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Comparison of theAccompanying Midwife with Non-Obstetrician at Birth

Comparison of the Effect of Accompanying Midwife and Non-Midwife on the degree of Aanxiety and Labor Pain in Primipara Women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20171111037380N1
Enrollment
120
Registered
2018-09-11
Start date
2017-11-16
Completion date
Unknown
Last updated
2018-10-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Condition 1: Anxiety. Condition 2: Labor Pain. Mental disorders and diseases of the nervous system complicating pregnancy, childbirth and the puerperium -Complications of labour and delivery

Interventions

Intervention 1: Intervention group 1: Intervention group 1 with Midwife. In this group, a Midwife who has completed a Physiological Delivery and is a member of the Midwifery Counseling and Counseling

Sponsors

Qazvin University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 40 Years

Inclusion criteria

Inclusion criteria: Iranian Native-Born Women Sunnis 15-40 Years Old The Pregnancy is between 37 Weeks and 42 Weeks Have a Live Embryo, Monocular and without major Anomalies Cephalic display and Normal weight 4000- 2500 Presence of Labor Contractions, Dilatation 3-4 cm, proper Pelvic Position

Exclusion criteria

Exclusion criteria: - The Presence of Acute and Chronic Psychiatric Neuropsychiatric and Anxiety Recorded in the case and use of a Special Psychic disorder - Having a History of Acute and Chronic Pain, such as Migraine and Appendix, etc. Recorded in the case Having an Indication of Cesarean Section such as history of Surgery on the Uterus, Placenta Pervia, Head and Pelvic Misalignment, Preeclampsia, Cervicellacae Cervix, Fetal Distress and Partial ?Early Retirement Use of Analgesic in the last 8 hours - History of Blood Pressure, Gestational Diabetes and Other Underlying Illnesses Recorded in the case - History of Alcohol Addiction, Smoking and Drug use - Unwilling to Participate in Research

Design outcomes

Primary

MeasureTime frame
Improve Satisfaction. Timepoint: At the end of the Intervention. Method of measurement: Checklist.;Duration of the Active Phase First and Second Stages of Labor. Timepoint: From the onset of the Active Phase (3-4 cent) to Baby Delivery. Method of measurement: Partograph.

Secondary

MeasureTime frame
Anxiety. Timepoint: Before Entering the Study, After Entering the Study in Dilatation 3-4, 8-10 and Postpartum. Method of measurement: Spilberger's Explicit and Secret Anxiety Questionnaire.;Labuor Pain. Timepoint: Before Entering the Study, After Entering the Study in 3-4 centuries Dilatation, 5-7 cm and the Second Stage of Labor. Method of measurement: Visual Analogue Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Zainat Jorabchi

Qazvin University of Medical Sciences

zjourabchi@yahoo.com+98 28 3333 6001

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026