Contraception Pregnancy and Childbirth
Conditions
Interventions
This study will include an intervention group and a control group and data will be collected during a year in 6 autonomous regions in Spain. The health professionals participating in each unit will be
Sponsors
Universitat Rovira i Vigili
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Current participant inclusion criteria as of 28/05/2019: 1. Women aged 16 or older 2. Women aged 49 years or younger 3. Have primary studies and are proficient in Spanish and/or Catalan 4. Have access to the internet 5. Agree to voluntarily participate in the study Previous participant inclusion criteria: 1. Women aged 18 or older 2. Women aged 49 years or younger 3. Have primary studies and are proficient in Spanish and/or Catalan 4. Have access to the internet 5. Agree to voluntarily participate in the study
Exclusion criteria
Exclusion criteria: 1. Women aged 17 years or younger 2. Women aged 50 or older 3. Women who wish to have children before one year from the date of the consultation 4. Don't have access to internet 5. Don't understand Catalan and/or Spanish
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Adherence to treatment: compliance with dosage and method of administration and persistence in the duration of prescribed treatment, evaluated through a structured interview ad-hoc including questions about a) the compliance with the contraceptive method chosen in the clinical consultation, b) information about the usage of this method and c) unwanted pregnancy incidences. Assessed by a phone call at 1 month, 6 months and 1 year. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Sociodemographic characteristics of the patient: age, educational level, occupation, marital status/couple, assessed at a structured interview ad-hoc at the first contact in the clinical consultation 2. Medical history: smoking habits, HBP, uterine malformations, diabetes, assessed at a structured interview ad-hoc at the first contact in the clinical consultation 3. Obstetric and gynecological antecedents: menstrual formula, menarche, term or premature pregnancies, ectopic pregnancies, spontaneous abortions, IVE, gynecological reviews according to the guidelines of each community, active sexually transmitted diseases, living children, desire to have children, assessed at a structured interview ad-hoc at the first contact in the clinical consultation 4. Contraceptive method: contraceptive method contemplated by the patient before counseling, prejudices against other contraceptives, experiences with other methods, possible beneficial non-contraceptive effects, importance of the cost in her choice, women's behavior with respect to compliance (Morisky-Green's adherence to treatment), finally chosen contraceptive, incidents with the chosen method, management of the incidences, decisional conflict of the woman before the choice of the contraceptive method (O'Connor Scale), assessed at a structured interview ad-hoc at the first contact in the clinical consultation 5. Professional: satisfaction of the advisor or clinician with the use of the Digital HATD (Likert scale), acquired knowledge (ad-hoc knowledge test) assessed after the first year recruiting women for the study | — |
Countries
Spain
Outcome results
None listed