Skip to content

The effect of group discussion between mothers and caregivers team about premature neonate on their stress and coping in Neonatal Intensive Care Unit

The effect of group discussion between mothers and caregivers team about premature neonate on their stress and coping in Neonatal Intensive Care Unit

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016120631262N1
Enrollment
80
Registered
2017-03-10
Start date
2017-02-19
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

stress and coping. Neurotic, stress-related and somatoform disorders

Interventions

Intervention 1: control group: mothers who have signed a written informed consent and filled demographic data form, Parental Stress Scale and The Brief Cope questionnaire in the first three days of ad
after the last session mothers will fill parenting stress and The Brief Cope questionnaire.
Behavior
control group: mothers who have signed a written informed consent and filled demographic data form, Parental Stress Scale and The Brief Cope questionnaire in the first three days of admission and agai
Intervention group: intervention group: after necessary explanations about study aims to mothers, and filling written contest, in first three days of admission, demographic data form, Parental Stress

Sponsors

Vice chancellor for Research Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: : inclusion criteria consisted of mothers with infants hospitalized in neonatal intensive care unit at gestational age less than 35 weeks. Mothers' willingness to participate in the study, no history of mental illness and use of psychotropic drugs, the ability to understand and read in Persian, no previous premature infants, and risk of hospitalization for more than two weeks. Exclusion criteria included surgical complications for infants, or not participating in two of four meeting or the baby death.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Stress. Timepoint: in the first three days of admission and again two weeks later. Method of measurement: PSS:NICU.;Coping. Timepoint: in the first three days of admission and again two weeks later. Method of measurement: The Brief Cope.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactJila Mirlashari

School of Nursing and Midwifery, Tehran University of Medical Sciences

jmirlashari@yahoo.com+98 21 6692 7171

Outcome results

None listed

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