The Effect of Using Multimedia During the Informed Consent Process on the Anxiety of Parents of Orchiopexy Patients
Recruiting · NCT06698081 · Interventional (participants receive a specific treatment)
View the official record on ClinicalTrials.gov →Interventions studied
Video Multimedia
What this trial is about
Aim: The goal of this randomized controlled trial is to detect the effect of using multimedia during the informed consent process on the anxiety of parents of orchiopexy patients. Parents (primary caregivers) of the patients who underwent orchiopexy surgery are included in the study. The main question it aims to answer is: • Does the use of multimedia during the preoperative consent process affect the anxiety level of parents of patients undergoing orchiopexy surgery?
Who can take part
Age range
18 Years and older
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
Inclusion criteria
- parents of orchiopexy patients
Exclusion criteria
- history of previous orchiopexy surgery
- orchiopexy with other surgical procedures ( f.e. Hypospadias repair)
Where it is running
1 location listed.
- Marmara University School of Medicine, Department of Urology - Istanbul, Istanbul, Turkey (Türkiye)