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A tailor made exercise program versus a standard exercise program in patients with chronic mid portion achillestendinopathy

Comparing a patient-specific, gradually progressive exercise program guided by clinical parameters with a standard eccentric exercise program in people with chronic mid portion achillestendinopathy; a randomized trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON21627
Enrollment
66
Registered
2016-04-25
Start date
2016-08-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Achillestendinopathy Achillestendinopathie Mid portion Achillestendinopathy Mid portion Achillestendinopathie Exercise therapy Oefentherapie Eccentric exercise Excentrische oefeningen Isometric exercise Isometrische oefeningen Pain Pijn Function Functie VISA-A score Compliance Therapietrouw

Interventions

1. tailor made, slowly progressive exercise program, guided by clincal parameters 2. standard eccentric exercise program

Sponsors

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Age 18 years or older; Clinical diagnosis (based on history and physical examination) of midportion Achillestendinopathy (the 2-7 cm proximal to the insertion on the calcaneus); Duration of symptoms 3 months or more

Exclusion criteria

Exclusion criteria: Insertional tendinopathy of the Achilles tendon; Not able to carry out 'heavy load' eccentric exercises; clinically suspected diagnosis of acute (partial) rupture of the Achilles tendon; Surgical treatment of the affected Achilles tendon in the past; Systemic disorders that seriously can influence the treatment/prognosis (diabetes mellitus, rheumatoid artritis).

Design outcomes

Primary

MeasureTime frame
Patient satisfaction Functional outcome (VISA-A)

Secondary

MeasureTime frame
Pain relief after exercise during the first 4 weeks Achievement of the treatment goal (defined by the patient) Compliance Patient Satisfaction

Contacts

Public ContactM.A.W. Breuer

De Run 4600

e-mail: m.breuer@mmc.nlTel. (040) 888 60 40

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)