DIU-QoL. Quality of Life Evaluation in Intrauterine Device Users.

Bayer207 enrolled

Overview

Knowledge about the impact on quality of life of women initiating IUD in the Spanish population at baseline and after 12 months of use.

Study Type

OBSERVATIONAL

Enrollment

207

Conditions

Contraception

Interventions

Levonorgestrel IUD or Copper IUDDRUG

Women who initiate the use of an IUD at the time of the study.

Eligibility

Sex: FEMALEMin age: 18 YearsMax age: 49 Years

Medical Language ↔ Plain English

Inclusion Criteria: * 18-49 years old female. * Women who is visited by a gynecology or primary care physician and starts contraception with an IUD/IUS. * Women that has not used hormonal contraception in any form in the last 3 months. * Women who have no problems listening, reading or writing. * Women who gives their written consent to participate in the study. Exclusion Criteria: * Women who have contraindications to use IUDs. * Women with previous experience with IUDs. * Women who initiates the use of IUDs for other purposes other than contraception. * Woman who is participating in a clinical trial at the time of initiating the study.

Locations (1)

Unnamed facility

Many Locations, Spain

Outcomes

Primary Outcomes

Impact on quality of life of women initiating IUD in a Spanish population assessed by questionnaire.

Time frame: After 12 months

Secondary Outcomes

Demographic Data (Age, Place of Birth, Level of Education, Employment status, Personal marital situation, etc.) assessed by questionnaire.

Time frame: Baseline

Data from ClinicalTrials.gov

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