The Effect of Education to be Provided to Patients to Undergo Prostate Surgery With Mobile Application on Patient Outcomes

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The aim of this study was to determine the effect of mobile application training on patient outcomes (preoperative anxiety, surgical fear, postoperative pain, hemodynamic parameters, satisfaction level and length of hospital stay) in patients undergoing transurethral prostate resection surgery. It was planned as a prospective, two-arm (1:1), randomized controlled clinical trial. The study will be conducted with 68 patients in the urology clinic of a vir university hospital. Patients will be randomly assigned to the control group and the mobile application training group. Patients in the mobile application group will be trained with the mobile application, while patients in the control group will only receive routine care in the clinic. Patients assigned to the mobile application group will be introduced to the education to be given with the mobile application and the application will be downloaded to their phones/tablets. Data will be collected with the Introductory Information Form, Visual Comparison Scale, State Anxiety Scale, Hemodynamic Parameters Monitoring Form, Surgical Fear Scale and Discharge Education Satisfaction Scale. When the patient is admitted to the clinic, Introductory Information Form, State Anxiety Scale, and Surgical Fear Scale will be applied to the patients in the mobile intervention and control groups before surgical intervention, and Hemodynamic Parameters Monitoring Form will be completed. After the surgical intervention, Visual Comparison Scale and Discharge Education Satisfaction Scale will be applied to all patients and Hemodynamic Parameters Monitoring Form will be completed. The data will be analyzed in a computer environment.

Eligibility
Participation Requirements
Sex: Male
Minimum Age: 18
Healthy Volunteers: t
View:

• 18 years of age or older,

• Written permission to participate in the study,

• Conscious, oriented and cooperative,

• Speaks and understands Turkish,

• Literate,

• Undergoing TURP,

• No vision problems,

• Patients who or their caregivers have a phone/tablet with the ability to download mobile training

Locations
Other Locations
Turkey
Tarsus University
RECRUITING
Mersin
Contact Information
Primary
Gamze Bozkul
gamze.bozkul@gmail.com
03246000033
Backup
Serpil YÜKSEL
serpilyuksel77@gmail.com
Time Frame
Start Date: 2025-06-03
Estimated Completion Date: 2026-06-01
Participants
Target number of participants: 68
Treatments
Experimental: Mobile application group
When the executive (EP) goes to the patient for the procedure, he/she will fill out the Informed Consent Form, open the envelope and find out which group the patient is in. Introductory Information Form, 'State Anxiety Scale', 'Hemodynamic Variables Monitoring Form' and 'Surgical Fear Scale' will be completed for all patients undergoing TURP. Patients in the study group will be introduced to the training to be given with the mobile application and downloaded to their phones/tablets. According to randomization, patients in the study group will receive training with the mobile application and patients in the control group will receive routine care. In the postoperative period, Hemodynamic Variables Monitoring Form, Visual Analog Scale and Discharge Training Satisfaction Scale will be completed for all patients.
No_intervention: Control group
When the executive (EP) goes to the patient for the procedure, he/she will fill out the Informed Consent Form, open the envelope and find out which group the patient is in. Introductory Information Form, 'State Anxiety Scale', 'Hemodynamic Variables Monitoring Form' and 'Surgical Fear Scale' will be filled out for all patients who will undergo TURP. Patients in the control group will receive routine care. In the postoperative period, Hemodynamic Variables Monitoring Form, Visual Analog Scale and Discharge Training Satisfaction Scale will be completed for all patients.
Sponsors
Leads: Tarsus University
Collaborators: Necmettin Erbakan University, Mersin University

This content was sourced from clinicaltrials.gov