Female infertility. Female infertility of tubal origin
Conditions
Interventions
Intervention 1: Control group: Control group: After accepting people according to the entry criteria, and obtaining informed consent, people are randomly assigned to the control and intervention group
Sponsors
Tarbiat Modares University
Eligibility
Sex/Gender
Female
Age
20 Years to 49 Years
Inclusion criteria
Inclusion criteria: Voluntary infertile women Age 20-49 years Iranian nationality Ability to speak Persian Literacy Not suffering from known anxiety disorders or other mental illnesses affecting anxiety under treatment No history of HSG People who are inclined to participate in the study.
Exclusion criteria
Exclusion criteria: Patient withdrawal from the study Failure to complete the HSG process for any reason Presence of tubal or uterine lesions, such as cervical stenosis, which cause "severe pain" in the HSG process
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The patient's heart rate. Timepoint: Heart rate measurement at the beginning of the study (before the intervention), half an hour before the intervention, immediately and half an hour after the intervention. Method of measurement: Pulse meter.;The patient's blood pressure. Timepoint: Blood pressure measurement at the beginning of the study (before the intervention), half an hour before the intervention, immediately and half an hour after the intervention. Method of measurement: Sphygmomanometer.;Patients' awareness of hysterosalpingography. Timepoint: Measuring the patient's knowledge about hysterosalpingography at the beginning of the study (before the intervention), half an hour before the intervention, immediately and half an hour after the intervention. Method of measurement: Hysterosalpingography awareness questionnaire (made by a researcher).;Patient anxiety. Timepoint: Measuring the patient's anxiety at the beginning of the study (before the intervention), half an hour before the intervention, immediately and half an hour after the intervention. Method of measurement: State Trait Anxiety Inventory (STAI).;Perceived pain from the hysterosalpingography procedure. Timepoint: Measurement of perceived pain in the initial study (before the intervention), half an hour before the intervention, treatment and half an hour after the intervention. Method of measurement: Visual analog scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactShahideh Jahanian Sadatmahalleh
Tarbiat Modares University
Outcome results
None listed