This is a cross-sectional descriptive-analytical study conducted in 2024. The research population comprised all users of the patient information system in the educational and medical centers of Abadan University of Medical Sciences, from which 200 individuals were selected through stratified random sampling across different job categories (medicine, nursing, paraclinical unit staff, health information technology, pharmacy, and administration). Data were collected through a researcher-developed questionnaire based on the modified DeLone and McLean model, in accordance with the three criteria of system quality, information quality, and service quality. At the beginning of the questionnaire, the importance of the study and the research objectives were explained to the respondents. The first part of the questionnaire gathered demographic information of the respondents, including age, gender, education, job, work experience, computer skills, and working hours with the hospital and educational and medical center information system.
1. Inclusion criteria:
- The HIS users: Only individuals actively using the HIS at health centers of Abadan University of Medical Sciences.
- Staff members: Healthcare staff (doctors, nurses, administrators) directly involved with the HIS.
- Patients with data in HIS: Only patients whose data have been entered into the HIS.
- Based on DeLone and McLean model: Studies must evaluate HIS success based on DeLone and McLean criteria.
2. Exclusion criteria:
- Incomplete data: Users or patients with missing or incomplete data in HIS.
- Non-compliance with model: Participants whose data cannot be assessed based on the DeLone and McLean model.
- Inability to access HIS: Users unable to access or use the HIS due to technical issues.
- Refusal to participate: Participants who do not consent or refuse to take part in the study.
The second part includes 21 questions, divided into system quality (7 questions), information quality (7 questions), and service quality (7 questions), which were created on a five-point Likert scale with responses ranging from very high = 5, high = 4, medium = 3, low = 2, to very low = 1. According to the responses of the samples, the success rate of the information system was determined by calculating the average of the total points obtained (1 to 5). After receiving the code of ethics and permission from the university research council, explanations were provided to the users about the study's objectives and the confidentiality of their responses and opinions. After obtaining oral and informed consent, the questionnaire was completed by them. The inclusion criterion for the study was voluntary and informed consent and working with the HIS, while the exclusion criterion was non-cooperation in the study and incomplete completion of the questionnaire.
The validity of the questionnaire was evaluated by five experts, including three health information management experts and two medical informatics experts. Test-retest reliability (with a 10-day interval) was performed to determine the reliability of the questionnaire. Ten users were asked to answer the questionnaire again after ten days, and the reliability of the questionnaire was confirmed using a correlation coefficient of 86%. To obtain the opinions of the experts, the questionnaires were provided to them through in-person visits. SPSS 26 descriptive statistics software was used to analyze the data.