Effects of the couple-based mobile program delivered at each stage of the procedure to improve the quality of life of infertile couples undergoing intrauterine inseminatio
Not Applicable
Completed
- Conditions
- InfertilityUrological and Genital Diseases
- Registration Number
- ISRCTN87611792
- Lead Sponsor
- Seoul Medical Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Women and their husbands (couples) who were having IUI were eligible to participate. The inclusion criteria were:
1. Couples who understood the purpose of the study and gave written consent to participate in the study
2. Couples diagnosed with infertility and undergoing IUI
3. Couples without health problems other than infertility, such as mental illness
4. A couple who can use the Internet through a mobile device
Exclusion Criteria
1. Couples in which at least one of the couples is taking medications such as anti-anxiety drugs or tranquilizers
2. Cases in which at least one of the couples does not use a mobile device, those who did not agree to participate voluntarily
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method General and infertility-related characteristics (10 questions) and the study variables (infertility stress, anxiety, infertility self-efficacy, marital relationship, social support, and infertility quality of life) measured using a pre-survey on the first day of the IUI process
- Secondary Outcome Measures
Name Time Method Infertility stress, anxiety, infertility self-efficacy, couple relationship, social support, and infertility quality of life, measured using a second survey after completing all interventions