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Empowering Pregnant Woman by a computer based decision aid system

The impact of a computer based gestational hypertension and diabetes decision aids on empowering pregnant women, compared with the conventional care

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013103010777N2
Enrollment
420
Registered
2013-11-07
Start date
2013-11-22
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

Condition 1: Gestational hypertension. Condition 2: Gestational Diabetes. Gestational [pregnancy-induced] hypertension without significant proteinuria Diabetes mellitus arising in pregnancy

Interventions

Intervention 1: Intervention group: they will receive conventional care and a computer based decision aids. Intervention 2: Control group: they will receive the conventional care.
Early detection
Intervention group: they will receive conventional care and a computer based decision aids

Sponsors

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

Eligibility

Sex/Gender
Female
Age
16 Years to 40 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Positive pregnancy test, being in good health, Pregnancy above 18 weeks; Exclusion criteria: inability to read and write and working with computer

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Self efficacy. Timepoint: Before and after of the intervention. Method of measurement: Stanford university, self-efficacy scale.;Knowledge. Timepoint: Before and after of the intervention. Method of measurement: true/false questions.

Secondary

MeasureTime frame
Type and frequency of visiting a doctor. Timepoint: during the intervention. Method of measurement: Data available in the pregnancy records.;Blood pressure and blood sugar. Timepoint: during the intervention. Method of measurement: Data available in the pregnancy records.;Anxiety. Timepoint: before and after of the intervention. Method of measurement: Spielberger anxiety scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohsen Tafaghodi

Mashhad University of Medical Sciences, Vice chancellor for research

tafaghodim@mums.ac.ir+98 511882325566

Outcome results

None listed

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