Skip to content

Virtual Solution-Based Counseling in Fear of Delivery, Anxiety and Depression of Pregnant Women

The Effect of Virtual Solutions - Focused Counseling on the Fear of Delivery, Anxiety and Depression of Pregnant Women

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190609043848N1
Enrollment
168
Registered
2020-07-28
Start date
2020-01-20
Completion date
Unknown
Last updated
2020-08-17

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

Conditions

Condition 1: Fear of Childbirth. Condition 2: Pregnancy Anxiety. Condition 3: Depression Pregnancy.

Interventions

Intervention 1: Intervention group: First, the consent of pregnant women to participate in the research will be obtained. If satisfied, the Demographic and Expectancy / Childbirth Questionnaire (W-DEQ
Session 2 (Week 31): Measuring and identifying a person's strengths and abilities
Session 3 (Week 32): Summarize the previous session and examine the problems, goals and how to achieve them through the use of the technique of exceptions and miracle questions, and finally the emphas

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Primiparous women and multiparous women without history of cesarean section with a score assigned at the cut-off point of fear, anxiety and depression scales. Ages 18-35. within the week of 28-30 weeks of pregnancy. Pregnant women with no indication of high-risk pregnancy. Lack of medical indications for cesarean section. Having no mental health problems or mental or physical disabilities that prevent us from answering questions. Access from an Android-powered smartphone or tablet.

Exclusion criteria

Exclusion criteria: Pregnant mother lacks access to software Not willing to cooperate at any stage of the study Any mental problems the medication uses Not using application in virtual consulting group for 2 weeks

Design outcomes

Primary

MeasureTime frame
Fear of Childbirth. Timepoint: Before the intervention and at the end of the sixth week of the intervention. Method of measurement: Wijma Delivery Expectancy/Experience Questionnaire(W-DEQ version A ).;Pregnancy Anxiety. Timepoint: Before the intervention and at the end of the sixth week of the intervention. Method of measurement: Depression Anxiety Stress Scales (DASS).;Pregnancy Depression. Timepoint: Before the intervention and at the end of the sixth week of the intervention. Method of measurement: Depression Anxiety Stress Scales (DASS).

Secondary

MeasureTime frame
Select the type of delivery. Timepoint: Before the intervention and at the end of the sixth week of the intervention. Method of measurement: one question.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMarzieh Rezaeiaref

Iran University of Medical Sciences

rezaeearef.m@iums.ac.ir+98 25 3240 8024

Outcome results

None listed

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