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Eccentric resistance ergometry in knee osteoarthritis rehabilitation: a randomized clinical trial

The effects of adding eccentric ergometry to standard physiotherapy management on quadriceps strength and physical function in individuals with knee osteoarthritis: a randomized clinical study.

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12612000411842
Acronym
EUREKA
Enrollment
80
Registered
2012-04-12
Start date
2012-04-15
Completion date
Unknown
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

The primary aim of this randomized controlled trial (RCT) is to compare the symptomatic and biomechanical effects of standard Physiotherapy treatment with the addition of eccentric ergometry with those of standard Physiotherapy treatment with concentric ergometry in people with symptomatic medial tibiofemoral OA

Interventions

Patients randomized to the intervention arm would receive standard physiotherapy treatment and they will exercise on an eccentric ergometer. Both Physiotherapy and ergometry training will be delivered individually. Standard physiotherapy treatment would be delivered by experienced Physiotherapists. Specifically, the standard Physiotherapy treatment comprises a combination of manual therapy and therapeutic exercises. For the manual therapy component, the techniques chosen comprise passive physiol

Patients randomized to the intervention arm would receive standard physiotherapy treatment and they will exercise on an eccentric ergometer. Both Physiotherapy and ergometry training will be delivered individually. Standard physiotherapy treatment would be delivered by experienced Physiotherapists. Specifically, the standard Physiotherapy treatment comprises a combination of manual therapy and therapeutic exercises. For the manual therapy component, the techniques chosen comprise passive physiological and accessory movements, muscle stretching, and soft tissue mobilization. These techniques will be applied by the treating physiotherapists in accordance to their assessment findings. For the therapeutic-exercises component, the exercises will be supervised by the treating physiotherapists and the exercises consist of (i) active range-of-motion exercises, (ii) muscle strengthening exercises, and (iii) balance and functional training. All manual therapy techniques and therapeutic exercises would be progressed only if the symptoms and signs of OA (pain, knee effusion, and muscle soreness) are decreasing. Eccentric ergometry training involves cycling on an eccentric ergometer. Exercise intensity will be determined by the Borg’s rating of perceived exertion (RPE) scale. Dosage will be 15 minutes per session. In the absence of increased knee pain, effusion, or excessive fatigue, the patients are allowed to gradually progress from an initial RPE rating of "very very light intensity" on the first session to an RPE rating of “hard intensity" in the subsequent sessions. Physiotherapy treatment will be delivered twice weekly for the first 3 weeks and once weekly for the next 5 weeks. Each treatment session is 30mins in duration. Patients will train twice weekly on the eccentric ergometer and each session is 15mins in duration.

Sponsors

Singapore General Hospital
Lead SponsorHospital

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
50 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

(i) Patients with primary medial tibiofemoral OA (ii) Knee flexion range of motion greater or equal to 100 degrees

Exclusion criteria

(1) Patellofemoral joint symptoms overshadowing tibiofemoral symptoms, as determined from clinical examination (2) Current or past (within 4 weeks) oral corticosteroid use; (3) Systemic arthritic conditions; (4) A previous history of hip or knee joint replacement or tibial osteotomy (5i) Inability to ambulate 10 metres without a gait aid.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026