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An Observational Study to Assess Quality of Life and Satisfaction of Young Women (Aged 18-29) Following 6 (±1) Months Using Jaydess as Their Contraceptive Method

A Cross-sectional, Observational Study to Assess Quality of Life and Satisfaction of Young Women (Aged 18-29) Following 6 (±1) Months Using Jaydess® as Their Contraceptive Method - The JULIA Study.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02574715
Acronym
JULIA
Enrollment
1039
Registered
2015-10-14
Start date
2015-09-18
Completion date
2016-09-28
Last updated
2017-06-29

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

Conditions

Quality of Life

Brief summary

This is a cross-sectional, multicenter observational study to assess quality of life in young Spanish women (aged 18 to 29) who use Jaydess® as their contraceptive method. The study will be conducted in standard clinical practice conditions at the private gynecology clinics and during a single study visit. Approximately 1,200 women who have been using the intrauterine delivery system (IUS) Jaydess® as their contraceptive method of choice for 6 (±1) months will be included in the study.

Interventions

DRUGLevonorgestrel (Jaydess, BAY86-5028)

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 have been using Jaydess as their contraceptive method for 6 (±1) months. * Women who have no comprehension, reading or writing challenges. * Women who have given informed consent in writing.

Exclusion criteria

* Contraindication to the use of Jaydess. * Prescription of Jaydess® for non-contraceptive medical reasons. * Women who are considered to be unsuitable to take part in the study by the investigator (e.g., poor understanding of the study characteristics, uncooperative, etc.). * Women who are currently taking part in any clinical trial.

Design outcomes

Primary

MeasureTime frameDescription
Quality of life as determined using the SEC-QoL scaleAt the single visitSEC-QoL (Spanish Contraception Society Quality of Life Questionnaire) is to assess the impact of contraceptive methods on health-related quality of life in women.

Secondary

MeasureTime frameDescription
Marital StatusAt the single visit
Place of BirthAt the single visit
Place of residence (province, town, city or rural area)At the single visit
Educational level (primary, secondary or higher education)At the single visit
Employment (working outside the home, working from home, unemployed, student)At the single visit
Maternity status (has children or plans to have children)At the single visit
Frequency attending this physician's clinic for family planning purposesAt the single visit
History of type of contraceptive useAt the single visit
Age (years)At the single visit
Prescription of Jaydess (date)At the single visit
Benefits perceived on ease and comfort of use by means of a structured interview (Yes, No)At the single visitThis will be assessed by a structured interview during which the subject will be asked a number of questions by her gynecologist with answers (Yes or No): Indicate the advantages of Jaydess (select all that apply): comfort, avoid forgetfulness, reversibility, long duration, contraception cost, ease of use, safety, reduction in the duration and amount of bleeding, regulation of menstrual cycle, decreased menstrual pain, immediate contraceptive activity, high efficacy.
Global assessment of the insertion by means of a structured interview for pain questions (any, slight, moderate, severe)At the single visit
Global assessment of the insertion by means of a structured interview for times questionsAt the single visit
Global assessment of the insertion (acceptable without discomfort, with a few of minimal discomfort or with an enormous discomfort and unacceptable)At the single visit
Global satisfaction with Jaydess, using a structured questionaireAt the single visitSatisfaction with Jaydess will be assessed using a structured questionnaire. The ease of use and impact on activities of daily living dimensions will be assessed on 3 items (ease and comfort of use, impact on activities of daily living and sexuality) for each dimension, each one with a 5-item Likert-like scale (where 1 = extremely unsatisfied and 5 = extremely satisfied).
Bleeding pattern features, using a questionnaire to compare current bleeding versus bleeding before the insertion of Jaydess as recalledAt the single visit
History of duration of contraceptive useAt the single visit

Countries

Spain

Outcome results

None listed

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