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Clinical Trials in Turkey / NCT06616090
Starting soon Not applicable

Nurse Implemented Infant-Mother Attachment Security Program

NCT06616090 · tracked via the Priya Life Science Turkey tracker
Sponsor
Sabanci University
Phase
Not applicable
Started
2024-10-01
Last updated
2024-09-27

Condition(s) studied

Nurse's RoleInfant DevelopmentMaternal Behavior

Investigational drug(s) / intervention(s)

Nurse Implemented Infant-Mother Attachment Security Program

Nurse Implemented Infant-Mother Attachment Security Program: The intervention will draw on video-feedback of mother-infant interactions during the well-child visit. Nurses will videotape the dyad during routine visit in the Family Health Center and show short clips to mothers during the session in order to provide mother positive feedback on their sensitive caregiving. Additionaly, intervention mothers will be exposed to the reminders (e.g., pictures, posters, short film screenings) reflecting maternal sensitivity and secure attachment in the waiting rooms of the intervention Family Health Centers.

Study summary

This study focuses on adapting and evaluating an attachment-based intervention program implemented by nurses in Family Health Centers (FHCs) in Turkey. The program aims to enhance parental sensitivity and infant-mother attachment security. Evidence suggests that such programs, developed in Western countries, effectively improve parenting behaviors and attachment quality. Despite the positive effects of similar programs in Turkey, their integration into primary healthcare for wider public benefit remains unexplored. The project will develop an intervention protocol based on effective methods from previous attachment-based programs into routine childcare visits at FHCs. A randomized controlled trial involving 120 mothers with 9- to 12-month-old babies in Istanbul will be recruited. FHCs will be randomly assigned to intervention and control groups, with 60 mother-infant dyads in each condition. Nurses will deliver the program during childcare visits at 9, 12, 15, and 18 months. Intervention FHCs will also use reminders like posters and short films in the waiting rooms to reinforce the concepts. Effectiveness will be evaluated through pretest, posttest, and follow-up home visits using observational and self-report measures on attachment security, maternal sensitivity, as well as maternal psychological characteristics, along with infant socioemotional measures. Upon completion of the project, control FHC nurses will receive training to deliver a condensed version of the program.

Eligibility

Sex
FEMALE
Min age
—
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * mothers with 9- to 12-month infants * having a normally developing infant. Exclusion Criteria: * mothers with infants who have a chronic pediatric health problem * mother with infants whose developmental problems are detected during routine evaluations * mothers with temporary protection status (i.e., immigrants) due to potential communication problems * if the mother is not the primary caregiver

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Sabanci University Istanbul Turkey (Türkiye)

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06616090 on ClinicalTrials.gov ↗ ← All trials in Turkey