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The Effect of Using a Childbirth Preparation Mobile Application on Spousal Social Support among Pregnant Women and Their Husbands

Effect of App-Based Childbirth Preparation Education in Pregnant Women and Their Husbands on Spousal Social Support: A Randomized Controlled Clinical Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20110827007422N9
Enrollment
64
Registered
2026-05-23
Start date
2026-06-22
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Spousal social support.

Interventions

Intervention 1: Intervention Group: In this study, the intervention group will consist of pregnant women and their spouses. Participants in the intervention group will receive the educational program

Sponsors

Mazandaran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 49 Years

Inclusion criteria

Inclusion criteria: Primiparous women between 20 and 30 weeks of gestation who are willing to participate in the study Singleton, low-risk pregnancy without complications Ability to read and write in order to use the application content, with availability for contact and follow-up No previous participation in childbirth preparation classes Women aged 15 to 49 years No history of infertility, miscarriage, or stillbirth First marriage Ownership of a smartphone capable of installing and using the application Inclusion criteria for men (husbands):Men who are willing to participate in the study Ability to read and write in order to use the application content, with availability for contact and follow-up Ownership of a smartphone capable of installing and using the application No previous experience of fatherhood First marriage

Exclusion criteria

Exclusion criteria: Presence of chronic diseases (such as diabetes, renal diseases, cardiovascular diseases, chronic hypertension, etc.) Presence of known neurological or psychiatric disorders, based on the mother’s self-report or a positive initial mental health screening conducted by health centers Use of psychoactive substances, cigarettes, or alcohol Occurrence of any adverse event during the study period Failure to use the application for two consecutive weeks

Design outcomes

Primary

MeasureTime frame
Spousal Social Support. Timepoint: Before the intervention - Immediately after the intervention - 4 weeks after the end of the intervention. Method of measurement: Scale of Sherborne and Stewart social support.

Secondary

MeasureTime frame
Pregnancy experience. Timepoint: Before the intervention - Immediately after the intervention - 4 weeks after the end of the intervention. Method of measurement: Short version of the pregnancy experience scale.;Satisfaction with the training method. Timepoint: Immediately after the intervention - 4 weeks after the end of the intervention. Method of measurement: Satisfaction questionnaire on how to conduct maternity classes.;Self-assessment related to education (knowledge). Timepoint: Before the intervention - Immediately after the intervention - 4 weeks after the end of the intervention. Method of measurement: Self-assessment questionnaire created by the researcher.;Self-efficacy. Timepoint: Before the intervention - Immediately after the intervention - 4 weeks after the end of the intervention. Method of measurement: General self-efficacy questionnaire (GSE-10).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaral Lotfi

Mazandaran University of Medical Sciences

lotfimararl76@gmail.com+98 11 3336 7344

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Jun 11, 2026