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Clinical Trials/NCT04396210
NCT04396210
Completed
Not Applicable

Patients Perspectives on Discontinuation of Their Fertility Treatment Due to the COVID-19 Pandemic

University Hospital, Ghent1 site in 1 country389 target enrollmentStarted: May 14, 2020Last updated:

Overview

Phase
Not Applicable
Status
Completed
Enrollment
389
Locations
1
Primary Endpoint
Patients perspectives on the abruptly discontinuation of their fertility treatment by using a questionnaire

Overview

Brief Summary

The COVID-19 pandemic brought new challenges to our nationwide healthcare system, with rapid escalation of the number of affected individuals over a handful of weeks. From March 13, a first set of measures was taken to minimise the spread of the virus, which largely impacted societal and economical daily life. A view days later, on March 17, the country was put in "lockdown" and all non-urgent medical treatments were cancelled or postponed. As recommended by the major scientific fertility societies, all non-ivf fertility treatments were discontinued abruptly, whereas started ivf stimulations were continued until oocyte aspiration, where after a freeze-all strategy was applied.

There is little information available for women aiming for pregnancy or embarking on assisted conception. Given the modelling of the pandemic, including the time to peak and subsequent tail, considerable delays in conception to substantially attenuate risk may be required, which will inevitably impact patients wellbeing and overall success rates.

A questionnaire was developed to explore patients perspectives on different aspects of their fertility treatment during the COVID-19 pandemic.

The questionnaire contains the following sections:

  • demographic variables;
  • questions regarding the fertility history of the respondent;
  • questions regarding the impact of fertility treatment cancellation / postponing fertility treatment during COVID-19 on their life, psychological wellbeing and relationship;
  • questions regarding continuing medical treatment on their own, or seeking treatment elsewhere;
  • questions regarding the satisfaction of measures taken by their fertility center regarding the COVID-19 pandemic;
  • questions regarding expectations of further treatments, with focus on safety issues related to the COVID-19 pandemic.

Eligible patients will be selected electronically from our database and digital agenda. After selection, patients will be contacted via email to participate. Two reminders will be send in case the questionnaire is not filled out: a first reminder after one week, a second reminder after two weeks.

Study Design

Study Type
Observational
Observational Model
Other
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 47 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • patients that did not start a fertility treatment yet ("intake group") OR;
  • patients for which a treatment plan was made, but treatment was postponed ("before treatment") OR;
  • patients who were undergoing a non-inf treatment cycle (ovulation-induction (OI), intra-uterine insemination (IUI)) and whose cycle was cancelled after starting the treatment cycle ("non-ivf treatment group") OR;
  • patients who were undergoing a cryo cycle and whose cycle was cancelled after starting the treatment cycle ("cryo treatment group") OR;
  • patients who were undergoing an IVF treatment cycle and for whom fresh embryo transfer was cancelled (freeze-all group).

Exclusion Criteria

  • Language other than Dutch

Outcomes

Primary Outcomes

Patients perspectives on the abruptly discontinuation of their fertility treatment by using a questionnaire

Time Frame: During the COVID-19 pandemic, from March 2020 till June 2020

Patients reproductive behaviour by using a questionnaire

Time Frame: During the COVID-19 pandemic, from March 2020 till June 2020

Patients views on resuming fertility treatment by using a questionnaire

Time Frame: During the COVID-19 pandemic, from March 2020 till June 2020

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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