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Prevalence of Female Circumcision Among Young Women in Beni-Suef, Egypt (FC)

18. december 2017 opdateret af: Nesreen Abdel Fattah Abdullah Shehata, Beni-Suef University

Prevalence of Female Circumcision Among Young Women in Beni-Suef, Egypt. A Cross-sectional Study

Female circumcision (FC) is a deeply-rooted practice in Egypt with deblitating physical and psychological consequences, however the previous two decades witnessed sincere efforts to counterfight this practice. The objective of this study is to investigate the prevalence of circumcision among young women (12-25 years) in Beni-Suef , Egypt.

Studieoversigt

Status

Afsluttet

Betingelser

Detaljeret beskrivelse

This cross-sectional study was conducted on a total of 3353young women residing urban and rural quraters in Beni-Suef City. Data was collected usinga questionnaire that included information about the socio-demographic charcteristics of the women, their gynecological data, exposure to FC, and complaints associated with menses during the previous year.

Undersøgelsestype

Observationel

Tilmelding (Faktiske)

3353

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

      • Cairo, Egypten, 018
        • Beni-Suef University

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

12 år til 25 år (Barn, Voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Kvinde

Prøveudtagningsmetode

Sandsynlighedsprøve

Studiebefolkning

The urban Metropolitan of Beni-Suef City was classified according to the socioeconomic level of its quarters to low, middle, and high levels. Out of each level, one quarter was selected randomly, by a card withdrawal, where households residing these quarters were chosen using a random start. For the rural villages surrounding the urban Metropolitan, three villages were selected randomly; one on the road to the North, one on the road to the West, and the last one on the road to the South. Each village was clustered roughly into two sites; one to the East of the water channel and one to the West of the same water channel.

In both urban and rural areas, a trained team of data collectors visited the selected households. Householders were informed briefly of the study and the residing women aged between 12 and 25 years were invited to participate and then interviewed.

Beskrivelse

Inclusion Criteria:

  • Young women aged 12 to 25 years living in Beni-Suef city of Egypt. the urban Metropolitan of Beni-Suef City was classified according to the socioeconomic level of its quarters to low, middle, and high levels. Out of each level, one quarter was selected randomly, by a card withdrawal, where households residing these quarters were chosen using a random start. For the rural villages surrounding the urban Metropolitan, three villages were selected randomly; one on the road to the North, one on the road to the West, and the last one on the road tothe South. Each village was clustered roughly into two sites; one to the East of the water channel and one to the West of the same water channel

Exclusion Criteria:

  • Women from other places in Egypt.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Gynecological manifestations measured by a questionnaire.
Tidsramme: one year
A questionnaire included questions about the manifestations associated with menses and average duration of dysmenorrhea during the previous year.
one year

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
social status measured by a questionnaire
Tidsramme: one year
A questionnaire included questions about age at menarche, social, educational and work status.
one year

Andre resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
working status measured by a questionnaire
Tidsramme: One year
For data collection, a questionnaireof two sections was prepared;the first section included socio-demographic data, social status, working status and educational level,age at menarche, menstrual cycle duration and flow days, in addition to exposure to circumcision. The second section includedquestions about the manifestations associated with menses and average duration of dysmenorrhea
One year

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Publikationer og nyttige links

Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.

Generelle publikationer

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

3. april 2017

Primær færdiggørelse (Faktiske)

15. juli 2017

Studieafslutning (Faktiske)

15. juli 2017

Datoer for studieregistrering

Først indsendt

8. december 2017

Først indsendt, der opfyldte QC-kriterier

18. december 2017

Først opslået (Faktiske)

22. december 2017

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

22. december 2017

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

18. december 2017

Sidst verificeret

1. december 2017

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • Beni-Suef 14

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

INGEN

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

Studerer et amerikansk FDA-reguleret lægemiddelprodukt

Ingen

Studerer et amerikansk FDA-reguleret enhedsprodukt

Ingen

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

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