Recruitment

Recruitment Status
Not yet recruiting
Estimated Enrollment
Same as current

Summary

Conditions
Pregnant Women
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: Double (Investigator, Outcomes Assessor)Primary Purpose: Health Services Research

Participation Requirements

Age
Between 18 years and 125 years
Gender
Only males

Description

Intervention Building a health education team, developing protocols and training staff Two obstetric care specialists, eight registered nursing supervisors and two masters-level research nurses comprised a health education team for this study. Obstetric care specialists will be primarily responsible...

Intervention Building a health education team, developing protocols and training staff Two obstetric care specialists, eight registered nursing supervisors and two masters-level research nurses comprised a health education team for this study. Obstetric care specialists will be primarily responsible for guiding and monitoring the execution of the intervention. Registered supervisor nurses will organize education sessions for participating women and communicated with women in education sessions. Research nurses will lead the work of designing the study, collected data and conducted analysis, but in order to avoid critical biases in data analysis and interpretation, they do not participate in any education sessions designed in the intervention protocols. Two research nurses approach pregnant women on the day when they are just admitted to hospital for delivery with pregnancies that are considered full term (pregnancy week is between 37+0 and 41+6) but with no sign of labor or getting into the first stage of labor (Women can prefer to stay in hospital as their pregnancies turn full, and wait for delivery). The research nurses ask women to complete a questionnaire designed with perinatal maternal health literacy scale for baseline MHL assessment. Eligible pregnant women will be informed about the aims, contents, and procedures of the study. Participation will be based on voluntary, and informed consent was signed by each participating woman. Before commencing the trial, a one-day team workshop will be organized Building a health education team, developing protocols and training staff Two obstetric care specialists, eight registered nursing supervisors and two masters-level research nurses comprise a health education team for this study. Obstetric care specialists will be primarily responsible for guiding and monitoring the execution of the intervention. Registered supervisor nurses organize education sessions for participating women and communicated with women in education sessions. Research nurses lead the work of designing the study, collected data and conducted analysis, but in order to avoid critical biases in data analysis and interpretation, they do not participate in any education sessions designed in the intervention protocols. Before commencing the trial, a one-day team workshop will organized.

Tracking Information

NCT #
NCT04858945
Collaborators
Aalto University
Investigators
Study Chair: Guizhi Cheng Anhui Provincial Hospital