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The effect of Midwifery Consultation on Prenatal Grief

Comparison of The Effect of Midwifery Consultation With Existential Approach and routine care On Prenatal Grief in mothers with pregnancy loss: a clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017082424339N1
Enrollment
100
Registered
2017-10-19
Start date
2016-08-13
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

Psychological support in pregnancy. pregnancy-related condition unspecified

Interventions

Intervention 1: Control group: The control group will receive routine care. Intervention 2: Intervention group: The intervention group will participate in existential sessions (6sessions,45-60 minutes
Behavior
Control group: The control group will receive routine care.
Intervention group: The intervention group will participate in existential sessions (6sessions,45-60 minutes) as well as receiving routine care.

Sponsors

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

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: presence of abortion, ectopic pregnancy, moles, stillbirth; at least junior high-school education; no depression background, psychological disorders or physical ailments; no participation in other medical programs; not receiving individual consultation or medication; informed consent to participate in the study. Exclusion criteria: elective abortion; unmarried individuals; under 18 individuals, drug abuse.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Complicated Grif. Timepoint: Before the intervention, six weeks later, three months later. Method of measurement: Standard questionnaire of prenatal grief.

Secondary

MeasureTime frame
Depression. Timepoint: Before the intervention, six weeks later, three months later. Method of measurement: Standard questionnaire of Wijma Delivery Expectancy/Experience(W-DEQ).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSoheila Mirzabeigi

Shahroud University Of Medical Sciences

Mirzabeigi.so@gmail.com+98 2732332394499

Outcome results

None listed

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