- ICH GCP
- Yhdysvaltain kliinisten tutkimusten rekisteri
- Kliininen tutkimus NCT07650175
Balance, Fall Risk, and Gait in Women With Total Knee Arthroplasty
Investigation of Balance, Fall Risk, Gait Performance, and Quality of Life in Postmenopausal Women Undergoing Total Knee Arthroplasty
Total knee arthroplasty (TKA) is a commonly performed surgical procedure aimed at reducing pain, restoring joint function, and improving quality of life, particularly among older women. Despite improvements in pain and functional outcomes following TKA, findings regarding balance, fall risk, and gait performance remain inconsistent. Impairments in these parameters may adversely affect daily activities, independence, and overall quality of life.
Unlike previous studies that have primarily focused on one or two outcomes, this study will comprehensively evaluate balance, fall risk, gait performance, and quality of life in postmenopausal women who have undergone TKA. The findings are expected to provide a more holistic understanding of long-term functional outcomes following TKA and contribute to the planning of rehabilitation programs. Therefore, the aim of this study is to compare balance, fall risk, gait performance, and quality of life between postmenopausal women who have undergone TKA and healthy postmenopausal women.
Tutkimuksen yleiskatsaus
Tila
Ehdot
Interventio / Hoito
Yksityiskohtainen kuvaus
Total knee arthroplasty (TKA) is one of the most frequently performed surgeries aimed at reducing pain, restoring limb function and alignment, enabling normal joint movement, and increasing the level of independence in daily living activities. TKA is frequently performed in women aged 65-84 years.
In recent years, advancements in surgical techniques and prosthetic technology, along with increased surgeon experience, have broadened the range of indications for this surgery. Following TKA, balance, fall risk, and walking performance in patients can negatively impact their daily living activities and quality of life, preventing the achievement of expected rehabilitation results. While reports indicate a reduction in complaints and an increase in functional level and quality of life after TKA surgery, clear conclusions regarding patients' balance, fall risk, and walking performance have not been reached. This study differs from other studies in the literature by comprehensively evaluating the effects of TKA on critical functional parameters such as balance, fall risk, walking performance, and quality of life in postmenopausal women. While most research focuses on the effect of TDA on only one or two parameters, this study will examine four key components together, providing a more holistic assessment. Evaluating these parameters, which significantly affect the success of TDA surgery, will determine the rehabilitation process and program. Furthermore, the fact that participants scored 24 points or higher on the Mini-Mental Test will increase the reliability of the results by providing a sample capable of cognitive assessment. The aim of this study is to compare the effects of TDA surgery on balance skills, gait performance, fall risk, and quality of life in postmenopausal women who have and have not undergone the procedure.
Opintotyyppi
Ilmoittautuminen (Arvioitu)
Yhteystiedot ja paikat
Opiskeluyhteys
- Nimi: Nurcan Contarli, Doctor
- Puhelinnumero: +90 370 418 9171
- Sähköposti: nurcancontarli@karabuk.edu.tr
Osallistumiskriteerit
Kelpoisuusvaatimukset
Opintokelpoiset iät
- Aikuinen
- Vanhempi Aikuinen
Hyväksyy terveitä vapaaehtoisia
Näytteenottomenetelmä
Tutkimusväestö
Kuvaus
Inclusion Criteria:
- Volunteering to participate in the study.
- Being 60 years of age or older.
- Having a Mini Mental Test score of 24 or higher.
- Not having undergone previous arthroplasty surgery on the knee where surgery is planned.
- Having experienced unilateral TDA.
- Being a postmenopausal woman
Exclusion Criteria:
- Individuals whose vital signs are unstable after surgery, or who develop any major complications such as deep vein thrombosis, pulmonary embolism, wound infection, or prolonged anesthesia side effects.
- Presence of any neurological, vestibular, visual, cardiopulmonary, auditory, or cognitive deficits that may affect measurements.
- Individuals diagnosed with diabetes.
Opintosuunnitelma
Miten tutkimus on suunniteltu?
Suunnittelun yksityiskohdat
Kohortit ja interventiot
Ryhmä/Kohortti |
Interventio / Hoito |
|---|---|
|
control group
not having undergone TKA
|
having undergone TKA
|
Mitä tutkimuksessa mitataan?
Ensisijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
|
Single Leg Standing Test
Aikaikkuna: 1 day
|
Single Leg Standing (SLJ) Test: Balance assessment will be performed using the single leg standing (SLJ) test.
In the SLJ test, participants will be asked to stand with their extremities on the side that has not undergone surgery raised.
The duration of the test in this position will be recorded.
If the participant completes this position for 30 seconds, the test will be recorded as successful.
Sarac et al. determined the validity and reliability of the SLJ test in TDA patients as an intraclass correlation coefficient [ICC]=0.74
(0.48-0.87).
|
1 day
|
|
30-Second Sit-to-Stand Test
Aikaikkuna: 1 day
|
For the test, the individual sits in the middle of a chair without armrests, with a seat height of 43.18 cm, with their back straight, arms crossed over their chest, and feet flat on the floor.
Upon the "Start" command, they rise from the chair without pushing off with their arms, stand upright, and then sit down again.
Prior to the evaluation, the individual is assessed for two sit-to-stand repetitions to ensure they have learned the procedure.
The number of correct standing repetitions within 30 seconds is recorded as the test value.
|
1 day
|
|
Timed Up and Walk Test
Aikaikkuna: 1 day
|
The individual is asked to stand up from a chair, walk 3 meters at a safe and normal pace, turn around, walk back, and sit back down in the chair.
The time is recorded in seconds.
The test will be initiated with the patient's feet flat on the floor and their arms resting on the armrests of the chair.
Three repetitions will be performed, and the best result will be recorded.
|
1 day
|
|
10-Meter Walking Test
Aikaikkuna: 1 day
|
The 10-meter walking test will be used to assess walking ability.
In this test, the individual will be asked to walk at their normal pace in a pre-measured 10-meter area (with or without walking aids).
The timer will start when the individual's foot is on the starting line and end when they cross the finish line.
Two measurements will be taken, and the best value will be recorded in meters per second (m/s).
|
1 day
|
|
Oxford Knee Score
Aikaikkuna: 1 day
|
It is a scale developed in 1998 to investigate pain and functional status in individuals with knee replacement, and its validity and reliability have been proven (47).
The validity and reliability of the score in Turkish was proven by the research conducted by Tugay et al. in 2016 (48).
The Oxford knee score is a score consisting of 12 questions that include the problems the individual has experienced in their knee in the last 4 weeks.
The questions will be answered by individuals choosing the most appropriate situation for themselves from 5 answers related to each question.
The answers given will be scored from 0-4 and the results will be totaled.
The raw score is a value between 0-48.
|
1 day
|
Yhteistyökumppanit ja tutkijat
Sponsori
Opintojen ennätyspäivät
Opi tärkeimmät päivämäärät
Opiskelun aloitus (Arvioitu)
Ensisijainen valmistuminen (Arvioitu)
Opintojen valmistuminen (Arvioitu)
Opintoihin ilmoittautumispäivät
Ensimmäinen lähetetty
Ensimmäinen toimitettu, joka täytti QC-kriteerit
Ensimmäinen Lähetetty (Todellinen)
Tutkimustietojen päivitykset
Viimeisin päivitys julkaistu (Todellinen)
Viimeisin lähetetty päivitys, joka täytti QC-kriteerit
Viimeksi vahvistettu
Lisää tietoa
Tähän tutkimukseen liittyvät termit
Muut tutkimustunnusnumerot
- KBU-FTR-NC-11
Yksittäisten osallistujien tietojen suunnitelma (IPD)
Aiotko jakaa yksittäisten osallistujien tietoja (IPD)?
IPD-suunnitelman kuvaus
Lääke- ja laitetiedot, tutkimusasiakirjat
Tutkii yhdysvaltalaista FDA sääntelemää lääkevalmistetta
Tutkii yhdysvaltalaista FDA sääntelemää laitetuotetta
Nämä tiedot haettiin suoraan verkkosivustolta clinicaltrials.gov ilman muutoksia. Jos sinulla on pyyntöjä muuttaa, poistaa tai päivittää tutkimustietojasi, ota yhteyttä register@clinicaltrials.gov. Heti kun muutos on otettu käyttöön osoitteessa clinicaltrials.gov, se päivitetään automaattisesti myös verkkosivustollemme .
Kliiniset tutkimukset Täydellinen polven artroplastia
-
University of PennsylvaniaLopetettuRevision Total Knee ArthroplastyYhdysvallat
-
The Methodist Hospital Research InstituteEi vielä rekrytointiaRevision Total Knee Arthroplasty
-
DePuy OrthopaedicsAktiivinen, ei rekrytointiRevision Total Knee ArthroplastyYhdysvallat, Alankomaat, Uusi Seelanti, Ranska, Yhdistynyt kuningaskunta, Kanada, Australia, Itävalta, Belgia, Saksa, Irlanti, Italia, Sveitsi
-
Limacorporate S.p.aRekrytointiTäydellinen polven artroplastia | Revision Total Knee ArthroplastyYhdistynyt kuningaskunta, Portugali, Slovakia
-
Sunnybrook Health Sciences CentreRekrytointiRevision Total Knee Arthroplasty | Revision Total Hip Arthroplasty (RTHA)Kanada
-
Rothman Institute OrthopaedicsTuntematonRevision Total Knee Arthroplasty | Revision Total Hip ArthroplastyYhdysvallat
-
Rush University Medical CenterMayo ClinicValmisRevision Total Knee Arthroplasty | Revision Total Hip Arthroplasty | Akuutti verenhukka anemiaYhdysvallat
-
University of AarhusOdense University Hospital; Aarhus University Hospital; Bispebjerg Hospital; Vejle Hospital ja muut yhteistyökumppanitAktiivinen, ei rekrytointiRevision Total Hip ArthroplastyTanska
-
Ain Shams UniversityValmisRevision Total Hip Arthroplasty (RTHA)
-
Smith & Nephew, Inc.ValmisJourney II BCS Total Knee SystemYhdysvallat, Belgia, Uusi Seelanti
Kliiniset tutkimukset TKA group
-
Maisonneuve-Rosemont HospitalAktiivinen, ei rekrytointiHenkilökohtainen tyytyväisyys | Genu VarumKanada
-
The University of Tennessee, KnoxvilleSmith & Nephew, Inc.ValmisPolven nivelrikko | Täydellinen polven artroplastia | PolviYhdysvallat
-
Hospices Civils de LyonValmis
-
Newton-Wellesley HospitalExactechPeruutettuTäydellinen polven artroplastiaYhdysvallat
-
Technische Universität DresdenAktiivinen, ei rekrytointiPolven nivelrikkoSaksa
-
Ewha Womans UniversityValmisNiveltulehdus | Polven artropatia | Robotiikka
-
Orthopaedic Department of General University Hospital...MicroPort Orthopedics Inc.RekrytointiNivelleikkauksen komplikaatiot | Polven artropatia | Robotti -avustettu niveltulehdus | TKA -tuloksetKreikka
-
Peking University Third HospitalValmisRobottikirurgia | Totaalinen polven antroplastiaKiina
-
Chinese University of Hong KongEi vielä rekrytointiaPolven nivelrikko | Täydellinen polven artroplastiaHong Kong
-
Mahidol UniversityValmis