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Construction and Empirical Study on Mobile Health Support System for Home Care of Premature Infants Based on User Persona

Construction and Empirical Study on Mobile Health Support System for Home Care of Premature Infants Based on User Persona

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300069284
Enrollment
Unknown
Registered
2023-03-12
Start date
2023-03-20
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

premature delivery

Interventions

Intervention group:Intervention for premature infants from the hospital to home based on user persona
Control group:Usual care

Sponsors

Fujian Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. The mediating effect analysis between discharge teaching quality and post-discharge outcomes of premature infants' parents' discharge readiness and parenting competence requires both premature infants and their parents to meet the following inclusion criteria. (1) Premature infants: 1) Gestational age =3d; 3) The parents of premature infants agreed to participate in the study and sign the informed consent. (2) Parents of premature infants: 1) The father/mother who is checking into NICU to treat the premature baby; 2) It is expected to live with premature infants after discharge; 3) As the primary caregiver and medical decision maker for premature infants; 4) Aged >=18 years; 5) No cognitive or mental disorders; 6) Informed consent, voluntarily participate in the study and sign the informed consent. 2. The construction of parent-user portraits for the transition period between hospital for premature infants and families requires both premature infants and their parents to meet the following inclusion criteria. (1) Premature infants: 1) Gestational age =3d; 3) Preterm infants less than 30 days after discharge from the NICU; 4) The parents of premature infants agree to participate in the study and sign the informed consent. (2) Parents of premature infants: 1) Parents of preterm infants within 30 days of discharge from NICU; 2) Live with premature infants after they are discharged from hospital, and the father/mother is the main caregiver of premature infants; 3) Aged >=18 years; 4) No cognitive or mental disorders; 5) Owning a smartphone and having access to the Internet; 6) Informed consent, voluntarily participate in the study and sign the informed consent. 3. The hospital-home transitional mobile medical intervention for premature infants based on user portraits requires both premature infants and their parents to meet the following inclusion criteria. (1) Premature infants: 1) Gestational age =28 weeks; 2) Expected length of stay in NICU >=7d; 3) Guardians of premature infants agree to participate in this study and sign informed consent. (2) Parents of premature infants: 1) Parents of premature infants admitted to NICU; 2) It is expected to live with premature infants after discharge; 3) Parents as primary caregivers and medical decision makers; 4) Aged >=18 years; 5) No cognitive or mental disorders; 6) Owning a smartphone and having access to the Internet; 7) Voluntarily participate in the study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Mediating effect analysis of parents' discharge readiness and parenting competence between discharge teaching quality and outcomes of premature infants after discharge. Premature infants and their parents can be excluded if they meet any of the following exclusion criteria. (1) Premature infants: 1) Premature infants suffer from congenital metabolic diseases and developmental malformations; 2) Triplets and above; 3) Participating in relevant intervention research projects that may change growth and development indicators. (2) Parents of premature infants: (1) The mother has serious obstetric complications/complications or other critical diseases caused by non-obstetric factors; 2) The parent has serious audio-visual impairment, which may affect his/her understanding of the question or correct response; 3) Parents are participating in other intervention studies that can change their readiness to leave the hospital, their sense of competence in parenting, and their ability to care. 2. For the construction of parent-user portraits in transitional period between hospital for premature infants and families, premature infants and their parents can be excluded if they meet any of the following exclusion criteria. (1) Premature infants: 1) Premature infants suffer from congenital metabolic diseases and developmental malformations; 2) Triplets and above. (2) Parents of premature infants: 1) The mother of a preterm infant has severe obstetric complications/complications or other major diseases caused by non-obstetric factors; 2) The parent has a serious audio-visual impairment, which may affect the understanding of the question or the correct response; 3) Parents are participating in research interventions that may affect caregiving, parenting competence, and e-health literacy. 3. For hospital-family transitional mobile medical intervention for premature infants based on user portraits, premature infants and their parents can be excluded if they meet any of the following exclusion criteria. (1) Premature infants: 1) Premature infants suffer from congenital metabolic diseases and developmental malformations; 2) Triplets and above; 3) Participating in relevant intervention studies that may change follow-up outcomes. (2) Parents of premature infants: 1) The mother of a preterm infant has severe obstetric complications/complications or other major diseases caused by non-obstetric factors; 2) The parents have serious audio-visual impairment, which may affect the understanding of the question or the correct response; 3) Parents are participating in other intervention studies that may change hospital discharge readiness, parenting competence, and caregiving ability.

Design outcomes

Primary

MeasureTime frame
Premature infant care competence for parents in transition;E-health literacy for parents;

Secondary

MeasureTime frame
The quality of discharge teaching;The parental readiness for hospital discharge;Parenting sense of competence;Weight of premature infants;Height of premature infants;Head circumference of premature infants;Number of unplanned readmissions of preterm infants within 30 days of discharge;Emergency room visits of preterm infants within 30 days of discharge;Depression, anxiety, stress;The Neonatal Behavioral Neurological Assessment;General demographic data of premature infants and parents;Number of unplanned readmissions of preterm infants within 90 days of discharge;Emergency room visits of preterm infants within 90 days of discharge;

Countries

China

Contacts

Public ContactWang Xiaojuan

Fujian Medical University

nydwxj@163.com+86 18109579016

Outcome results

None listed

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