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The effect of midwifery led counseling on childbirth fear and self-efficacy

The effect of midwifery led counseling based on gamble's Approach on childbirth fear and self-efficacy in nulligravida women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20101219005417N3
Enrollment
80
Registered
2018-12-19
Start date
2018-07-06
Completion date
Unknown
Last updated
2019-01-14

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

Conditions

The fear of childbirth and self-efficacy for pregnant women.

Interventions

Intervention 1: Control Group: This group will receive their special standard care. Intervention 2: Intervention group: Based on Gamble`s approach, two midwifery- based counseling sessions will be pre

Sponsors

Zanjan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Age 18-35 years old The first pregnancy Monogamous fetus There is no history of infertility Not having a history of chronic illness, medical or obstetrical The lack of a history of mental health disorders and taking psychedelic drugs The desire to participate in the study Having at least cycle education Earning a score equal to or higher than 66 wijma fear questionnaire Earning a score of less than or equal to the 51 of Toronto's questionnaire The current mental health score the mother include lack of depression less or equal to 13; anxiety score less than or equal 9; lack of stress less than or equal to 18

Exclusion criteria

Exclusion criteria: Fetal death before birth in the domain of research time Ultrasound of the abnormal embryo

Design outcomes

Primary

MeasureTime frame
- nulligravida women`s childbirth fear. Timepoint: 20-24 weeks of pregnancy (before starting the intervention) and twelve weeks after the start of the intervention. Method of measurement: Wijma fear questionnaire (Version A W-DEQ).;Nulligravida women`s self- efficacy. Timepoint: Twenty-four weeks of pregnancy (before the start of the intervention) and twelve weeks after the start of the intervention. Method of measurement: The questionnaire and the scale of the expected outcome of the delivery and efficacy of Louie.

Secondary

MeasureTime frame
The preferred method of delivery. Timepoint: Twenty four weeks of pregnancy (before the start of the intervention) And thirty-six weeks of pregnancy. Method of measurement: The preferred method of delivery of the questionnaire a question.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactLaya Firouzan

Zanjan University of Medical Sciences

l.firouzan6008@gmail.com+98 24 3314 8375

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 17, 2026