search  
 


Home

Who are we?

Why
register?


Signup for
registration


Online registration

Log in to register
your trial


Search a trial

NRT en CCMO

Contact

NEDERLANDS





MetaRegister
van CCT (UK)


ISRCTN-Register
van CCT (UK)


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


- candidate number24294
- NTR NumberNTR5813
- ISRCTNISRCTN no longer applicable
- Date ISRCTN created
- date ISRCTN requested
- Date Registered NTR25-apr-2016
- Secondary IDsW16.072  METC MMC
- Public TitleA tailor made exercise program versus a standard exercise program in patients with chronic mid portion achillestendinopathy
- Scientific TitleComparing 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
- ACRONYM
- hypothesisOur hypothesis is that our gradually progressive protocol offers advantages with respect to the eccentric protocol based on the protocol of Alfredson (gold standard). We expect that, because this protocol is more individualized, less pain during the execution of the exercise program, therefore there is a better compliance and, and there is less chance of a deteriotaration of the tendon capacity (better clinical function).
- Healt Condition(s) or Problem(s) studiedAchilles tendinopathy, Exercise therapy
- Inclusion criteriaAge 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 criteriaInsertional 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).
- mec approval receivedno
- multicenter trialno
- randomisedyes
- masking/blindingSingle
- controlActive
- groupParallel
- Type2 or more arms, randomized
- Studytypeintervention
- planned startdate 1-aug-2016
- planned closingdate31-dec-2017
- Target number of participants66
- Interventions1. tailor made, slowly progressive exercise program, guided by clincal parameters
2. standard eccentric exercise program;
- Primary outcomePatient satisfaction
Functional outcome (VISA-A)
- Secondary outcomePain relief after exercise during the first 4 weeks
Achievement of the treatment goal (defined by the patient)
Compliance
Patient Satisfaction
- Timepoints0 weeks (T0; intake)
4 weeks (T1)
16 weeks (T2)
24 weeks (T3)
36 weeks (T4)
52 weeks (T5)
- Trial web sitenot applicable
- statusplanned
- CONTACT FOR PUBLIC QUERIES M.A.W. Breuer
- CONTACT for SCIENTIFIC QUERIES M.A.W. Breuer
- Sponsor/Initiator Máxima Medical Center
- Funding
(Source(s) of Monetary or Material Support)
Maxima Medical Center
- Publicationsnot applicable
- Brief summarynot applicable
- Main changes (audit trail)
- RECORD25-apr-2016 - 22-jun-2016


  • Indien u gegevens wilt toevoegen of veranderen, kunt u een mail sturen naar nederlands@trialregister.nl