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A Cross-sectional, Observational Multicenter Study to Assess the Reasons for Choosing the 3-year Hormonal IUD and Level of IUDs Knowledge Among Women Aged 18 to 29 Years

A Cross-sectional, Observational Multicenter Study to Assess the Reasons for Choosing the 3-year Hormonal IUD and Level of IUDs Knowledge Among Women Aged 18 to 29 Years

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02903888
Acronym
ANALIA
Enrollment
886
Registered
2016-09-16
Start date
2016-09-08
Completion date
2017-12-23
Last updated
2018-01-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intrauterine Devices, Medicated

Brief summary

A cross-sectional, observational multicenter study to assess the reasons for choosing the 3-year hormonal IUD and level of IUDs knowledge among women aged 18 to 29 years. The study will be conducted in standard clinical practice conditions at public and private gynecology clinics and during a single study visit. Approximately 1,000 women aged 18 to 29 years who have freely chosen the 3 year hormonal IUD as their contraceptive method will be included in the study.

Interventions

Intrauterine delivery system Jaydess (13.5 mg levonorgestrel)

Sponsors

Bayer
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 29 Years
Healthy volunteers
No

Inclusion criteria

* Women aged 18 to 29 years. * Women who decided to initiate treatment with a 3-year hormonal IUD for contraception after being adequately counseled and informed of all contraceptive options by their physician during a routine clinical visit, prior to the study visit (insertion visit). * Women capable of reading and writing. * Women who signed informed consent.

Exclusion criteria

* Women currently participating in an interventional clinical trial. * Prescription of the 3-year hormonal IUD for non-contraceptive medical reasons.

Design outcomes

Primary

MeasureTime frameDescription
Reason for choosing Jaydess as intrauterine device (IUD)day 1The participants select the reason out of a given list of 15 possible reasons
Reason for switching to Jaydess if used another type of intrauterine device beforeday 1The participants select the reason out of a given list of 10 possible reasons
Knowledge of Jaydess or other IUDs prior to the visitday 1The participants select the reason out of a given list of 3 possible reasons
Is the first intrauterine device prescribed?day 1Possible reasons: Yes or No
Person who encouraged the use of jaydess?day 1The participants select the answer out of a given list of 5 possible people

Secondary

MeasureTime frameDescription
Marital statusday 1
Place of birthday 1
Place of residenceday 1
Educational levelday 1
Employmentday 1
Income levelday 1
Do you have children? (Y/N)day 1
Number of childrenday 1
Has she had some birth vaginally? (Y/N)day 1
Reason for not using Jaydess or other intrauterine delivery system (IUD) beforeday 1The participants select the reason out of a given list of 12 possible reasons
Do you plan to have (more) children? (Yes/No/Unknown)day 1
When she plans to have (more) childrenday 1
Frequency of menstrual bleedingday 1
Regularity of menstrual bleedingday 1
Quantity of menstrual bleedingday 1
Duration of menstrual bleedingday 1
Absence of menstrual bleedingday 1
Questionnaire concerning the physicians' characteristicsday 1The questionnaire consists of 7 questions
Date of last birthday 1
Uterine length as measured by ultrasonographyday 1
Presence of dysmenorrhea (Y/N)day 1
Current contraception methodday 1The participants select out of a given list of 20 options
Date of birthday 1

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026