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Determining the effect of the implementation of the intervention to make natural childbirth pleasant based on the participation of men

Determining the effect of the implementation of the intervention to make natural childbirth pleasant based on the participation of men

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20231017059753N3
Enrollment
100
Registered
2024-10-31
Start date
2024-11-20
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

Investigating the pleasant effect of natural childbirth on maternal outcomes.

Interventions

Intervention 1: Intervention group: In this study, we have only one intervention group. The intervention group consists of 50 pregnant couples who go to health centers to receive childbirth preparatio

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Consent to participate in the research Primiparous women with low-risk pregnancy single pregnancy. Live and healthy fetus Mother's age is 18-45 years Gestational age 37 to 42 weeks (based on the first day of the last menstrual period or ultrasound of the first trimester) Cephalic presentation8- Normal fetal heart rate (110-160)9- Wives who have been trained in intervention items

Exclusion criteria

Exclusion criteria: History of any incision on the uterus Abnormal bleeding Epidural anesthesia The presence of any abnormalities in the soft or bone tissue of the birth canal Having an abnormal fetus or intrauterine growth restriction Any indication for caesarean section at the time of admission, such as: (fetal distress, prolapse of the umbilical cord, diagnosis of absolute pelvic stenosis by the doctor) Recognized medical diseases based on the patient's file (including history or current suffering from any systemic diseases such as diabetes, high blood pressure, heart disease, kidney disease, nervous disease, liver disease, digestive disease, respiratory disease, thyroid disease)

Design outcomes

Primary

MeasureTime frame
Birth experiencem , Perception of labor pain , Fear of childbirth , Length of labor stages. Timepoint: Checking the results will be 24 to 72 hours after faith. Method of measurement: The results will be measured by different questionnaires. Childbirth Experience Questionnaire (Hosseini et al. 2020), Childbirth Pain Perception Questionnaire (Yadalehi 2016) and Fear of Iman Virjama Questionnaire and a researcher-made questionnaire to measure the length of the stages of labor.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactleila bozorgian

Ahvaz University of Medical Sciences

liela.bozorgian1@gmail.com+98 61 3311 0000

Outcome results

None listed

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