None listed
Conditions
Brief summary
Patients undergoing diagnostic hysteroscopy for abnormal uterine bleeding will be randomized to intervention or control group. Both groups will complete the State-Trait Anxiety Inventory (STAI-T) before the procedure. The intervention group will then receive a video education and control group will receive verbal information. State-Trait Anxiety Inventory will be repeated following education. Then patients will undergo hysteroscopy in the office setting without anesthesia. Following hysteroscopy, a visual analog scale (VAS) will be responded by the participants to address patients satisfaction. The primary outcome is change in between baseline STAI-T and post-education STAI-T.
Interventions
Demographic data will be obtained before the procedure.
State-Trait Anxiety Inventory scores will be obtained before the procedure and After video education (2 times)
Following the first State-Trait Anxiety Inventory patients allocated to multimedia education will receive approximately 5 minutes of video education concerning demonstration of the procedure. Control group will not receive video education. A 10 years nursing-staff will manage the State-Trait Anxiety Inventory.
Hysteroscopy will be
Demographic data will be obtained before the procedure. State-Trait Anxiety Inventory scores will be obtained before the procedure and After video education (2 times) Following the first State-Trait Anxiety Inventory patients allocated to multimedia education will receive approximately 5 minutes of video education concerning demonstration of the procedure. Control group will not receive video education. A 10 years nursing-staff will manage the State-Trait Anxiety Inventory. Hysteroscopy will be carried out with using a 5.5mm hysteroscope in the office setting without anesthesia. Hysteroscopy will be performed by an 8 years experienced gynecologist (Aysu Akca) Following the procedure, a visual analog scale (VAS) will be applied to subjects to address procedural satisfaction.
Sponsors
Department of Obstetrics and Gynecology, University of Health Sciences, Faculty of Medicine, Kanuni Sultan Suleyman Hospital
Study design
Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Prevention
Masking
Blinded (masking used) (Outcomes Assessor)
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Healthy volunteers
No
Inclusion criteria
Subjects undergoing diagnostic hysteroscopy for abnormal uterine bleeding
Exclusion criteria
psychological disease contraindication for hysteroscopy visual or auditory deficit
Outcome results
None listed