Condition 1: Cholecystitis. Condition 2: Chronic Cholecystitis. Acute cholecystitis Chronic cholecystitis
Conditions
Interventions
Intervention 1: Intervention group: Cholecystitis patients who have undergone laparoscopic cholecystectomy surgery and, in addition to the usual training (educational pamphlet and face-to-face trainin
Sponsors
Mashhad University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: Willingness to participate in the study Having a diagnosis of cholecystitis Cholecystitis patients undergoing laparoscopic surgery Age 18-60 years No cognitive impairment Fluency in Persian Access to an Android smartphone
Exclusion criteria
Exclusion criteria: Open cholecystectomy surgery Not using the app at home based on the phone call checklist is more than 50%
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain intensity. Timepoint: pain intensity will be measured during the first 48 hours after surgery using the VAS scale (every 6 hours) and the McGill Pain Questionnaire 6 hours after surgery, the next day, and two weeks later. Method of measurement: pain intensity will be measured during the first 48 hours after surgery using the Visual Analogue Scale (every 6 hours) and the McGill Pain Questionnaire 6 hours after surgery, the next day, and two weeks later. | — |
Secondary
| Measure | Time frame |
|---|---|
| Quality of life. Timepoint: Quality of life will be measured using the GIQLI questionnaire before the intervention and one month later. Method of measurement: Quality of life will be measured using the GIQLI questionnaire before the intervention and one month later. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactElham Safari
Mashhad University of Medical Sciences
Outcome results
None listed