Effect of Grandmother's Emotional Empowerment of Hospitalized Infants on Anxiety, Depression Symptoms and Maternal Role In Nulliparous Mothers

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2014111013092N4

Enrollment

Registered

2015-03-15

Start date

2014-06-20

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

Disease of pregnancy, childbirth and the puerperium. complications predominantly related to the puerperium

Interventions

Intervention 1: Intervention 2: The control group received routine care. Intervention 2: Intervention 1: In the intervention group, empowering granthmothers in reducing anxiety, depression and increas

Lifestyle

Intervention 2: The control group received routine care

Intervention 1: In the intervention group, empowering granthmothers in reducing anxiety, depression and increased role in nulliparous women according to Mercer's theory and Self management empowerment

Eligibility

Sex/Gender

Female

Age

18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: nulliparous women; age between 18 and 40; health fetus at ultrasonography; without past history of depression in nulliparous women; willingness to participate in the study; literacy; alive and present and willingness to participate in the study of mother's of nulliparous. Exclusion criteria: unwillingness of subjects in any phases of the study; birth defects; still birth; the baby died within a month after admission. Grandmother's inclusion criteria: no particular physical limitations; was retarded and tend to education to her daughter.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Reduce anxiety. Timepoint: The onset of the study and one month after. Method of measurement: Spielberger Anxiety Inventory.;Reduce depression. Timepoint: The onset of the study and one month after. Method of measurement: Beck Depression Inventory.;Improve the quality of role play. Timepoint: The onset of the study and one month after. Method of measurement: Researcher made questionnaire about role plaing.	—

Measure

Time frame

Reduce anxiety. Timepoint: The onset of the study and one month after. Method of measurement: Spielberger Anxiety Inventory.;Reduce depression. Timepoint: The onset of the study and one month after. Method of measurement: Beck Depression Inventory.;Improve the quality of role play. Timepoint: The onset of the study and one month after. Method of measurement: Researcher made questionnaire about role plaing.

—

Secondary

Measure	Time frame
Increase of calmness. Timepoint: The onset of the study and one month after. Method of measurement: Researcher made Questionnaire about Role Playing.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSomaieh Tavasolnia

Deputy for Research- Bushehr University of Medical Sciences

somaieh_tavasolnia@yahoo.com+98 77 3345 0187

Outcome results

None listed

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