; ③ The scores of the simple mental state examination scale were points in the illiterate group, points in the primary school group, points in the secondary school group, and points in the college group; ④ can maintain independent sitting position ≥30 min; ⑤ Age ≥60 years old; ⑥ Volunteer to join the study and receive intervention treatment.
Exclusion criteria
- Other causes affect or lead to cognitive impairment, such as consciousness disorder, malignant tumor, severe liver and kidney insufficiency; ② There are serious cardiopulmonary and other systemic diseases; Visual or hearing impairment; ④ have emotional behavior abnormalities and mental illness (including depression); ⑤ A history of alcohol or drug abuse
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Double blind
- Primary purpose
- Supportive care
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT06458348 · Zhangzhou Municipal Hospital