Infertility, Female Clinical Trial
— EMOT-IVFOfficial title:
What is the Impact of an E-tool Based Mindfulness Intervention on Psychological Outcomes Compared to no Intervention in Infertile Women Undergoing Assisted Reproductive Technique Treatments: A Randomized Controlled Study?
Verified date | June 2020 |
Source | University Hospital, Geneva |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Infertility and its treatments can have a significant impact on women's psychological health. Anxiety has a negative impact on quality of life during treatment and can lead to withdrawal of care. the investigators would like to test the effectiveness of an application available via the Internet that offers daily exercises such as mindfulness meditation. Women in the "treatment" group will be instructed to practice meditation exercises using the 15-minute daily application during in vitro fertilization treatment until pregnancy testing. Women in the control group will have the standard care of the centre. The investigators will measure the effectiveness of the intervention on anxiety, depression, quality of life and mindfulness aspects. The investigators will also assess the impact on the chances of pregnancy and stress.
Status | Not yet recruiting |
Enrollment | 150 |
Est. completion date | June 10, 2022 |
Est. primary completion date | June 10, 2020 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years to 42 Years |
Eligibility |
Inclusion Criteria: Participants fulfilling all of the following inclusion criteria are eligible for the study: - French-speaking - Women between the ages of 18-42 years - Scheduled for the first IVF treatment in HUG/CHUV/CPMA Lausanne - Access to a computer/smartphone/tablet with access to internet and a valid Email address - Informed Consent as documented by her signature on the form (Appendix Informed Consent Form) Exclusion Criteria: - Psychotropic medication - Ongoing psychiatric/psychological treatment - Known severe psychiatric co-morbidity |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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University Hospital, Geneva |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Anxiety state | The primary aim of the study is to evaluate the effect of an e-tool based intervention versus standard care without intervention on anxiety state measured by the French version of state trait anxiety index in infertile women undergoing ART. State trait anxiety index state scores will be evaluated by completion of a questionnaire at 3 time points: baseline, at the time of the oocyte retrieval, on the day before the pregnancy test (before the results). A score between 31 and 36 is considered as normal score. |
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