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NCT04556630 Clinical Trial

Experience of Lock Down Related to the Covid-19 Epidemic and Its Impact on the Project of Parenthood

Assisted Reproduction Clinical Trial

— CONFIN-AMP  

Official title:
Evaluation of the Experience of Lock Down Related to the Covid-19 Epidemic and Its Impact on the Project of Parenthood of the Couples Followed in Assisted Reproduction

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04556630
Other study ID # 2020_65
Secondary ID 2020-A01810-39
Status Completed
Phase
First received
Last updated
Start date December 9, 2020
Est. completion date June 22, 2021

Study information
Verified date February 2022
Source University Hospital, Lille
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Observational, descriptive, cross-sectional, monocentric study, This Study is proposed to all couples followed in Assisted Reproduction and CECOS Nord for whom the protocols were stopped when they entered into confinement related to the Covid-19 epidemic on 13 March 2020.

Recruitment information / eligibility
Status Completed
Enrollment 400
Est. completion date June 22, 2021
Est. primary completion date June 22, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - couples followed up in Assisted Reproduction and CECOS Nord - the cessation of assistance reproduction protocols related to the Covid-19 outbreak on March 13, 2020. - acceptance of teleconsultation Exclusion Criteria: - Individuals refusing to participate in the study during the teleconsultation with the referring practitioner. I- ndividuals who do not respond to the questionnaire

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
France Hop Calmette Chu Lille Lille

Sponsors (1)
Lead Sponsor Collaborator
University Hospital, Lille

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Level of anxiety and/or depression of MPA patients (male and female couples) by Hospital Anxiety and Depression Scale (HAD) score. Baseline
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