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Evaluation of the effectiveness of prenatal self-care training application in Covid 19 pandemic on quality of life, depression, corona anxiety and fear of childbirth in pregnant women

Evaluation of the effectiveness of prenatal self-care training application in Covid 19 pandemic on quality of life, depression, corona anxiety and fear of childbirth in pregnant women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210531051457N1
Enrollment
80
Registered
2021-06-27
Start date
2021-06-22
Completion date
Unknown
Last updated
2021-07-12

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

Conditions

Condition 1: Depression. Condition 2: Quality of Life. Condition 3: Corona anxiety. Condition 4: Fear of childbirth.

Interventions

Intervention 1: Intervention group: Pregnancy self-care application, which is designed according to the instructions of the Ministry of Health during pregnancy, and is very comprehensive, is provided

Sponsors

Gonabad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 49 Years

Inclusion criteria

Inclusion criteria: Gestational age less than 20 weeks maternal age 15-49 years informed consent to participate in research after hearing research goals and programs Internet access and messengers possibility of making telephone calls to pregnant mother first or second pregnancy, Having literacy in Persian waned pregnancy not having any physical or mental illnesses according to the mother not having a fetus with abnormalities not getting a high score of anxiety or depression from the questionnaires not having a history of infertility Having a smartphone

Exclusion criteria

Exclusion criteria: Failure to receive and perform training failure to complete questionnaires at any stage of the research abortion major stress during the intervention such as death of a relative person or spouse or child with corona heart disease

Design outcomes

Primary

MeasureTime frame
Quality of life score in two groups. Timepoint: At the beginning of the intervention and immediately after the end of the study. Method of measurement: Global Health Quality of Life Standard Questionnaire sf-36.;Depression score. Timepoint: At the beginning of the intervention and immediately after the end of the study. Method of measurement: Depression Questionnaire dass-21.;Corona Anxiety Score. Timepoint: At the beginning of the intervention and immediately after the end of the study. Method of measurement: Corona Anxiety Questionnaire Ahmad Alipour.;Fear of childbirth score. Timepoint: At the beginning of the intervention and immediately after the end of the study. Method of measurement: Harman Maternity Fear Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRoghaieh Rahmany

Gonabad University of Medical Sciences

roghaiehrahnany@yahoo.com+98 51 5722 3028

Outcome results

None listed

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