Mindfulness-based Prenatal Education on Women

  • STATUS
    Recruiting
  • days left to enroll
    69
  • participants needed
    76
  • sponsor
    National Taipei University of Nursing and Health Sciences
Updated on 27 March 2021

Summary

The purpose of this study is to explore the differences between stress, anxiety, depression, mindfulness, salivary amylase activity and postnatal maternal outcomes for prenatal mental disorders women with mindfulness prenatal education program

Description

The aim of this study was to test the efficacy of a Mindfulness prenatal education program in reducing pregnant women's perceived stress, anxiety, depression, mindfulness, salivary alpha-amylase compared to a control group. The investigators hypothesize that use of the mindfulness prenatal education program by study group will lead to improved related mood symptoms compared with control group.

Randomized Controlled Trial comparing two education programs with health and singleton pregnant women is run by the Random Allocation Software (Saghaei, 2004). Use the G-Power 3.1.9 windows: repeated measures and between factors among two groups to calculate the number of samples, and setting the power = .8, = .05, effect size = .25. The estimated number of samples may be lost 20%, total 76 samples.

Details
Condition anxiety/depression
Treatment Mindfulness-based prenatal education, Application for prenatal education, Hospital-based antenatal education
Clinical Study IdentifierNCT04693130
SponsorNational Taipei University of Nursing and Health Sciences
Last Modified on27 March 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Subjects were at the age over 20
Could speak and read Chinese fluently
Willing and be ale to attend the education program

Exclusion Criteria

Taking medication for diagnosing mental illness
With complicated or high-risk pregnancies
Clear my responses

How to participate?

Step 1 Connect with a study center
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  • You can expect the study team to contact you via email or phone in the next few days.
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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