Arthropathy of Knee, Knee Osteoarthritis
Conditions
Brief summary
The study was designed to test patient acceptance and system usability and to assess clinical outcomes of a home-based rehabilitation program using a novel kinematic biofeedback system in the rehabilitation after total knee replacement versus conventional rehabilitation, This system allows the patients to perform independent rehabilitation sessions at home, under remote monitoring from the clinical team. The investigators hypothesize that the system will be well received by patients and that the clinical outcomes will be at least similar those of conventional rehabilitation. This is a quasi-randomized controlled trial with active comparator. Patients will be enrolled pre-operatively and divided into 2 groups: experimental group and conventional rehabilitation group according to geographical criteria. Both groups will perform 8 weeks of rehabilitation starting between day 7 and 10 after surgery. The experimental group will perform daily rehabilitation sessions at home using the system, under remote monitoring from a physical therapist. The conventional rehabilitation group will perform 1h rehabilitation sessions 3 times a week, at home, given by a physical therapist. The following feasibility outcomes will be registered: enrollment rate, retention rate (drop-outs), compliance to the program, independence of use, need for therapist contact and patient satisfaction. Clinical outcomes will be measured at weeks 4 and 8 and then at 3 and 6 months. The primary outcome will be measured in terms of patient performance in the Timed-up-and-Go (TUG) test in comparison with the pre-operative score. Secondary outcomes will be measured in terms of: b) Knee Osteoarthritis Outcome Score); c) range of motion of the knee joint.
Interventions
The system will be used independently by the patients to perform rehabilitation sessions at home, under remote monitoring from the clinical team. A tailored rehabilitation program will be prescribed, based on the following principles: STAGE 1 (Weeks 0-2) Open kinetic chain exercises without added resistance: lying, sitting and standing (with support) Strengthening of hip flexors and extensors Ice pack application after each session and throughout the day as needed STAGE 2 (weeks 3-6) Open kinetic chain exercises with added resistance, progressing to closed kinetic chain exercises, with strengthening of knee flexors and extensors and knee stabilization Progression to standing exercises without support lying, sitting and standing (with support) Exercises with steps Ice pack application after each session and throughout the day as needed STAGE 3 (Weeks 7-8) Eccentric strengthening exercises Exercises involving steps Multi-directional exercises
Patients will perform 3 weekly rehabilitation sessions, with a duration of 1 hour, for 8 weeks, provided by a physical therapist. The rehabilitation program will respect the following principles: STAGE 1 (Weeks 0-2) Soft tissue massage Active assisted mobilisation of the knee to increase range of motion Gait training with bilateral support Open kinetic chain exercises without added resistance Strengthening of hip flexors and extensors Ice pack application STAGE 2 (weeks 3-6) Soft tissue massage Active assisted mobilisation of the knee to increase range of motion Open kinetic chain exercises with added resistance, progressing to closed kinetic chain exercises, with strengthening of knee flexors/ extensors and knee stabilisation Gait training with progressive withdrawal of external support Ice pack application STAGE 3 (Weeks 7-8) Eccentric strengthening exercises Exercises involving steps Weight-bearing exercises on uneven surfaces Ice pack application
Sponsors
Hospital da Prelada
Sword Health, SA
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)
Masking description
All patients will be assessed for clinical outcomes by an independent rater blinded to the study arm
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Patients over 18 years old * Clinical and imaging evidence of knee osteoarthritis * Indication for total knee replacement according to the patient´s orthopedic surgeon * Ability to walk unaided, with unilateral or bilateral support * Availability of a carer to assist the patient after surgery
Exclusion criteria
* Patients admitted for revision of total knee replacement * Contralateral hip or knee osteoarthritis severely limiting patient mobility and ability to comply with a rehabilitation program * Aphasia, dementia or psychiatric comorbidity interfering with the communication or compliance to the rehabilitation process * Respiratory, cardiac, metabolic or other condition incompatible with at least 30 minutes of light to moderate physical activity * Major medical complications occurring after surgery that prevent the discharge of the patient within 10 days after the surgery * Other medical and/or surgical complications that prevent the patient from complying with a rehabilitation program * Blind and/or illiterate patients
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change in the Timed up And Go Test score | Baseline; 4 and 8 weeks after initiation of rehabilitation program and then at 3 and 6 months after surgery | The timed up and go requires a patient to rise from a chair walk three meters around a piece of tape and return to the chair again as quickly as possible. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change in Knee injury and Osteoarthritis Outcome Score (KOOS) | Baseline; 4 and 8 weeks after initiation of rehabilitation program and then at 3 and 6 months after surgery | The KOOS is a standardized and validated patient outcome score that assesses functional limitation in patient with knee problems. |
| Change in Knee Range of Motion (degrees) | Baseline; 4 and 8 weeks after initiation of rehabilitation program and then at 3 and 6 months after surgery | Change in knee flexion/extension measured in degrees |
Other
| Measure | Time frame | Description |
|---|---|---|
| Compliance | For each patient, at week 8. | This will be measured by calculating the percentage of patients allocated to the experimental group that performed at least 5 weekly sessions throughout the program |
| Enrollment rate | At the end of patient enrollment- up to 18 months after trial initiation | This will be measured through the percentage of patients that actually enroll in the study after initial screening. |
| Patient Satisfaction | At week 8 or upon dropout. | This will be measured in the experimental group by answering the following question: On a scale from 0 to 10, how likely are you to recommend this intervention to a friend or neighbour?. Scores of 9 and 10 will be considered good, 7 and 8 neutral and less than 7 bad. |
| Retention rate | At week 8 | This will be assessed through the percentage of patients in the experimental group that complete the 8-week program |
| Independence of use | For each patient, at week 8 or upon dropout. | This will be assessed through the percentage of patients in the experimental group that require the assistance of a caregiver in interacting with the system. |
Countries
Portugal
Outcome results
None listed