Clinical Trials Directory

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UnknownNCT06237088

Mother-infant Connection Strategy Program

Mother-infant Connection Strategy Program: Impact on Psychological Distress and Mother-infant Bonding in Women

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
142 (estimated)
Sponsor
National Taipei University of Nursing and Health Sciences · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Accepted

Summary

This study evaluated the long-term effects of an online mindfulness-based program on the psychological distress and mother-infant bonding of women

Detailed description

The aim of this study was to test the efficacy of an online mindfulness program in reducing women's perceived stress, anxiety, depression, and in enhancing mindfulness and mother-infant bonding compared to a control group. The investigators hypothesize that the use of an online mindfulness program or an eight-week mindfulness program by the two experimental groups will lead to improved mood symptoms and mother-infant bonding compared with the control group. A randomized controlled trial comparing three groups of healthy, singleton pregnant women was conducted using the Random Allocation Software (Saghaei, 2004). We used G-Power 3.1.9 for Windows to analyze the minimum effect size that would be statistically significant with an 80% probability, using an alpha error probability of 0.05 in the "ANOVA: Repeated measures, between factors" option. We inputted 3 for the number of groups, 4 for the number of measurements, 0.5 for the correlation between repeated measures, and factored in a 20% attrition rate. There are 41 women in each group.

Conditions

Interventions

TypeNameDescription
OTHERonline mindfulness programThe intervention includes an eight-week internet-based mindfulness program. The program introduces participants to a new mindfulness topic every week. These topics are heavily inspired by the eight-week mindfulness programs.
OTHEReight-week mindfulness programsThe intervention consists of 2.5-hour classes per week over a period of eight weeks.

Timeline

Start date
2023-01-30
Primary completion
2025-01-30
Completion
2026-01-30
First posted
2024-02-01
Last updated
2024-02-01

Locations

1 site across 1 country: Taiwan

Source: ClinicalTrials.gov record NCT06237088. Inclusion in this directory is not an endorsement.