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Quadriceps Exercise Before Total Knee Arthroplasty (The QUADX-1 Trial) (QUADX-1)

Primary Purpose

Osteoarthritis, Knee

Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Two knee-extension exercise sessions per week.
Four knee-extension exercise sessions per week.
Six knee-extension exercise sessions per week.
Sponsored by
Hvidovre University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Osteoarthritis, Knee focused on measuring Knee-extension exercise, Quadriceps exercise, Knee osteoarthritis, Exercise adherence, Dose-response relationship, Prehabilitation

Eligibility Criteria

50 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patient is a possible candidate for a primary TKA due to knee osteoarthritis
  • Patient is eligible for home-based quadriceps exercise
  • Patient has an age ≥ 50 years
  • Patient is a possible candidate for primary unilateral TKA, based on all the below terms:

    • Knee pain >3 (Numeric Rating Scale) in the last week
    • Kellgren-Lawrence classification grade ≥2
    • Oxford Knee Score <30
  • Patient is resident in one of the three municipalities (København, Hvidovre or Brøndby) involved in the trial
  • Patient is able to speak and understand Danish

Exclusion Criteria:

  • Exercise is contra-indicated for the patient
  • Patient has a neurological disorder
  • Patient has a diagnosed systemic disease (ASA score ≥ 3)
  • Patients with terminal illness
  • Patient has severe bone deformity demanding use of nonstandard implants
  • Weekly alcohol consumption above national recommendations (>7 units women, >14 units men)

Sites / Locations

  • Clinical Research Centre, Amager Hvidovre hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Active Comparator

Arm Label

Group 2

Group 4

Group 6

Arm Description

Two knee-extension exercise sessions per week. Each exercise session comprises a single strength training exercise; knee-extension, which is performed in 3 sets with 12 RM repetitions in each set. The knee-extension resistance training exercise is performed with an elastic exercise band.

Four knee-extension exercise sessions per week. Each exercise session comprises a single strength training exercise; knee-extension, which is performed in 3 sets with 12 RM repetitions in each set. The knee-extension resistance training exercise is performed with an elastic exercise band.

Six knee-extension exercise sessions per week. Each exercise session comprises a single strength training exercise; knee-extension, which is performed in 3 sets with 12 RM repetitions in each set. The knee-extension resistance training exercise is performed with an elastic exercise band.

Outcomes

Primary Outcome Measures

Isometric knee-extension strength at 60 degrees knee flexion measured as Nm/kg body mass
The measurement will be assessed using a computerized strength chair (Good Strength Chair, Metitur Oy, Jyvaskyla, Finland).

Secondary Outcome Measures

Isometric knee-extension strength at 60 degrees knee flexion measured as Nm/kg body mass
The measurement will be assessed using a computerized strength chair (Good Strength Chair, Metitur Oy, Jyvaskyla, Finland).
6 min walk test for distance (6MWT)
The test measures the maximal distance a participant is able to walk in six minutes between two cones placed 29 meters apart from each other.
Stair climb test (SCT)
The test measure the time (seconds) it takes to ascend and descend an 11-step flight of stairs with 16 cm step height.
Knee Osteoarthritis Outcome Score (KOOS)
The KOOS is a questionnaire with 42 questions regarding knee function.
Oxford Knee Score (OKS)
The OKS is a 12-item questionnaire regarding knee related function and pain in patients with knee OA.
Knee pain
Individual knee pain is assessed with the Numeric Rating Scale (NRS). This is an 11-point subjective pain scale ranging from 0-10 (0 indicating no pain).
Surgical status
At the 2nd outcome assessment (after the 12 weeks exercise period) the patients are asked by the outcome assessor "based on your knee symptoms in the last week would you say that you need knee surgery now?" The answer will be categorized into one of three options; 1) 'yes' I believe I need surgery now, 2) I do not know or, 3) 'no' I do not believe I need surgery now.
Exercise adherence
Adherence to the home-based single knee-extension strength exercise will be assessed with elastics exercise bands with build-in BandCizer (sensor) technology.The sensor stores data on date, time, number of sets, repetitions, tonnage (kg x repetitions), and time-under-tension (TUT). In the present trial, a patient is defined as adherent to the exercise intervention if >75% of the prescribed exercise sessions are completed.

Full Information

First Posted
October 3, 2016
Last Updated
April 19, 2022
Sponsor
Hvidovre University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02931058
Brief Title
Quadriceps Exercise Before Total Knee Arthroplasty (The QUADX-1 Trial)
Acronym
QUADX-1
Official Title
Efficacy of Pre-operative Quadriceps Strength Training on Knee-extension Strength Before and Shortly Following Total Knee Arthroplasty: A Randomized Dose-response Trial (The QUADX-1 Trial)
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Completed
Study Start Date
October 2016 (Actual)
Primary Completion Date
February 2020 (Actual)
Study Completion Date
February 25, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hvidovre University Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The trial investigates the efficacy of knee-extension exercise prior to total knee replacement. The participants are randomly allocated to one of three exercise dosages. There is no control group.
Detailed Description
Patients with end-stage knee osteoarthritis (OA) have decreased knee-extension strength and suffer from knee pain. Strengthening of the knee-extensor muscle is a key element in conservative treatment for patients with knee OA. However, the most effective exercise dosage for knee-extension strength exercise is unknown. In this trial the investigators investigate the efficacy of three different dosages of knee-extension strength exercise. Patients eligible for total knee replacement are offered home-based pre-operative knee-extension exercise and are randomly allocated to one of three exercise dosage groups. There is no control group. The knee-extension exercise is performed with an elastic exercise band mounted with sensor (BandCizer) which registers when the patients exercise, how much they exercise and how they exercise. The intervention time is 12 weeks and the primary time point of interest is after exercise/just before surgery. Secondary time points of interest are shortly after surgery and three months after surgery. The patients are given detailed exercise instruction at trial entry and hereafter they exercise unsupervised at home for 12 weeks. At week 4 and 8 they receive follow-up instruction. Both the patients who choose not to have TKA and those who do after the exercise period will be followed with annual outcome assessments as part of a follow-up cohort. Embedded in the trial is a qualitative study. Focus group interviews will be performed with the participating patients about their experienced enablers and barriers related to adherence to the home-based intervention, once the post-operative outcome assessment has been completed. Likewise, the orthopedic surgeons and physiotherapists allocated to the trial will undergo focus group interviews, once the trial is completed, to explore their experienced enablers and barriers related to administering the home-based intervention. Protocol amendments 8/2-2017: Additional protocol approved by The Danish National Committee on Biomedical Research Ethics (protocol no. 55528 and 55529). Approved protocol amendments are the following inclusion and exclusion criteria: inclusion criteria age ≥45, and exclusion criteria ASA-score ≥4. Protocol amendments 30/3-2017: Additional protocol approved by The Danish National Committee on Biomedical Research Ethics (protocol no. 57312). Approved protocol amendments are the following inclusion criteria: knee pain during the last week (NRS) ≥3, and the OKS questionnaire score has been omitted as an inclusion criteria. Protocol amendments 6/9-2017: At the third outcome assessment (at hospital discharge, 3-8 days after surgery) only the outcomes isometric knee-extensor strength, 6MWT, SCT and current knee pain are assessed. The KOOS and OKS questionnaires as well as knee pain during the last week are omitted at this end-point as they are not validated to assess acute post-operative conditions, and use a too long recall period.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoarthritis, Knee
Keywords
Knee-extension exercise, Quadriceps exercise, Knee osteoarthritis, Exercise adherence, Dose-response relationship, Prehabilitation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
140 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Group 2
Arm Type
Active Comparator
Arm Description
Two knee-extension exercise sessions per week. Each exercise session comprises a single strength training exercise; knee-extension, which is performed in 3 sets with 12 RM repetitions in each set. The knee-extension resistance training exercise is performed with an elastic exercise band.
Arm Title
Group 4
Arm Type
Active Comparator
Arm Description
Four knee-extension exercise sessions per week. Each exercise session comprises a single strength training exercise; knee-extension, which is performed in 3 sets with 12 RM repetitions in each set. The knee-extension resistance training exercise is performed with an elastic exercise band.
Arm Title
Group 6
Arm Type
Active Comparator
Arm Description
Six knee-extension exercise sessions per week. Each exercise session comprises a single strength training exercise; knee-extension, which is performed in 3 sets with 12 RM repetitions in each set. The knee-extension resistance training exercise is performed with an elastic exercise band.
Intervention Type
Other
Intervention Name(s)
Two knee-extension exercise sessions per week.
Intervention Description
Each exercise session comprises a single strength training exercise; knee-extension, which is performed in 3 sets with 12 RM repetitions in each set. The knee-extension resistance training exercise is performed with an elastic exercise band.
Intervention Type
Other
Intervention Name(s)
Four knee-extension exercise sessions per week.
Intervention Description
Each exercise session comprises a single strength training exercise; knee-extension, which is performed in 3 sets with 12 RM repetitions in each set. The knee-extension resistance training exercise is performed with an elastic exercise band.
Intervention Type
Other
Intervention Name(s)
Six knee-extension exercise sessions per week.
Intervention Description
Each exercise session comprises a single strength training exercise; knee-extension, which is performed in 3 sets with 12 RM repetitions in each set. The knee-extension resistance training exercise is performed with an elastic exercise band.
Primary Outcome Measure Information:
Title
Isometric knee-extension strength at 60 degrees knee flexion measured as Nm/kg body mass
Description
The measurement will be assessed using a computerized strength chair (Good Strength Chair, Metitur Oy, Jyvaskyla, Finland).
Time Frame
Change from 1) baseline to 2) after 12 weeks of exercise/just before surgery
Secondary Outcome Measure Information:
Title
Isometric knee-extension strength at 60 degrees knee flexion measured as Nm/kg body mass
Description
The measurement will be assessed using a computerized strength chair (Good Strength Chair, Metitur Oy, Jyvaskyla, Finland).
Time Frame
Change from 1) baseline to 3) at hospital discharge (3-8 days after surgery), and change from 1) baseline to 4) three months after surgery
Title
6 min walk test for distance (6MWT)
Description
The test measures the maximal distance a participant is able to walk in six minutes between two cones placed 29 meters apart from each other.
Time Frame
Change from 1) baseline to 2) after 12 weeks of exercise/just before surgery, and change from 1) baseline to 3) at hospital discharge (3-8 days after surgery), and change from 1) baseline to 4) three months after surgery
Title
Stair climb test (SCT)
Description
The test measure the time (seconds) it takes to ascend and descend an 11-step flight of stairs with 16 cm step height.
Time Frame
Change from 1) baseline to 2) after 12 weeks of exercise/just before surgery, and change from 1) baseline to 3) at hospital discharge (3-8 days after surgery), and change from 1) baseline to 4) three months after surgery
Title
Knee Osteoarthritis Outcome Score (KOOS)
Description
The KOOS is a questionnaire with 42 questions regarding knee function.
Time Frame
Change from 1) baseline to 2) after 12 weeks of exercise/just before surgery, and change from 1) baseline to 3) at hospital discharge (3-8 days after surgery), and change from 1) baseline to 4) three months after surgery
Title
Oxford Knee Score (OKS)
Description
The OKS is a 12-item questionnaire regarding knee related function and pain in patients with knee OA.
Time Frame
Change from 1) baseline to 2) after 12 weeks of exercise/just before surgery, and change from 1) baseline to 3) at hospital discharge (3-8 days after surgery), and change from 1) baseline to 4) three months after surgery
Title
Knee pain
Description
Individual knee pain is assessed with the Numeric Rating Scale (NRS). This is an 11-point subjective pain scale ranging from 0-10 (0 indicating no pain).
Time Frame
Change from 1) baseline to 2) after 12 weeks of exercise/just before surgery, and change from 1) baseline to 3) at hospital discharge (3-8 days after surgery), and change from 1) baseline to 4) three months after surgery
Title
Surgical status
Description
At the 2nd outcome assessment (after the 12 weeks exercise period) the patients are asked by the outcome assessor "based on your knee symptoms in the last week would you say that you need knee surgery now?" The answer will be categorized into one of three options; 1) 'yes' I believe I need surgery now, 2) I do not know or, 3) 'no' I do not believe I need surgery now.
Time Frame
Assessment at 2) after 12 weeks of exercise/just before surgery
Title
Exercise adherence
Description
Adherence to the home-based single knee-extension strength exercise will be assessed with elastics exercise bands with build-in BandCizer (sensor) technology.The sensor stores data on date, time, number of sets, repetitions, tonnage (kg x repetitions), and time-under-tension (TUT). In the present trial, a patient is defined as adherent to the exercise intervention if >75% of the prescribed exercise sessions are completed.
Time Frame
Assessment at 2) after 12 weeks of exercise/just before surgery
Other Pre-specified Outcome Measures:
Title
Adverse events
Description
All adverse events occurring while the patient is enrolled in the trial will be recorded regardless of its relation to the exercise intervention, surgery or occurrences not related to the trial.
Time Frame
Assessment at 2) after 12 weeks of exercise/just before surgery, 3) at hospital discharge (3-8 days after surgery) and 4) three months after surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient is a possible candidate for a primary TKA due to knee osteoarthritis Patient is eligible for home-based quadriceps exercise Patient has an age ≥ 50 years Patient is a possible candidate for primary unilateral TKA, based on all the below terms: Knee pain >3 (Numeric Rating Scale) in the last week Kellgren-Lawrence classification grade ≥2 Oxford Knee Score <30 Patient is resident in one of the three municipalities (København, Hvidovre or Brøndby) involved in the trial Patient is able to speak and understand Danish Exclusion Criteria: Exercise is contra-indicated for the patient Patient has a neurological disorder Patient has a diagnosed systemic disease (ASA score ≥ 3) Patients with terminal illness Patient has severe bone deformity demanding use of nonstandard implants Weekly alcohol consumption above national recommendations (>7 units women, >14 units men)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Thomas Bandholm, PhD
Organizational Affiliation
Clinical Research Center, Hvidovre University Hospital
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Rasmus S Husted, MSc., PT.
Organizational Affiliation
Clinical Research Center, Hvidovre University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Clinical Research Centre, Amager Hvidovre hospital
City
Hvidovre
ZIP/Postal Code
2650
Country
Denmark

12. IPD Sharing Statement

Plan to Share IPD
Yes
Citations:
PubMed Identifier
35413476
Citation
Husted RS, Troelsen A, Husted H, Gronfeldt BM, Thorborg K, Kallemose T, Rathleff MS, Bandholm T. Knee-extensor strength, symptoms, and need for surgery after two, four, or six exercise sessions/week using a home-based one-exercise program: a randomized dose-response trial of knee-extensor resistance exercise in patients eligible for knee replacement (the QUADX-1 trial). Osteoarthritis Cartilage. 2022 Jul;30(7):973-986. doi: 10.1016/j.joca.2022.04.001. Epub 2022 Apr 9.
Results Reference
derived
PubMed Identifier
33095777
Citation
Husted RS, Bandholm T, Rathleff MS, Troelsen A, Kirk J. Perceived facilitators and barriers among physical therapists and orthopedic surgeons to pre-operative home-based exercise with one exercise-only in patients eligible for knee replacement: A qualitative interview study nested in the QUADX-1 trial. PLoS One. 2020 Oct 23;15(10):e0241175. doi: 10.1371/journal.pone.0241175. eCollection 2020.
Results Reference
derived
PubMed Identifier
29347947
Citation
Husted RS, Troelsen A, Thorborg K, Rathleff MS, Husted H, Bandholm T. Efficacy of pre-operative quadriceps strength training on knee-extensor strength before and shortly following total knee arthroplasty: protocol for a randomized, dose-response trial (The QUADX-1 trial). Trials. 2018 Jan 18;19(1):47. doi: 10.1186/s13063-017-2366-9.
Results Reference
derived
Available IPD and Supporting Information:
Available IPD/Information Type
Study Protocol
Available IPD/Information URL
https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-017-2366-9

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Quadriceps Exercise Before Total Knee Arthroplasty (The QUADX-1 Trial)

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