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Design and Validation of a Mobile Self-Care Application on the Quality of Life of Primiparous Women

Design and Validation of a Mobile Self-Care Application on the Quality of Life of Primiparous Women After Childbirth

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250610066160N1
Enrollment
110
Registered
2025-06-17
Start date
2025-07-16
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Postpartum Primiparous Women. Encounter for routine postpartum follow-up

Interventions

Intervention 1: Intervention group: The intervention will be such that the participants in the intervention group, in addition to routine and usual training and care, will use the relevant application

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Primiparous women Absence of severe postpartum depression based on the Edinburgh Postpartum Depression Scale (score less than 13) Ages 20 to 40 No underlying diseases Childbirth without complications Having a healthy baby Being able to read and write in Persian Having an Android mobile phone and being able to work with it Absence of hearing, tactile, visual, and speech disorders

Exclusion criteria

Exclusion criteria: Hospitalization of the baby or mother An unfortunate incident occurs. Using the app for less than 1 hour during the research period Having a sick or disabled child

Design outcomes

Primary

MeasureTime frame
Quality of life. Timepoint: Quality of life measurement at the beginning of the study (before the start of the intervention) and 6 weeks after the start of the intervention. Method of measurement: Postpartum Women's Quality of Life Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRaheleh Babazadeh

Mashhad University of Medical Sciences

babazadehr@mums.ac.ir+98 51 3884 6730

Outcome results

None listed

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