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Design and implementation of interventions to improve unplanned pregnancy experiences

Design and implementation of interventions to improve unplanned pregnancy experiences

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170506033834N12
Enrollment
60
Registered
2024-02-12
Start date
2024-06-21
Completion date
Unknown
Last updated
2024-03-06

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

Conditions

pregnancy.

Interventions

Intervention 1: Intervention group:The target population will be women aged 18 to 45 with an unplanned pregnancy who refer to Tabriz city health centers for prenatal care in 1403. In this step, sampli

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Women with unplanned pregnancies Mother's age is 18-45 years singleton pregnancy Live fetus

Exclusion criteria

Exclusion criteria: Vaginal bleeding (threat of miscarriage) Previous history of depression according to mother's statement Having maternal or fetal indications for termination of pregnancy Disagreement with the wife according to mother's statement

Design outcomes

Primary

MeasureTime frame
Pregnancy experiences. Timepoint: before the start of the intervention and again after the intervention in the 35th to 37th week of pregnancy with control of the baseline effect. Method of measurement: PES (Pregnancy Experience Scale) Questionnaire.

Secondary

MeasureTime frame
Mother's anxiety. Timepoint: before the start of the intervention and again after the intervention in the 35th to 37th week of pregnancy by controlling the effect of the baseline score. Method of measurement: PRAQ (Pregnancy-Related Anxiety Questionnaire).;Depression. Timepoint: before the start of the intervention and again after the intervention in the 35th to 37th week of pregnancy by controlling the effect of the baseline score. Method of measurement: Edinburgh's Depression During Pregnancy Tool.;Perceived maternal violence. Timepoint: before the start of the intervention and again after the intervention in the 35th to 37th week of pregnancy with control of the baseline effect. Method of measurement: 4-item tool HITS (Hurts, Insults, Threaten, Screams).;Mother's attachment to the fetus. Timepoint: before the start of the intervention and again after the intervention in the 35th to 37th week of pregnancy with control of the baseline effect. Method of measurement: Cranley's mother-fetus attachment questionnaire.;Preterm delivery. Timepoint: Frequency of preterm delivery with effect adjustment of baseline values. Method of measurement: Baby care card.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMasoumeh Paiandeh

Tabriz University of Medical Sciences

m_paiande@yahoo.com+98 41 6770 3479

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 5, 2026