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Clinical Trials/NCT04829877
NCT04829877
Recruiting
Not Applicable

Trajectory of Psychological Distress Among Infertility Women: Efficacy and Mechanism of Mind-body Intervention With Heart Rate Variability Biofeedback

Taipei Medical University1 site in 1 country750 target enrollmentApril 19, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Infertility
Sponsor
Taipei Medical University
Enrollment
750
Locations
1
Primary Endpoint
Anxiety
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

Background: Infertility is a serious reproductive health issue and affects 48.5 million couples worldwide. Women undergoing fertility treatment often experienced psychological distress but also social stigma that is close linked to later pregnancy outcome. Despite the advancement in assisted reproductive technology, effective interventions for reducing stress, anxiety, and depressive symptoms for infertility women remain lacking.

Objectives: The objective of this proposal is to evaluate the efficacy of web-based mind-body intervention combining HRV biofeedback on the infertility women's anxiety symptoms, levels of depression, HRV function, mindful awareness, infertility self-efficacy, and pregnancy rates.

Methods: We plan to conduct a randomized controlled trial on the web-based mind-body intervention combining heart rate variability biofeedback. Eligible women will be recruited and randomized into three groups. Intention-to-treat analysis and mixed regression modeling will be used to estimate the effectiveness of the interventions.

Anticipatory results: Effective strategies will be determined for infertility women.

Detailed Description

A designed data entry system for the current study will be developed to ensure an error-proof process. It is important to inspect data for outliers, wild code, and consistency to maintain the data quality in the pre-analysis data phase. We will assess the amount and pattern of missing values by using descriptive statistics, such as frequency and percentage. The pattern of missing data will be identified and decide whether the missing completely at random or not. The appropriate corresponding method will be adopted for the subsequent statistical analyses. For example, the mean imputation is considered when the percentage of items missing at a given questionnaire is less than 10 %. The mean imputation will be used to replaces a missing value with the item mean when applicable. The comparison between complete case analysis and imputation data will be performed to assess the reliability and validity of the results.

Registry
clinicaltrials.gov
Start Date
April 19, 2022
End Date
April 2025
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Shu Yu Kuo

Principal investigator

Taipei Medical University

Eligibility Criteria

Inclusion Criteria

  • 20-year-old and above
  • Seeking infertility care
  • Contemplating pregnancy
  • Intended to start their ART cycle
  • Able to speak Taiwanese or Mandarin

Exclusion Criteria

  • Diagnosis of cardiovascular disease, depressive disorder, anxiety disorder, cardiac arrhythmia
  • Already had started their ART treatment
  • Taking medications that might affect ANS activity

Outcomes

Primary Outcomes

Anxiety

Time Frame: 3 month post-intervention

Anxiety symptoms will be assessed using the Taiwanese version of the State Anxiety Inventory (SAI).

Secondary Outcomes

  • Infertility self-efficacy(Baseline, post-intervention 1 week, month 1 , 2 and 3)
  • Mindful awareness(Baseline, post-intervention 1 week, month 1 , 2 and 3)
  • HRV function(Baseline, post-intervention 1 week, month 1 , 2 and 3)
  • Depressive symptoms(Baseline, post-intervention 1 week, month 1 , 2 and 3)
  • Pregnancy rates(15 days after embryo transfer or ultrasound)

Study Sites (1)

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