Chronic Respiratory Diseases
Conditions
Interventions
Intervention Group:Digital Home Care Intervention Guided by Roy Adaptation Model (RAM)
Control Group:Routine Care
Sponsors
Yancheng First People's Hospital
Eligibility
Sex/Gender
All
Age
40 Years to 80 Years
Inclusion criteria
Inclusion criteria: Patient Diagnosis: Diagnosed with a chronic respiratory disease, specifically including but not limited to: chronic obstructive pulmonary disease (COPD), asthma, interstitial lung disease (e.g., pulmonary fibrosis), chronic bronchitis, and other known chronic respiratory conditions. Age Range: Middle-aged and older adults aged 45 to 75 years and above, who are capable of understanding the study contents. Living Arrangement: Able to reside in a home environment that meets the basic requirements for home care, and capable of safely using medical equipment and receiving nursing services at home. Informed Consent: The patient and their legal guardian(s) are able to fully understand the study's purpose, procedures, risks, and potential benefits, and voluntarily sign the informed consent form to participate in the study. Self-Management Capacity: The patient possesses a certain degree of self-management ability, capable of adhering to medical advice regarding medication management, health monitoring, and basic lifestyle modifications. Language and Communication: The patient is able to understand and communicate in the language relevant to the study (e.g., Chinese) to ensure effective communication and full comprehension of the care plan.
Exclusion criteria
Exclusion criteria: Here is the English translation of the exclusion criteria, maintaining the same professional and clinical research formatting as the previous list: Comorbidities: Presence of severe psychiatric or neurological disorders (e.g., severe depression, schizophrenia, cognitive impairment) that may impair the patient's judgment and self-management capabilities. Acute Illnesses: Presence of acute respiratory infections, acute pneumonia, or other acute illnesses at the time of enrollment that require immediate hospitalization or emergency intervention. Inability to Cooperate: Inability to comply with the follow-up and assessment requirements of the study protocol due to physical conditions (e.g., severe dyspnea) or other reasons (e.g., cognitive impairment, disability). Participation in Other Clinical Trials: Current participation in other clinical studies or trials that may interfere with or influence the outcomes of this study, potentially compromising the validity of the data. Medical Restrictions: Patients deemed by a physician to be medically unsuitable for participation due to potential health risks, such as the presence of uncontrolled cardiovascular disease or other critical conditions. Pregnant or Lactating Women: Pregnant or breastfeeding women are excluded from this study to avoid potential risks. Medication Interference: Currently receiving pharmacological treatments that may interfere with the study results (e.g., novel targeted therapies or investigational drugs).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Roy Adaptation Model Score; | — |
Secondary
| Measure | Time frame |
|---|---|
| Quality of Life Score; | — |
Countries
China
Contacts
Public ContactPeng Xia
Yancheng First People's Hospital
Outcome results
None listed