Following respiratory viral infection
Conditions
Interventions
Control Group:The control group received a 12-week standardized health education intervention. The intervention encompassed three key components: First, guidance on optimizing the sleep environment, i
Interventional group:The interventional group received the same health education as the control group, supplemented by a 12-week square dance intervention involving five sessions per week. The interve
Sponsors
Xinwu District Rehabilitation Hospital, Wuxi City
Eligibility
Sex/Gender
Female
Age
55 Years to 70 Years
Inclusion criteria
Inclusion criteria: 1. Female aged 55–70 years; 2. Diagnosed with acute respiratory viral infection within the past month by PCR testing or clinical diagnosis, and currently in the symptom resolution phase; 3. Developed depressive symptoms and insomnia following infection, meeting the ICD-10 diagnostic criteria for non-organic insomnia, with a PHQ-9 score >=5 and an ISI score >=8; 4. Mini-Mental State Examination (MMSE) score >=27, indicating essentially normal cognitive function; 5. No history of major neurological disorders, other serious somatic diseases, or psychiatric disorders in the family; 6. Not on long-term use of sedative-hypnotic drugs, antidepressants, or other medications with significant effects on the central nervous system, mood, or sleep; 7. No motor dysfunction, capable of independently participating in square dancing exercises.
Exclusion criteria
Exclusion criteria: 1. Suffering from severe psychiatric disorders such as dementia, schizophrenia, or bipolar disorder, or secondary insomnia/sleep disturbances caused by other somatic or psychiatric conditions; 2. History of alcohol dependence, misuse of antidepressants or anxiolytics, or continuous use of sedative-hypnotic drugs over the past two weeks with inability to discontinue; 3. Already have a regular exercise routine, engaging in moderate- or higher-intensity physical activity at least >=2 times per week; 4. Presence of balance disorder-related conditions (e.g., severe vertigo, ataxia) or having undergone major surgery within the past three months.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Depression Symptom Screening Scale;Insomnia Severity Index (ISI); | — |
Secondary
| Measure | Time frame |
|---|---|
| Vital capacity;Grip strength;Body Mass Index;Lipid metabolism (including TC, TG, LDL-C, etc.); | — |
Countries
China
Contacts
Public ContactFang Ping
Xinwu District Rehabilitation Hospital, Wuxi City
Outcome results
None listed