Effectiveness of regular desensitization based on artistic creative simulation compared to behavioral model of ability, opportunity, motivation on fear and pain of childbirth and desire to have children later in first time pregnant women.

Effectiveness of regular desensitization intervention based on artistic creative simulation compared to behavioral model of ability, opportunity, motivation on the fear and pain of childbirth and the desire to have children later in first-time pregnant women

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20240703062315N1

Enrollment

Registered

2024-08-11

Start date

2024-09-10

Completion date

Unknown

Last updated

2024-08-26

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

Conditions

Delivery. Single spontaneous delivery

Interventions

Intervention 1: The first intervention group: The first group received regular desensitization based on artistic creative simulation in 8 online and consecutive sessions, once a week for 90 minutes by

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: Healthy Singleton Pregnancy Gestational Age 20-26 Weeks First Pregnancy Having a Fear of Childbirth Score Equal to or More than 66 Vijma Literacy for Reading and Writing Ability to Speak Persian Willingness to Participate in the Study Having a Smartphone

Exclusion criteria

Exclusion criteria: Fetal/Maternal Disorders Severe life Crises During the last 6 Months Having Mental Disorders Based on the Pregnancy Record

Design outcomes

Primary

Measure	Time frame
Luck / fear of childbirth. Timepoint: Baseline, completion of the intervention in the eighth week and follow-up 24 hours after delivery. Method of measurement: The luck/?Experience of Delivery to Wijma Questionnair.	—

Secondary

Measure	Time frame
Pain. Timepoint: 24 Hours after Delivery. Method of measurement: Visual Pain Scale.;Desire to Have Children. Timepoint: Baseline, completion of the intervention in the eighth week and follow-up 24 hours after delivery. Method of measurement: visual scale of desire to have children.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactTahmineh Farajkhoda

Yazd University of Medical Sciences

farajkhoda_t@yahoo.com+98 35 5117 2438

Outcome results

None listed

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