Normal vaginal delivery. Encounter for full-term uncomplicated delivery
Conditions
Interventions
Intervention 1: Intervention group 1: Pregnant women who were candidate for first vaginal delivery and had a good hypnotizability were recruited to hypnosis group. Pregnant mothers were trained for hy
Sponsors
Mashhad University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Pregnant women who are candidate for the first vaginal delivery Pregnant women who had good hypnotic induction profile
Exclusion criteria
Exclusion criteria: History of gestational diabetes History of intrauterine growth restriction (IUGR) History of any comorbidities in current pregnancy History of previous vaginal delivery Use of neuraxial blocking agents during delivery
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Labor pain. Timepoint: Immediately after delivery. Method of measurement: Visual Analogue Scale. | — |
Secondary
| Measure | Time frame |
|---|---|
| State and trait anxiety. Timepoint: One month after delivery. Method of measurement: Spielberger State-Trait Anxiety questionnaire.;Post-partum depression. Timepoint: One month after delivery. Method of measurement: Edinburgh Postnatal Depression Scale.;Fear of delivery. Timepoint: Immediately after delivery. Method of measurement: Visual Analogue Scale.;Delivery method satisfaction. Timepoint: Immediately after delivery. Method of measurement: Visual Analogue Scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMehdi Fathi
Mashhad University of Medical Sciences
Outcome results
None listed