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The effect of home visit educational program on prematur infant's mothers anxiety

Assessment of the effect of home visit educational program on prematur infant's mothers anxiety

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180729040621N1
Enrollment
70
Registered
2018-12-02
Start date
2018-08-23
Completion date
Unknown
Last updated
2019-01-14

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

Conditions

Mothers anxiety. Psychotic disorder with hallucinations due to known physiological condition

Interventions

Intervention 1: Intervention group:Educational program. Intervention 2: Control group: Group without educational program.

Sponsors

Babol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: The preterm infants with 28-37 weeks of gestation The preterm infants without brain disorders, Congenital heart diseases, Metabolic or endocrine diseases,Known genetic and chromosomal disorders and intraventricular hemorrhage Not having a previous experience of the hospitalized infant in NICU or the death Lack of stressful events at the time of intervention in the family including no separation and no death of first-degree relatives in the past six months The mother is not a member of the healthcare team.

Exclusion criteria

Exclusion criteria: The preterm infants with congenital anomalies and nervous system The parents have other children with serious illness Experience of the hospitalized infant in NICU or the death of infant Presence of stressful events at the time of intervention in the family such divorcement or as losing the job,or death of first-degree relatives in the past six months The parents cannot read and write in Persian The mother uses the anxiolytics and has the history of drug addiction.

Design outcomes

Primary

MeasureTime frame
Anxiety. Timepoint: At the beginning of the study (before the intervention),after 2 sessions and 4 weeks after the last training session in the intervention group. Method of measurement: Spielberger STAI.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactParvin Aziznejadroshan

Babol University of Medical Sciences

aziznejadroshan@yahoo.com+98 11 3219 9592

Outcome results

None listed

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