Development and Evaluation of an Intelligent Parent-Infant Connection-Based Intervention to Strengthen Family Resilience in Preterm Infant Care
Starting soon · Not applicable
Conditions studied: Family Resilience, Parent-Infant Bonding, Parents of Premature Infants, Intelligent Intervention
In brief
This study aims to develop, optimize, and evaluate the effectiveness of a family resilience intervention centered on intelligent parent-infant connection for parents of preterm infants. Using a longitudinal randomized controlled trial design, it examines the intervention's impact on parental psychosocial health, parenting efficacy, family resilience, and parent-infant interaction from NICU hospitalization to six months post-discharge.
Key facts
- Study ID
- NCT07373002
- Run by
- National Defense Medical Center, Taiwan
- People needed
- 300
- Starts
- 2026-08-01
- Expected to finish
- 2029-07-31
- Last updated by the study team
- 2026-07-09
Who can join
Age: 18 and older, up to 80. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- The infant is born prematurely with a gestational age of less than 37 weeks.
- At least one parent of the premature infant is aged 18 years or older and can communicate in Mandarin or Taiwanese.
- The parent(s) have provided informed consent to participate in the study.
- The parent(s) are able to comply with the data collection procedures (participation of both parents is encouraged but not required).
You may not qualify if…
- The premature infant has major congenital anomalies or is assessed by clinicians as unlikely to survive.
- The parent(s) are unable to use a smartphone or internet-connected device due to technical, cognitive, or other limitations.
- The parent(s) have a known history of severe psychiatric disorders, intellectual disabilities, or substance abuse, and are assessed by the research team as being unable to comply with the study procedures or intervention requirements.
Full record on ClinicalTrials.gov
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