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Trajectory of Psychological Distress Among Infertility Women

Primary Purpose

Infertility, Heart Rate Variability, Biofeedback

Status
Recruiting
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
Web-based mind-body intervention with HRVB
Web-based mind-body intervention
Sponsored by
Taipei Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Infertility focused on measuring infertility, mind-body intervention, heart rate variability, biofeedback, psychological distress

Eligibility Criteria

20 Years - 60 Years (Adult)FemaleAccepts Healthy Volunteers

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

Sites / Locations

  • Infertility clinicRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

No Intervention

Arm Label

Web-based mind-body intervention with HRVB

Web-based mind-body intervention

Control

Arm Description

Both standard usual care and the web-based mind-body intervention with HRV biofeedback (MBI-HRVB) will be provided to the participants. The web-based mind-body intervention with HRV biofeedback program consisted of 5-week training sessions and breathing training.

Both standard usual care and the web-based mind-body intervention will be provided to the participants. The web-based mind-body intervention program consisted of 5-week training sessions.

The women in the control group will receive the standard usual care provided at the fertility clinic. The standard care protocols encompass elements such as routine assessment and health education at each visit. Participants enrolled in the control group will be approached once a week by a nurse to provide health consultation about fertility treatment, medication, signs, and symptoms of discomfort for five weeks.

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

Depressive symptoms
The Taiwanese version of the Beck Depression Inventory (BDI) will be used to assess depressive symptoms among infertility women.
HRV function
The HRV signal will be measured using standard equipment.
Mindful awareness
The Taiwanese version of the Five Facet Mindfulness Questionnaire (FFMQ) will be adopted to assess levels of mindfulness.
Infertility self-efficacy
The infertility Self-Efficacy Scale (ISE) will be used for studied women.
Pregnancy rates
Clinical pregnancy will be defined as a positive blood, urinary pregnancy test.

Full Information

First Posted
March 31, 2021
Last Updated
April 12, 2023
Sponsor
Taipei Medical University
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1. Study Identification

Unique Protocol Identification Number
NCT04829877
Brief Title
Trajectory of Psychological Distress Among Infertility Women
Official Title
Trajectory of Psychological Distress Among Infertility Women: Efficacy and Mechanism of Mind-body Intervention With Heart Rate Variability Biofeedback
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
April 19, 2022 (Actual)
Primary Completion Date
January 2024 (Anticipated)
Study Completion Date
January 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Taipei Medical University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infertility, Heart Rate Variability, Biofeedback
Keywords
infertility, mind-body intervention, heart rate variability, biofeedback, psychological distress

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
750 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Web-based mind-body intervention with HRVB
Arm Type
Experimental
Arm Description
Both standard usual care and the web-based mind-body intervention with HRV biofeedback (MBI-HRVB) will be provided to the participants. The web-based mind-body intervention with HRV biofeedback program consisted of 5-week training sessions and breathing training.
Arm Title
Web-based mind-body intervention
Arm Type
Experimental
Arm Description
Both standard usual care and the web-based mind-body intervention will be provided to the participants. The web-based mind-body intervention program consisted of 5-week training sessions.
Arm Title
Control
Arm Type
No Intervention
Arm Description
The women in the control group will receive the standard usual care provided at the fertility clinic. The standard care protocols encompass elements such as routine assessment and health education at each visit. Participants enrolled in the control group will be approached once a week by a nurse to provide health consultation about fertility treatment, medication, signs, and symptoms of discomfort for five weeks.
Intervention Type
Behavioral
Intervention Name(s)
Web-based mind-body intervention with HRVB
Intervention Description
The web-based mind-body intervention with HRVB contains the following components: 1) Breathing training with HRV biofeedback; 2) 5 different topics will be included ; 3) Home exercise of slow breathing and mindfulness exercise.
Intervention Type
Behavioral
Intervention Name(s)
Web-based mind-body intervention
Intervention Description
The web-based mind-body intervention will receive 5 different topics courses.
Primary Outcome Measure Information:
Title
Anxiety
Description
Anxiety symptoms will be assessed using the Taiwanese version of the State Anxiety Inventory (SAI).
Time Frame
Baseline
Title
Anxiety
Description
Anxiety symptoms will be assessed using the Taiwanese version of the State Anxiety Inventory (SAI).
Time Frame
1 week post-intervention
Title
Anxiety
Description
Anxiety symptoms will be assessed using the Taiwanese version of the State Anxiety Inventory (SAI).
Time Frame
1 month post-intervention
Title
Anxiety
Description
Anxiety symptoms will be assessed using the Taiwanese version of the State Anxiety Inventory (SAI).
Time Frame
2 month post-intervention
Title
Anxiety
Description
Anxiety symptoms will be assessed using the Taiwanese version of the State Anxiety Inventory (SAI).
Time Frame
3 month post-intervention
Secondary Outcome Measure Information:
Title
Depressive symptoms
Description
The Taiwanese version of the Beck Depression Inventory (BDI) will be used to assess depressive symptoms among infertility women.
Time Frame
Baseline, post-intervention 1 week, month 1 , 2 and 3
Title
HRV function
Description
The HRV signal will be measured using standard equipment.
Time Frame
Baseline, post-intervention 1 week, month 1 , 2 and 3
Title
Mindful awareness
Description
The Taiwanese version of the Five Facet Mindfulness Questionnaire (FFMQ) will be adopted to assess levels of mindfulness.
Time Frame
Baseline, post-intervention 1 week, month 1 , 2 and 3
Title
Infertility self-efficacy
Description
The infertility Self-Efficacy Scale (ISE) will be used for studied women.
Time Frame
Baseline, post-intervention 1 week, month 1 , 2 and 3
Title
Pregnancy rates
Description
Clinical pregnancy will be defined as a positive blood, urinary pregnancy test.
Time Frame
15 days after embryo transfer or ultrasound

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Shu-Yu Kuo, Phd
Phone
+886-2-2736-1661
Ext
6301
Email
sykuo@tmu.edu.tw
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shu-Yu Kuo, Phd
Organizational Affiliation
Taipei Medical University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Infertility clinic
City
Taipei
ZIP/Postal Code
110
Country
Taiwan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jin-Ru Chang, BS

12. IPD Sharing Statement

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Trajectory of Psychological Distress Among Infertility Women

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