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Trial registered on ANZCTR
Registration number
ACTRN12622000160730
Ethics application status
Approved
Date submitted
20/10/2021
Date registered
31/01/2022
Date last updated
30/01/2023
Date data sharing statement initially provided
31/01/2022
Type of registration
Prospectively registered
Titles & IDs
Public title
Effects of specific closed kinematic chain excercises with biofeedback assissted position control and against forces enhancing positional disorder on lower limb movement pattern
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Scientific title
Effects of closed kinematic chain exercises with active auto-correction of artificially enhanced disorders of the lower limbs positioning on their movement pattern in adults
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Secondary ID [1]
305594
0
None
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Functional disturbances of Lower limbs axis
324021
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Condition category
Condition code
Musculoskeletal
321528
321528
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0
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Other muscular and skeletal disorders
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Physical Medicine / Rehabilitation
322129
322129
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0
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Physiotherapy
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Interventions is basically an exercises with resistance of the lower limbs in closed biokinematic chains, performed with modified "Leg-press" device. This kind of device allows only movement of extension and flexion of lower limbs against resistance - in this specific device (TELKO, manufactured/ distributed byACX/Technomex, Poland) resistance is created from elastic tubing. The only exercise performed will be flexion/ extension of lower limbs in closed kinematic chain made simultaneously for both limbs. The device uses virtual reality visual games to maintain patient focus in training and control parameters like force distribution between left/ right leg. The modification from standard training is due to active correction of the position of the feet and the axis of the lower limbs performed by the strength of the patient's own muscles, against the force disturbing this setting towards the valgus of the knees. The disturbing force will be realized through an elastic band (medium strength). The control of the position of the feet and the axis of the lower limbs will be performed with the use of biofeedback phenomenon and additional controls ( two on upper lowel leg, responsible for lower legs axis, and two on foot, responsible for keeping correct position / pressure of the foot).
The exercises will last 15 minutes daily, with resistance and fatigue desribed by the patient as moderate to heavy but pleasant (3 to 5 in ten point Borg Scale). This exercise will be performed individually, as we have only one such device.
As every participant will have individual account on the device software, report from every training session will be recorded and used for control of attendance and participation in training session.
Speed of excercise - according to patient possibilities, but with instructions that primary goal is to perform the exercise correctly (according to attached controls described above) not speed or fatigue.
Excercises will be performed for 5 days between the initial and final assessment - to avoid effects of muscle strengtening, instead of motor contol effect.
Intervention will be delivered by Physiotherapist with active right to physiotherapy practice.
The research will be held at "Pod Tezniami" Health Resort and Physiotherapy center in Ciechocinek, Poland.
All patients will receive the patient's informed consent form to participate in the research, they will be informed in detail about the course of the research and that they can resign from participation at any time.
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Intervention code [1]
321993
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Rehabilitation
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Comparator / control treatment
Interventions is basically an exercises with resistance of the lower limbs in closed biokinematic chains, performed with modified "Leg-press" device. This kind of device allows only movement of extension and flexion of lower limbs against resistance - in this specific device (TELKO, manufactured/ distributed byACX/Technomex, Poland) resistance is created from elastic tubing. The only exercise performed will be flexion/ extension of lower limbs in closed kinematic chain made simultaneously for both limbs. The device uses virtual reality visual games to maintain patient focus in training and control parameters like force distribution between left/ right leg. Exercise will be conducted without modifications described for research group.
The exercises will last 15 minutes daily, with resistance and fatigue desribed by the patient as moderate to heavy but pleasant (3 to 5 in ten point Borg Scale). This exercise will be performed individually, as we have only one such device.
As every participant will have individual account on the device software, report from every training session will be recorded and used for control of attendance and participation in training session.
Speed of excercise - according to patient possibilities, but with instructions that primary goal is to perform the exercise correctly by patient own visual observation of lower limb axis
Excercises will be performed for 5 days between the initial and final assessment - to avoid effects of muscle strengtening, instead of motor contol effect.
Intervention will be delivered by Physiotherapist with active right to physiotherapy practice.
The research will be held at "Pod Tezniami" Health Resort and Physiotherapy center in Ciechocinek, Poland.
All patients will receive the patient's informed consent form to participate in the research, they will be informed in detail about the course of the research and that they can resign from participation at any time.
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Control group
Active
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Outcomes
Primary outcome [1]
329293
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Foot Posture Index in Standing
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Assessment method [1]
329293
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Timepoint [1]
329293
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After 5-days training
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Primary outcome [2]
329294
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Distribution of feet loading during sitting/ standing up - non-invasive, on baroresistive / stabilometric platform
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Assessment method [2]
329294
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Timepoint [2]
329294
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After 5-days training
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Primary outcome [3]
329296
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Axis of lower legs during sitting/ standing up - non invasive 3-d motion analysis (Miomotion, Zebris or Ninox optical camera)
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Assessment method [3]
329296
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Timepoint [3]
329296
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After 5-days training
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Secondary outcome [1]
402040
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Movement of center of pressure in standing - Non invasive - stabilometric or baroresistive platform
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Assessment method [1]
402040
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Timepoint [1]
402040
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After 5-days training
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Secondary outcome [2]
402041
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Height of longitudinal arch during exercise - non invasive - picture with scale (mm) visible
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Assessment method [2]
402041
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Timepoint [2]
402041
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During excercise
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Secondary outcome [3]
402042
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Electric Activity of chosen lower limbs muscles during excercise (fEMG) -vastus lateralis and medialis muscles, tibialis anterior and peroneus longus - non-invasive, with surface EMG device
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Assessment method [3]
402042
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Timepoint [3]
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During excercise
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Secondary outcome [4]
402043
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Axis of lower limb during performance of excercise- non invasive 3-d motion analysis (Miomotion, Zebris or Ninox optical camera)
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Assessment method [4]
402043
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Timepoint [4]
402043
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During excercise
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Secondary outcome [5]
402044
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Maximal Isometric force of hip flexors and extensors - Non invasive, hand electrical dynamometer
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Assessment method [5]
402044
0
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Timepoint [5]
402044
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After 5-days training
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Secondary outcome [6]
402045
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range of passive and active movement in the first metatarsophalangeal joint - Non Invasive, goniomety
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Assessment method [6]
402045
0
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Timepoint [6]
402045
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After 5-days training
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Secondary outcome [7]
402046
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Ground reaction forces during gait on baroresistive platform (non-invasive)
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Assessment method [7]
402046
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Timepoint [7]
402046
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After 5-days training
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Secondary outcome [8]
404192
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Maximal Isometric force of hip abductors - Non invasive, hand electrical dynamometer
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Assessment method [8]
404192
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Timepoint [8]
404192
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After 5-days training
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Secondary outcome [9]
404193
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Maximal Isometric force of hip external rotators - Non invasive, hand electrical dynamometer
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Assessment method [9]
404193
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Timepoint [9]
404193
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After 5-days training
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Secondary outcome [10]
405625
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Maximal Isometric force of knee flexors and extensors - Non invasive, hand electrical dynamometer
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Assessment method [10]
405625
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Timepoint [10]
405625
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After 5-days training
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Eligibility
Key inclusion criteria
Occurrence of disturbances in the position of the lower limbs during resistance Closed Kinematic chain exercises - deviation of the knees inwards with equal load on the outer and inner parts of the feet, or loading of external part of the foot while maintaining axis of a lower legs
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Minimum age
20
Years
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Maximum age
70
Years
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Sex
Both males and females
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
• Inability to achieve the correctlower limb position during the exercise.
• Presence of significant pain in the lower limbs or the spine during the examination/ treatment
• Presence of congenital or traumatic defects related to deformations of the lower limbs, including the feet.
• Presence of weakness in the muscles of the lower extremities associated with impaired innervation or muscle atrophy.
• Occurrence of joint or muscle contractures of a structural nature, preventing the proper performance of the exercises.
• Previous lower limb correction surgery, partial or total lower limb arthroplasty
• Previous lumbar spine surgeries
• Contraindications to physical exercise in general, resistance exercises of the lower limbs in particular, including those related to the cardiovascular and nervous systems
• Degenerative changes in the joints of the lower extremities, grade III or IV, coexisting with pain
• Neurological disorders and diseases negatively affecting the control of lower limbs functions
• Lack of or limited contact with physiotherapist conducting the interventions, making it impossible to explain and / or understand the test conditions
• Using during the examination or within 2 days before it, targeted treatments correcting the settings of the pelvis and lower limbs, in particular manual therapy, osteopathic procedures, exercises according to neurophysiological methods or individual exercises with a therapist.
• Significant visual impairment and / or hearing loss making it difficult to use the Biofeedback phenomenon during exercise
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Allocation is not concealed
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Simple randomisation using procedures like coin-tossing and dice-rolling
Six walls dice will be used.
Paired number will be for research group
Non-paired for control group
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people receiving the treatment/s
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Intervention assignment
Parallel
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
According to literature and our possibilities, number of participants was specified as 80 to 120 persons, divided for both groups
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
7/02/2022
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Actual
16/02/2022
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Date of last participant enrolment
Anticipated
3/06/2022
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Actual
7/04/2022
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Date of last data collection
Anticipated
25/06/2022
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Actual
20/04/2022
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Sample size
Target
120
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Accrual to date
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Final
109
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Recruitment outside Australia
Country [1]
24235
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Poland
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State/province [1]
24235
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Kujawsko-pomorskie voivodenship
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Funding & Sponsors
Funding source category [1]
309958
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Commercial sector/Industry
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Name [1]
309958
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PHU Technomex, sp. z o. o.
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Address [1]
309958
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Szparagowa 15
44-141 Gliwice
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Country [1]
309958
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Poland
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Primary sponsor type
Individual
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Name
Michal Dylewski
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Address
Klinika Uzdrowiskowa "Pod Tezniami" im. Jana Pawla II, SUM
Michal Dylewski
Warzelniana 7
87-720 Ciechocinek
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Country
Poland
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Secondary sponsor category [1]
311003
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None
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Name [1]
311003
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Address [1]
311003
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Country [1]
311003
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
309673
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University of Mikolaj Kopernik in Torun, Colegium Medicum Bioethical Comitee
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Ethics committee address [1]
309673
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Ul. Marii Curie-Sklodowskiej 9 85-094 Bydgoszcz
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Ethics committee country [1]
309673
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Poland
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Date submitted for ethics approval [1]
309673
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04/01/2018
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Approval date [1]
309673
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16/01/2018
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Ethics approval number [1]
309673
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KB 59/2018
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Summary
Brief summary
Bioethical comitee aproval was extended to the june of 2022 in attachment. This approval is for wider range research, inckluding except described trial also assessment of effectiveness of Dynamic Taping for lower part of Spiral Line according to Myers. Both interventions (excercises described in this registartion) and dynamic taping share the same inclusion/ exclusion criteria, recruitment method and outcomes. Research are taken to confirm/ proof effects observed subjectively in clinical work on individual basis with dysfunctional patients.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Mr Michal Dylewski
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Address
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Klinika Uzdrowiskowa "Pod Tezniami" im. Jana Pawla II, SUM
Michal Dylewski
Warzelniana 7
87-720 Ciechocinek
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Country
114990
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Poland
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Phone
114990
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+48 609968793
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Fax
114990
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Email
114990
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[email protected]
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Contact person for public queries
Name
114991
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Michal Dylewski
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Address
114991
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Klinika Uzdrowiskowa "Pod Tezniami" im. Jana Pawla II, SUM
Michal Dylewski
Warzelniana 7
87-720 Ciechocinek
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Country
114991
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Poland
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Phone
114991
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+48 609968793
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Fax
114991
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Email
114991
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[email protected]
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Contact person for scientific queries
Name
114992
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Michal Dylewski
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Address
114992
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Klinika Uzdrowiskowa "Pod Tezniami" im. Jana Pawla II, SUM
Michal Dylewski
Warzelniana 7
87-720 Ciechocinek
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Country
114992
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Poland
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Phone
114992
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+48 609968793
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Fax
114992
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Email
114992
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
Due to European Commission regulations regarding personal data.
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What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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