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Fysioterapi og Rehabiliteringsstuderendes Inkontinens Vidensniveau

1. oktober 2026 opdateret af: Asli Demirtaş, Nigde Omer Halisdemir University

Udredning af fysioterapi og rehabiliteringsstuderendes inkontinensvidensniveau og holdninger til behandling

The aim of the study is to examine the urinary incontinence knowledge level and attitudes towards treatment in Physiotherapy and Rehabilitation students. With this study, students' knowledge levels about urinary incontinence and treatment parameters will be determined, and it will be possible to show whether there is a difference between genders in terms of knowledge levels.

Studieoversigt

Status

Afsluttet

Detaljeret beskrivelse

The aim of the study is to examine the urinary incontinence knowledge level and attitudes towards treatment in Physiotherapy and Rehabilitation students. With this study, students' knowledge levels about urinary incontinence and treatment parameters will be determined, and it will be possible to show whether there is a difference between genders in terms of knowledge levels.

At least 260 students studying in the Physiotherapy and Rehabilitation Department in Turkey will be included in the study.

Undersøgelsestype

Observationel

Tilmelding (Faktiske)

437

Kontakter og lokationer

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

Studiesteder

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

18 år til 65 år (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ja

Køn, der er berettiget til at studere

Alle

Prøveudtagningsmetode

Ikke-sandsynlighedsprøve

Studiebefolkning

Physiotherapy and rehabilitation students in Turkey.

Beskrivelse

Inclusion Criteria:

  • Being a student of Physiotherapy and Rehabilitation department in Turkey
  • Being volunteer

Exclusion Criteria:

- Failing to complete surveys

Studieplan

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

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Observationsmodeller: COHORT
  • Tidsperspektiver: PROSPECTIVE

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
General information form
Tidsramme: Baseline

Demographic information such as age, gender, height, weight, university will be added to the general information form. In addition, in order to evaluate the level of knowledge of students on urinary incontinence, whether they took courses at the university, whether they followed a patient with urinary incontinence in their internships, the sources they have information about, whether they want to work in this field after graduation, which incontinence assessment methods they know and which treatment methods according to incontinence types, their preferences will be questioned.

Baseline
Incontinence Quiz
Tidsramme: Baseline

In order to determine the level of incontinence knowledge, Branch et al. It was developed by. The Turkish version study was conducted by Kara et al. made by. The 14-item test is answered as "I agree", "I don't agree" or "I don't know". The correct answer to statements 1, 4, 6, 8, 10, and 11 is "I agree". The correct answer for the remaining statements is "I do not agree". The answer 'I don't know' is calculated incorrectly. The total score ranges from 0 to 14, and a higher score indicates a higher level of knowledge and a more positive attitude towards Urinary Incontinence.

Baseline
Pelvic Floor Health Knowledge Quiz
Tidsramme: Baseline

The pelvic floor health knowledge quiz investigates the level of pelvic floor health knowledge in the Turkish population and was developed by Al'Deges and Çelenay in 2019. This test consists of 29 questions in three sub-dimensions related to pelvic floor function/dysfunction (8 items), risk and etiology (13 items), diagnosis and treatment (8 items). There is an option of 'Yes' for the positive items used in the test, 'no' for the negative items, and 'I don't know' for the participants who do not have any positive or negative opinion.

Baseline
Prolapse and Incontinence Knowledge Questionnaire
Tidsramme: Baseline

Prolapse and incontinence information questionnaire Shah et al. It was developed by in 2008 to evaluate incontinence and prolapse knowledge level. Turkish validity and reliability study by Çelenay et al. made by A questionnaire consisting of two 12-item scales; It consists of a urinary incontinence scale to assess women's knowledge of urinary incontinence and a POP scale to assess their knowledge of pelvic organ prolapse. 1 point is awarded for each correct answer and 0 points for each incorrect answer. A score of 0 is given as the answer "I don't know" means lack of knowledge about the current question. Total urinary incontinence and POP scale scores are calculated by summing up the number of correct answers. The total score for each scale can be 0 at the lowest and 12 at the highest.

Baseline

Samarbejdspartnere og efterforskere

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

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)

6. oktober 2022

Primær færdiggørelse (Faktiske)

6. juni 2023

Studieafslutning (Faktiske)

1. januar 2025

Datoer for studieregistrering

Først indsendt

18. januar 2023

Først indsendt, der opfyldte QC-kriterier

26. januar 2023

Først opslået (Faktiske)

27. januar 2023

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

6. oktober 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

1. oktober 2026

Sidst verificeret

1. oktober 2026

Mere information

Begreber relateret til denne undersøgelse

Yderligere relevante MeSH-vilkår

Andre undersøgelses-id-numre

  • 2022-1090

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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