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Comparison of effect of group and individual Education on informed choice of pregnant women about screening tests of fetal chromosomal disorders

Comparison of effect of group and individual Education on informed choice of pregnant women about screening tests of fetal chromosomal disorders

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014081318785N1
Enrollment
240
Registered
2015-08-03
Start date
2014-08-23
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

Antenatal Screening. Routine Prenatal Care

Interventions

Intervention 1: control group: the usual care was conducted in two consecutive weeks. Intervention 2: Intervention group 1: In the individual education, screening and diagnostic information Will be pr
Behavior
control group: the usual care was conducted in two consecutive weeks.
Intervention group 1: In the individual education, screening and diagnostic information Will be presented to face to face method in during two sessions of 45 to 60 minutes and in two consecutive weeks
Intervention group 2: In the group education, screening and diagnostic information Will be presented to lecture method in during two sessions of 45 to 60 minutes and in two consecutive weeks.

Sponsors

Vice chancellor for research, Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria: Muslim and Iranian; Consent to participate in research; Gestational age less than 10 weeks; Have at least five elementary education; Having full consciousness and the ability to receive auditory and speech training and answer questions; Lack of indication for diagnostic tests; Not being a member of the health team. Exclusion criteria: Absence in one of the training sessions; Leave the class before the end of training; Lack of The desire to continue participating in the study; Fetal death during the study; Occurring unpleasant events during training sessions.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Informed Choice. Timepoint: Before Intervention and Three Months after Intervention. Method of measurement: Informed Choic Scale.

Secondary

MeasureTime frame
Worry. Timepoint: Before Intervention and Three Months after Intervention. Method of measurement: Cambridge Worry Questionnaire.;Anxiety. Timepoint: Before Intervention and Three Months after Intervention. Method of measurement: Spielberger Questionnaire.;Decisional Conflict. Timepoint: Before Intervention and Three Months after Intervention. Method of measurement: Decisional Conflict Questionnaire.;Well Being. Timepoint: Before Intervention and Three Months after Intervention. Method of measurement: WHO-5-Well Being Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSahar Riyazi

Mashhad University of Medical Sciences

riyaziz911@mums.ac.ir+98 51 3270 9157

Outcome results

None listed

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