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Factors Associated With the Absence of Contraception at Women Seeking a Voluntary Termination of Pregnancy

31 januari 2022 uppdaterad av: Centre Hospitalier Intercommunal Creteil

Factors Associated With the Absence of Contraception at the Time of Unplaned Pregnancy Among Women Seeking a Voluntary Termination of Pregnancy

The study will be offered to all women who are consultant for an abortion plan are seen in consultation at the orthogeny center where the study will be conducted. Of these 700 women, about 10% will not agree to participate in the study and 10% will not meet the inclusion criteria. Thus it's plane to include 560 patients in the study.

Studieöversikt

Status

Upphängd

Betingelser

Detaljerad beskrivning

In 1967, the Neuwirth law allowed women to control their fertility by establishing the right to contraception as a principle. Since then, they have continued to take ownership of the various contraceptive methods, which are regularly renewed.

Contraceptive coverage is important in France as it is estimated that 92% of women of childbearing age use a contraceptive method. The pill remains the most widely used method of contraception (36.5%), ahead of the intrauterine device (25.6%) condoms (15.5%) Several laws have been introduced from 1967 to today to facilitate access to sexual health care: screening for sexually transmitted infections, free provision of emergency contraception to minors, non-prescription delivery of emergency contraception, free consultation at a family planning and education center, voluntary termination of pregnancy 100%, reimbursement of condoms by social security.

Despite all the measures put in place, it is now clear that the number of unplanted pregnancies is decreasing slightly and the number of abortion has remained stable since 2001.

According to the latest literature data, several socio-demographic factors appear to play a role in the rate of use of voluntary termination of pregnancy., including age, socio-cultural level, marital and economic status and ethnic origin. All the more striking, it appears that while voluntary termination of pregnancy are mainly related to contraceptive failures, one third of them involve women who do not have contraception. According to the latest Ined survey, and in accordance with other data from the literature, the factors associated with the absence of contraceptive use are multiple: ignorance about fertility, family or cultural context, cost of contraceptive methods or lack of information related to them.

While these studies have looked at the reasons given by women for the lack of contraception, with little data on the characteristics of these women, particularly socio-demographics and their reproductive history and in particular in the context of unwanted pregnancy. This finding leads us to question the factors associated with the absence of contraception among women in demand of a voluntary termination of pregnancy.

Studietyp

Observationell

Inskrivning (Förväntat)

560

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

      • Villeneuve-Saint-Georges, Frankrike
        • CHI Villeneuve St Georges

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

18 år och äldre (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Kvinna

Testmetod

Icke-sannolikhetsprov

Studera befolkning

Protocol proposed to woman who wanted a voluntary termination of pregnancy

Beskrivning

Inclusion Criteria:

  • woman of 18 years of age or older;
  • Being French-speaking;
  • request for a medical or instrumental voluntary termination of pregnancy
  • No opposition to participation in the protocol
  • Be affiliated with a social security plan

Exclusion Criteria:

  • desired pregnancy

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Association between absence of contraception and socio-demographic factors, characteristics of pregnancy abortion and medical follow-up
Tidsram: 1 hour
Statistically significant association between the absence of contraception in patients consulting for a voluntary termination of pregnancy and socio-demographic factors, characteristics of voluntary termination of pregnancy abortion and characteristics related to medical follow-up
1 hour

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Prescription and dispensing of contraception
Tidsram: 1 hour
Prevalence of patients informed about the prescription and dispensing of contraception including emergency contraception
1 hour
Existence of family planning centers
Tidsram: 1 hour
Prevalence of patients informed about the existence of family planning centers
1 hour
Emergency contraception
Tidsram: 1 hour
Prevalence of women who have used emergency contraception
1 hour
Price and reimbursement of condoms
Tidsram: 1 hour
Prevalence of women informed about the price and reimbursement of condoms
1 hour
Knowledge of conception
Tidsram: 1 hour
Estimate the percentage of women who thought they could get pregnant at the time of the intercourse that led to this pregnancy
1 hour
Fertile window
Tidsram: 1 hour
Prevalence of women who use a method to track their fertile window
1 hour
Affection of fertility
Tidsram: 1 hour
Estimate the percentage of women who think that contraception can affect their fertility
1 hour

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Förväntat)

1 november 2022

Primärt slutförande (Förväntat)

1 november 2022

Avslutad studie (Förväntat)

1 november 2022

Studieregistreringsdatum

Först inskickad

11 februari 2021

Först inskickad som uppfyllde QC-kriterierna

31 mars 2021

Första postat (Faktisk)

2 april 2021

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

1 februari 2022

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

31 januari 2022

Senast verifierad

1 januari 2022

Mer information

Termer relaterade till denna studie

Andra studie-ID-nummer

  • NOCONTRAIVG
  • 2021-A00298-33 (Annan identifierare: ID-RCB)

Läkemedels- och apparatinformation, studiedokument

Studerar en amerikansk FDA-reglerad läkemedelsprodukt

Nej

Studerar en amerikansk FDA-reglerad produktprodukt

Nej

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