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Patient Education After Total Hip Arthoplasty

21. maj 2026 opdateret af: Sinem Yenil, PT, PhD, Pamukkale University

The Effect of Patient Education on Function, Quality of Life, and Activities of Daily Living After Total Hip Arthroplasty

Postoperative education is crucial for improving physical function, daily activity participation, and quality of life after total hip arthroplasty (THA). The aim of our study was to examine the effects of patient education on function, quality of life, and activities of daily living after THA. Patients who underwent primary THA were randomized into three groups: online education, brochure, and control. Pain (VAS), function (WOMAC), quality of life (WHOQOL-BREF), and daily living activities (IADL) were evaluated online before education and four weeks after discharge.

Studieoversigt

Status

Afsluttet

Betingelser

Intervention / Behandling

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

39

Fase

  • Ikke anvendelig

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

  • Voksen
  • Ældre voksen

Tager imod sunde frivillige

Ingen

Beskrivelse

Inclusion Criteria:

  • Participants aged 30 years or older
  • Who were undergoing primary THA surgery,
  • Able to understand and speak Turkish
  • Had access to and could use the internet and a smartphone.

Exclusion Criteria:

  • Who were undergoing revision THA surgery
  • Had previous major surgery on the operated limb,
  • Had comorbidities such as rheumatoid arthritis or cancer, motor disorders affecting ADL performance
  • Diagnosed psychiatric disorder, uncorrected hearing or vision impairment
  • Inability to participate in the online education program

Studieplan

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

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Enkelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Ingen indgriben: Styring
Aktiv komparator: Brochure
Andet: Brochure
Brochure group received an informational brochure with the same content.
Eksperimentel: Online education
Andet: Online Education
Online education group received an online education session prepared by the researchers, covering dislocation precautions, potential complications, and home exercise programs.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
The Turkish version of the Western Ontario McMaster University Osteoarthritis Index
Tidsramme: postoperative first day, postoperative 4th week
The Turkish version of the Western Ontario McMaster University Osteoarthritis Index (WOMAC), was used. The index includes 24 items divided into three subscales: pain (5 items, maximum score 20), stiffness (2 items, maximum score 8), and physical function (17 items, maximum score 68). Higher scores indicate greater pain and stiffness and poorer physical function.
postoperative first day, postoperative 4th week
World Health Organization Quality of Life-Bref
Tidsramme: postoperative first day, postoperative 4th week
The World Health Organization Quality of Life-Bref (WHOQOL-BREF) is used for general perceived quality of life. The WHOQOL-BREF consists of 26 items assessing general perceived quality of life across physical, psychological, social, environmental, and national environment domains. Each domain is scored separately on a scale up to 20 or 100, with higher scores reflecting better quality of life.
postoperative first day, postoperative 4th week
Perceived pain intensity
Tidsramme: postoperative first day, postoperative 4th week
Pain intensity was assessed using the Visual Analog Scale (VAS). The VAS was used to evaluate pain at rest, during sleep/night, and while walking. The scale consists of a 10-cm horizontal line, with 0 indicating "no pain" and 10 representing "the worst pain imaginable." Participants were asked to mark point that best described their pain, and the distance from the 0 point was measured in centimeters.
postoperative first day, postoperative 4th week
Activities of Daily Living
Tidsramme: postoperative first day, postoperative 4th week
The Lawton-Brody Instrumental Activities of Daily Living (IADL) scale assesses individuals' ability to perform instrumental daily activities. Scores range from 0-8 (dependent), 9-16 (partially dependent), and 17-24 (independent).
postoperative first day, postoperative 4th week

Samarbejdspartnere og efterforskere

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

Sponsor

Pamukkale University

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)

22. marts 2024

Primær færdiggørelse (Faktiske)

10. december 2024

Studieafslutning (Faktiske)

14. februar 2025

Datoer for studieregistrering

Først indsendt

11. januar 2026

Først indsendt, der opfyldte QC-kriterier

21. maj 2026

Først opslået (Faktiske)

22. maj 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

22. maj 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

21. maj 2026

Sidst verificeret

1. oktober 2025

Mere information

Begreber relateret til denne undersøgelse

Nøgleord

Andre undersøgelses-id-numre

  • E-60116787-020-526536

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 .

Kliniske forsøg med Total hoftearthroplastik (THA)

Kliniske forsøg med Online Education

Søg i lignende forsøg

Sponsorer og samarbejdspartnere

Medicinske tilstande

Narkotikainterventioner

CROs by country

CROs in Kenya

Betingelser

Sjældne sygdomme

Narkotikainterventioner

Kosttilskud

Sponsor / samarbejdspartnere

Placeringer

Abonner