Respiratory system diseases
Conditions
Interventions
Observation group (patient group):None
Observation Group (Family Group):None
Sponsors
Peking University Shenzhen Hospital
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. Patients: (1) Age>=18 years old; (2) Diagnosed with severe respiratory diseases (including chronic obstructive pulmonary disease, acute respiratory distress syndrome, severe pneumonia, etc.) and treated in ICU; (3) ICU admission time>=48h; (4) Those who are about to be transferred to a general ward for treatment after being ordered by a doctor; (5) Be aware and able to cooperate with questionnaires and follow-up; (6) Voluntary participation in the research. 2. Dependents: (1) Age>=18 years old; (2) Be the primary caregiver of the patient and be responsible for their medical decision-making or daily care. Primary caregiver selection for older patients: spouse is the first choice, and if the spouse is unfit to be the primary caregiver for health or other reasons, then the child; Primary caregiver selection for young patients: choice of spouse; (3) Be aware and able to participate in research and follow-up; (4) Voluntary participation in the study.
Exclusion criteria
Exclusion criteria: 1. Patients: (1) ICU admission time within 3 months before the admission >=48h; (2) transfer to other ICUs; (3) The patient is temporarily transferred out of the ICU or temporarily discharged; (4) If the patient returns to the ICU during the observation period, his or her eligibility for participation will be reassessed on a case-by-case basis, and his return to the ICU will be recorded as an important influencing factor; (5) The patient or family member requests to terminate the treatment; (6) Severe hearing impairment, dysarthria, etc., which cannot be followed up; (7) The condition is serious and unable to cooperate with the completion of the questionnaire. 2. Dependents: (1) Previous history of mental illness, severe psychological or cognitive dysfunction; (2) Refusal to continue to participate in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Stress level of the patient during migration;Stress level of family members during migration; | — |
Secondary
| Measure | Time frame |
|---|---|
| The dual coping level of patient;The dual coping level of family members;The level of the patient's perceived social support;The level of family members' perceived social support; | — |
Countries
China
Contacts
Public ContactZhang Wenting
Peking University Shenzhen Hospital
Outcome results
None listed