normal delivery,cesarean section
Conditions
Interventions
Experiemntal group:Patients In the intervention group completed the pre-control forms everyday.
Control group:Patients in the control group completed the pre-control forms when they were discharged.
Sponsors
Navy Medical Universtiy, PLA
Eligibility
Sex/Gender
Female
Age
18 Years to 45 Years
Inclusion criteria
Inclusion criteria: 1. hospitalized expectant mothers without serious complications, 2. patients who provided written informed consent to participate, and 3. patients with primary school or higher education.
Exclusion criteria
Exclusion criteria: 1. patients with serious pregnancy complications; 2. patients who were informed of the study but did not agree to participate, and 3. patients who were illiterate.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| satisfaction;rate of medical services received; | — |
Countries
China
Contacts
Public ContactXu Ping
Faculty of Health Service, Navy Medical University
Outcome results
None listed