The effects of self-care cellphone application on stress, anxiety and depression among admitted patients with COVID-19
Not Applicable
Recruiting
- Conditions
- COVID-19.COVID-19, virus identifiedU07. 1
- Registration Number
- IRCT20170922036314N4
- Lead Sponsor
- Mashhad University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 112
Inclusion Criteria
baseline literacy
having a smartphone
ability to work with smartphone
at least 3 days hospitalization
Exclusion Criteria
Unwillingness to participate in the study
Transfer to wards where it is not possible to use a mobile phone, such as the intensive care unit
Deterioration of the patient's physical condition
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method DASS-21 questionnaire score. Timepoint: Before intervention, at the time of discharge, 2 weeks after discharge. Method of measurement: DASS-21 questionnaire score (including depression, anxiety, stress scales).
- Secondary Outcome Measures
Name Time Method Respiratory rate. Timepoint: Before intervention, at the time of discharge. Method of measurement: physician assessment.;Oxygen saturation. Timepoint: Before intervention, at the time of discharge. Method of measurement: pulse oxymetry.;Lung involvement. Timepoint: Before intervention, at the time of discharge. Method of measurement: radiography.;Multi-organ failure. Timepoint: Before intervention, at the time of discharge. Method of measurement: kidney and liver function tests.;Fever. Timepoint: Before intervention, at the time of discharge. Method of measurement: thermometer.;Secondary infection. Timepoint: Before intervention, at the time of discharge. Method of measurement: physician assessment.