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Effect of shoe adaptation on pain and ankle motion in patients with post traumatic ankle arthritis

Effect of shoe adaptation on pain and ankle motion in patients with post traumatic ankle arthritis - Shoe adaptation in post traumatic ankle arthritis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON40032
Enrollment
32
Registered
2013-06-05
Start date
2013-08-19
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

posttraumatic artritis

Interventions

The intervention shoe, referred to as type B, is a standard shoe, of the brand Dr. Comfort, but modified with a proximally placed fulcrum, sole stiffening and a rounded heel, hereafter called togeth

Sponsors

Universitair Medisch Centrum Groningen
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: For the patient group: 1. Age >= 18 years 2. Fracture of tibia, fibula or talus in medical history 3. Daily ankle and/or foot pain with a VAS score at baseline > 3 4. Radiological evidence for osteoarthritis in tibial-talar joint 5. Being able to walk at least 100 meters without any support 6. Signed Informed Consent;For the healthy volunteers: 1. Age >= 18 years 2. Signed Informed Consent

Exclusion criteria

Exclusion criteria: For the patient group: 1. Concomitant conditions like cardiovascular disease or neuromuscular disease or musculo-skeletal problems in other joints that intervene with walking 2. Ankle arthrodesis or arthroplasty in place 3. Other forms of osteoarthritis (e.g. primary osteoarthritis, OA secondary to rheumatoid arthritis or haemophilia) 4. Leg length difference of more than 2 cm 5. Planned activities within the research period, like holiday, that influence the normal level of avtivity 6. Limited ankle motion in rest, defined as total passive ROM (range of motion)

Design outcomes

Primary

MeasureTime frame
Primary biomechanical outcome: Range of Motion (the maximum motion in ankle joint) during stance phase. Priamry clinical outcome: Pain (daily average) around the ankle measured through Visual Analogue Scale (VAS) .

Secondary

MeasureTime frame
Secondary biomechenical outcomes: Joint moments of ankle and knee Step rate/lenght and stance time Secondary clinical outcome: Pain (daily maximum) around the ankle measured through Visual Analogue Scale (VAS) .

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)