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Development and evaluation of an APP for maternal and child health management

Development and evaluation of an APP for maternal and child health management

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300072729
Enrollment
Unknown
Registered
2023-06-22
Start date
2023-06-20
Completion date
Unknown
Last updated
2023-06-26

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

Conditions

Maternal and child health

Interventions

Intervention group:Mobile health management platform for maternal and child
Control group:Routine Care

Sponsors

Xiangya School of Public Health, Central South University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: (1) Women and their family members: This includes women between the ages of 18 and 45 who are visiting the research site for medical treatment. Additionally, their family members are also included in this group. (2) Healthcare personnel: This group comprises healthcare professionals working in healthcare facilities such as maternal and child health hospitals, community health service centers, and township health centers. Inclusion criteria for participants of maternal mental health management program: women between the ages of 18 and 45 who are visiting the research site for healthcare.

Exclusion criteria

Exclusion criteria: Individuals who have a previous history of mental illness or who are currently experiencing acute or chronic diseases, as well as those with communication disorders that hinder their ability to independently complete the investigation or actively participate in the research, would be excluded from the study. Exclusion criteria for participants of maternal mental health management program: Individuals who have a previous history of mental illness or who are currently experiencing acute or chronic diseases, as well as those with communication disorders that hinder their ability to independently complete the investigation or actively participate in the research.

Design outcomes

Primary

MeasureTime frame
Sense of efficacy;Depression;Anxiety;sleep quality;Social support;

Secondary

MeasureTime frame
marital quality;Parenting efficacy;Intervention acceptance;Feasibility of intervention;Satisfaction of intervention;Usefulness of intervention;

Countries

China

Contacts

Public ContactWenjie Gong

Central South University

gongwenjie@csu.edu.cn+86 136 0744 5252

Outcome results

None listed

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