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Home Based Hip Strengthening for Knee OA Patients

11. november 2021 opdateret af: Faizan Asghar, University of Lahore

Effects of Home-based Hip Strengthening Exercises on Pain, Range of Motion and Functional Disability in Knee Osteoarthritis Patients: a Randomized Controlled Trial

In knee osteoarthritis patients, weakness of hip abductor muscles is considered an important contributing factor leading to the progression of the disease.

Studieoversigt

Status

Ikke rekrutterer endnu

Betingelser

Detaljeret beskrivelse

Osteoarthritis is the most common type of disease that results from an abnormality in joint function. Osteoarthritis(OA) is a condition that is characterized by progressive loss of articular cartilage of a joint and causes pain. Yamda et al. found that the strength of hip adductors increases with the severity of the disease. This reflects that more use of these muscles lower knee adductor moment 54. Considering this research, knee loads can be altered by strengthening hip muscles. Pakistan is listed in 3rd world countries and the poverty index is high. Many patients show reluctance in going to clinics for the physiotherapeutic management of knee OA. So, the present research intends to investigate the effects of home-based hip strengthening exercise on pain, functions, and range of motion in elderly knee osteoarthritis patients.

Undersøgelsestype

Interventionel

Tilmelding (Forventet)

90

Fase

  • Ikke anvendelig

Kontakter og lokationer

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

Studiekontakt

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

40 år til 60 år (Voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  • The age group was from 40 to 60 years.
  • Both males and females were included.
  • Average knee pain on walking >3 on an 11-point scale (NPRS) (0 no pain; 10 maximal pain).
  • participants can walk independently without any assistive devices
  • Diagnosed patients of grade II & III of Kallgren and Lawrence scale for knee osteoarthritis referred by an orthopaedic surgeon

Exclusion Criteria:

  • History of osteoporosis.
  • Leg length discrepancy or structural deformity
  • Knee surgery or TKR.
  • Corticosteroid injection in knee joint
  • Systemic arthritic condition
  • History of tibiofemoral and patellofemoral replacement
  • Any other neurological and muscular condition affecting the lower limb
  • Any history of radiculopathy.

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: Dobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Aktiv komparator: Conventional group

Patients will be given thermal therapy with the hot pack for 20 minutes followed by Conventional physiotherapy will consist of a set of exercises. The exercise components willl be chosen based on previous studies (Deyle 2000) and will comprises of

  • stretches of lower limb muscles (gastrocnemius, soleus and hamstring)
  • isometric quadriceps work
  • straight leg raising
  • Joint mobilization includes anteroposterior (AP) glide of the tibia on the femur
  • the patella glides in all directions Subjects will participate in a 45-minute physical therapy session, on alternate days weekly for 6 weeks, in our centre under the close surveillance of a physical therapist. A total of 24 sessions will be given to this group.
this group will perform conventional therapy
Eksperimentel: interventional group

Patients in this group will perform home-based hip Strengthening exercises to strengthen hip abductor and adductor muscles. Six different home-based exercises will be taught. This group will have 3 sessions in 1st week in the hospital under the supervision of a trained physiotherapist just to teach them and ensure that patients are doing exercises correctly on their own. After that, patients will perform exercises 5 days at home and 1 session at the hospital per week. The therapist will be trained to deliver different exercises and adjust the intensity of exercise accordingly advise the participants to complete 10 repetitions of every exercise at home96.

  • Abduction in side-lying
  • Abduction in standing
  • Standing wall isometric hip abduction
  • Hip Adduction in side-lying
  • Hip abduction in a standing position
  • Towel press
this group will perform home based exercises

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
intensity of Pain
Tidsramme: baseline data
The numerical Pain Rating Scale will be used to measure pain.
baseline data
intensity of Pain
Tidsramme: at the end of 6th week
The numerical Pain Rating Scale will be used to measure pain.
at the end of 6th week
Range of Motion
Tidsramme: baseline data
A goniometer will be used to measure a range of motion.
baseline data
Range of Motion
Tidsramme: at the end of 6th week
A goniometer will be used to measure a range of motion.
at the end of 6th week
Functional Disability
Tidsramme: baseline data
KOOS Scale will be used to measure functional disability.
baseline data
Functional Disability
Tidsramme: at the end of 6th week
KOOS Scale will be used to measure functional disability.
at the end of 6th week

Samarbejdspartnere og efterforskere

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

Efterforskere

  • Ledende efterforsker: faizan asghar, The University of Lahore

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 (Forventet)

1. november 2021

Primær færdiggørelse (Forventet)

1. december 2021

Studieafslutning (Forventet)

1. januar 2022

Datoer for studieregistrering

Først indsendt

11. november 2021

Først indsendt, der opfyldte QC-kriterier

11. november 2021

Først opslået (Faktiske)

23. november 2021

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

23. november 2021

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

11. november 2021

Sidst verificeret

1. november 2021

Mere information

Begreber relateret til denne undersøgelse

Plan for individuelle deltagerdata (IPD)

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