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Antenatal classes on pregnancy anxiety, desensitization integration in nulliparous women

Clinical trial comparing the effectiveness of desensitization integration in preparation for childbirth classes to pregnant women anxiety that participate in regular classes in preparation for childbirth

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016060428240N1
Enrollment
76
Registered
2016-06-16
Start date
2016-06-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Anxiety. Other anxiety disorders

Interventions

Intervention 1: In the intervention group, in addition to previous training in preparation for childbirth classes given Desensitization in the course of the fifth to the eighth session done. Intervent
Behavior
In the intervention group, in addition to previous training in preparation for childbirth classes given Desensitization in the course of the fifth to the eighth session done.
In the control group of mothers in childbirth preparation classes according to their past.

Sponsors

Vice Chancellor for research; Shahroud University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria consisted of: Causing the first being about 20 weeks gestational age, age between 20 and 35 years, the same anxiety (Business forget of 20 to 69 in Scale anxiety, including anxiety is mild to moderately severe), lack of medical-surgical diseases ( Blood pressure, diabetes),No history of psychiatric or mental illness, and the normal healthy fetus in the first trimester graphic examination (without any fetal abnormalities, the normal location of the placenta, normal cervical length)?No apparent obstacles for normal delivery at the time of sampling, any contraindications to vaginal delivery, having the symptoms of threatened abortion, have at least read and write, singleton pregnancy, non-smoking, drugs and alcohol, single spouse, Lack of recurrent miscarriage and infertility. Exclusion criteria: absence of more than two sessions, moved, and the unavailability of pregnant women and pregnancy termination for any reason before the end of counseling, the creation of any indication for cesarean delivery.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Anxiety. Timepoint: Before intervention? 4 months after treatment. Method of measurement: Spielberger questionnaire.

Secondary

MeasureTime frame
Behavior change. Timepoint: Before intervention?Delivery time. Method of measurement: Information delivery.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFateme yaghoobi moghadam bilondi

Shahroud university of medical sciences

f.yaghoobi.m@gmail.com;yaghoobi@shmu.ac.ir+98 51 5733 2689

Outcome results

None listed

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