NCT04426942

Brief Summary

We wish to evaluate sexuality during pregnancy between spontaneous pregnancies and resulting from assisted procreation The literature is poor on thie subject

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
350

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jun 2020

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

June 5, 2020

Completed
6 days until next milestone

First Posted

Study publicly available on registry

June 11, 2020

Completed
9 days until next milestone

Study Start

First participant enrolled

June 20, 2020

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2020

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2020

Completed
Last Updated

June 11, 2020

Status Verified

June 1, 2020

Enrollment Period

2 months

First QC Date

June 5, 2020

Last Update Submit

June 8, 2020

Conditions

Pregnancy RelatedAssisted Reproduction

Keywords

assisted reproduction

Outcome Measures

Primary Outcomes (1)

  • Evaluation of sexual functioning with Female Sexual Function Index (FSFI) test

    In the second trimester of the pregnancy

Study Arms (2)

Spontaneous pregnancy

Other: survey

Assisted reproduction pregnancy

Other: survey

Interventions

surveyOTHER

survey on sexuality during pregnancy

Assisted reproduction pregnancySpontaneous pregnancy

Eligibility Criteria

Age18 Years+
Sexfemale(Gender-based eligibility)
Gender Eligibility DetailsPregnant women
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Pregnant women

You may qualify if:

  • physiological pregnancy
  • pregnancy from assisted reproduction
  • age over 18
  • to understand french
  • patient's agreement

You may not qualify if:

  • pathological pregnancy

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Matthieu Dap

Nancy, 54000, France

RECRUITING

MeSH Terms

Interventions

Surveys and Questionnaires

Intervention Hierarchy (Ancestors)

Data CollectionEpidemiologic MethodsInvestigative TechniquesHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public Health

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Docteur

Study Record Dates

First Submitted

June 5, 2020

First Posted

June 11, 2020

Study Start

June 20, 2020

Primary Completion

September 1, 2020

Study Completion

December 1, 2020

Last Updated

June 11, 2020

Record last verified: 2020-06

Locations

FR(1)