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Can Targeted Exercise Improve Knee Strength Following ACLR (RATE) (RATE)

Primary Purpose

Rupture of Anterior Cruciate Ligament, Muscle Degeneration, Gait, Unsteady

Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Targeted exercise
Sponsored by
University of Southern Denmark
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Rupture of Anterior Cruciate Ligament

Eligibility Criteria

18 Years - 40 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age between 18-40 years,
  • ACL-reconstructed using hamstring tendon auto-grafts, and a pathological defined between limb asymmetry ratio (operated/non-operated) of more than 10 % for maximal isometric strength of the knee flexors, at 1 year follow-up.

Exclusion Criteria:

  • Other known pathology conditions in hip, knee, or ankle,
  • BMI above 35, and
  • Not understanding written Danish language.

Sites / Locations

  • Orthopaedic Research Unit, Institute of Clinical Research, SDU

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

No Intervention

Arm Label

Targeted exercise

care as usual

Arm Description

Targeted exercise intervention

home based exercises

Outcomes

Primary Outcome Measures

Change in isometric maximal knee flexor muscle strength
Change, pre- and post intervention using stabilized maximal isometric dynamometry (in Nm)

Secondary Outcome Measures

Change in isometric knee extensor strength
Change, pre- and post intervention using stabilized maximal isometric dynamometry (in Nm)
Change in isometric maximal hamstring to quadriceps strength ratio
Change, pre- and post intervention using stabilized maximal isometric dynamometry (in percentage)
Change in Self-perceived knee related function
Change, pre- and post intervention, using Patient reported outcomes (PROM) questionnaires (KOOS, Knee injury and Osteoarthritis Outcome Score, all subscales)

Full Information

First Posted
October 4, 2016
Last Updated
December 22, 2020
Sponsor
University of Southern Denmark
Collaborators
Odense University Hospital, Kolding Sygehus
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1. Study Identification

Unique Protocol Identification Number
NCT02939677
Brief Title
Can Targeted Exercise Improve Knee Strength Following ACLR (RATE)
Acronym
RATE
Official Title
Can Targeted Exercise Improve Knee Strength in Patients With Persisting Hamstring Deficiency Following ACL-reconstruction? - A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
December 2020
Overall Recruitment Status
Completed
Study Start Date
January 2017 (undefined)
Primary Completion Date
December 2020 (Actual)
Study Completion Date
December 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Southern Denmark
Collaborators
Odense University Hospital, Kolding Sygehus

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Anterior cruciate ligament reconstruction (ACLR) is high volume surgery, carried out in about 2800 patients annually in Denmark per year. ACLR patients (using hamstring auto-graft) have persistent hamstring strength deficiency when evaluated more than 1-2 years after ACL-reconstruction. The investigators have designed this randomized controlled trial (RCT) with the main purpose to investigate the effect of a targeted muscle strength exercise intervention on the neuromuscular rehabilitation of ACLR-patients compared with 'care-as- usual'. The study is designed as a prospective, superiority, parallel-group with balanced randomization (1:1) RCT (Level of evidence: II) with blinded allocation, and outcome assessment according to the CONSORT statement (Consolidated Standards of Reporting Trials). 50 patients with ACL reconstruction and persistent hamstring muscle deficiency, will be recruited at the outpatient clinic 1-year follow-up, and allocated to one of two 12 weeks' interventions, either a) the supervised progressive strength and neuromuscular exercise group (SNG) with supervised training twice weekly. Or b) the control group (CON) receiving patient education based on a home-based exercise regime of low intensity, defined as 'care as usual'. Outcome measures include, maximal isometric knee flexor muscle strength (primary outcome), knee extensor strength, and the Knee injury and Osteoarthritis Outcome Score (KOOS) (secondary outcomes). In addition, the following explorative outcomes will be investigated; hamstring to quadriceps strength ratios, the International Knee Documentation Committee Subjective Knee Form (IKDC), magnetic resonance imaging (MRI) to evaluate tendon regeneration of the hamstrings and finally kinetic/kinematic biomechanical outcomes of knee related functional tasks. To the investigators knowledge, this is the first RCT to investigate the efficacy of combined progressive resistance training and neuromuscular exercise in the late rehabilitation phase in patients demonstrating persistent limb-to-limb knee muscle asymmetry following ACLR. Reduced hamstring strength represents a potential risk factor for secondary ligament rupture and accelerated progression of osteoarthritis (OA). If deemed effective, the intervention paradigm introduced in this study may help to improve current treatment strategies.
Detailed Description
Detailed study description available in the published study protocol: "The effect of targeted exercise on kneemuscle function in patients with persistent hamstring deficiency following ACL reconstruction - study protocol for a randomized controlled trial". Bo Bregenhof1,3* , Uffe Jørgensen1, Per Aagaard2, Nis Nissen3, Mark W. Creaby4, Jonas Bloch Thorlund2, Carsten Jensen3, Trine Torfing5 and Anders Holsgaard-Larsen1 Published: Trials. 2018; 19: 75. Published online 2018 Jan 26. doi: 10.1186/s13063-018-2448-3

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rupture of Anterior Cruciate Ligament, Muscle Degeneration, Gait, Unsteady

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
51 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Targeted exercise
Arm Type
Other
Arm Description
Targeted exercise intervention
Arm Title
care as usual
Arm Type
No Intervention
Arm Description
home based exercises
Intervention Type
Other
Intervention Name(s)
Targeted exercise
Intervention Description
12 weeks of targeted and supervised exercise intervention vs. "care as usual" (home based exercises)
Primary Outcome Measure Information:
Title
Change in isometric maximal knee flexor muscle strength
Description
Change, pre- and post intervention using stabilized maximal isometric dynamometry (in Nm)
Time Frame
12 weeks (intervention period)
Secondary Outcome Measure Information:
Title
Change in isometric knee extensor strength
Description
Change, pre- and post intervention using stabilized maximal isometric dynamometry (in Nm)
Time Frame
12 weeks (intervention period)
Title
Change in isometric maximal hamstring to quadriceps strength ratio
Description
Change, pre- and post intervention using stabilized maximal isometric dynamometry (in percentage)
Time Frame
12 weeks (intervention period)
Title
Change in Self-perceived knee related function
Description
Change, pre- and post intervention, using Patient reported outcomes (PROM) questionnaires (KOOS, Knee injury and Osteoarthritis Outcome Score, all subscales)
Time Frame
12 weeks (intervention period)
Other Pre-specified Outcome Measures:
Title
Gait analysis
Description
Change, pre- and post intervention (12 weeks) using 3-dimensional Vicon motion analysis
Time Frame
12 weeks (intervention period)
Title
Counter movement jump
Description
Change, pre- and post intervention (12 weeks) using 3-dimensional Vicon motion analysis (force Development)
Time Frame
12 week intervention period
Title
Change in One-leg jump for distance
Description
Change, pre- and post intervention (12 weeks) in jumping distance (in cm). Simple functional test.
Time Frame
12 week intervention period
Title
Change in Quadriceps and hamstring morphologies
Description
Change, pre- and post intervention (12 weeks) concerning volume, peak cross sectional area and length of muscle and tendon, using Magnetic resonance imaging (MRI)
Time Frame
12 week intervention period
Title
Change in Rate of force Development (RFD) in maximal quadriceps and hamstring strenght
Description
Change, pre- and post intervention (12 weeks) using maximal isometric dynamometry (Nm/millisecond)
Time Frame
12 week intervention period
Title
Change in Self-perceived knee related function and symptoms
Description
Change, pre- and post intervention (12 weeks) using Patient reported outcomes (PROM) questionnaires (IKDC, subjective knee evaluation form)
Time Frame
12 week intervention period

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age between 18-40 years, ACL-reconstructed using hamstring tendon auto-grafts, and a pathological defined between limb asymmetry ratio (operated/non-operated) of more than 10 % for maximal isometric strength of the knee flexors, at 1 year follow-up. Exclusion Criteria: Other known pathology conditions in hip, knee, or ankle, BMI above 35, and Not understanding written Danish language.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anders Holsgaard-Larsen, ass.proff
Organizational Affiliation
Orthopaedic Research Unit, Institute of Clinical Research, SDU
Official's Role
Study Director
Facility Information:
Facility Name
Orthopaedic Research Unit, Institute of Clinical Research, SDU
City
Odense
State/Province
Region Of Southern Denmark
ZIP/Postal Code
5000
Country
Denmark

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
29373984
Citation
Bregenhof B, Jorgensen U, Aagaard P, Nissen N, Creaby MW, Thorlund JB, Jensen C, Torfing T, Holsgaard-Larsen A. The effect of targeted exercise on knee-muscle function in patients with persistent hamstring deficiency following ACL reconstruction - study protocol for a randomized controlled trial. Trials. 2018 Jan 26;19(1):75. doi: 10.1186/s13063-018-2448-3.
Results Reference
derived

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Can Targeted Exercise Improve Knee Strength Following ACLR (RATE)

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