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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT03284606
Other study ID # RC31/15/7839
Secondary ID 2016-A01552-49
Status Terminated
Phase N/A
First received
Last updated
Start date September 1, 2017
Est. completion date December 31, 2021

Study information

Verified date June 2022
Source University Hospital, Toulouse
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A majority of people undergoing rehabilitation following a stroke have a deficit of the dorsal flexors of the foot. The implementation of rehabilitation techniques in accordance with the recommendations of learned societies is not sufficient to compensate for this deficit. Also Kinesio Taping's method of Dr. Kenzo Kase has caught our attention by its action on muscle, joint, circulatory and pain functions. The use of taping would increase the duration of stimulation of the muscles of the dorsiflexors of the foot which would facilitate the motor recovery. Data from the literature do not support the conclusion that taping is effective, but no studies evaluating the efficacy of this technique in the foot-lift deficiency of the hemiplegic patient have been found. The investigators hypothesize that the use of taping in conjunction with common rehabilitation for hemiplegic patients following a stroke improves the stimulation of the muscles of the dorsiflexors of the foot with a positive impact on the walking.


Recruitment information / eligibility

Status Terminated
Enrollment 7
Est. completion date December 31, 2021
Est. primary completion date December 31, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patient with a stroke occurring in a period ranging from 15 days to a month before inclusion and presenting left or right hemiplegia. - Voluntary motricity of the dorsal flexors of the foot greater than or equal to 1 on the scale of Held and Pierrot Deseilligny - Quadriceps voluntary motor skill greater than or equal to 2 on the scale of Held and Pierrot Deseilligny - Informed consent of the patient. Exclusion Criteria: - - Evolutive neurological disease leading to cognitive impairment (Alzheimer's, Parkinson's, Multiple sclerosis ...) - Pre-stroke neurological sequelae - Achilles tendon elongation or tendinous transfer surgery. - Spasticity of the sural triceps greater than 2 on the modified Ashworth scale - Injection of botulinum toxin - Patients under guardianship, curatorships or under safeguard of justice. - Allergy to glue, skin lesions located on the zone of laying of the bands - Complex Regional Pain Symptom of the Ankle

Study Design


Related Conditions & MeSH terms


Intervention

Device:
TAPING
Taping in conjunction with common rehabilitation for hemiplegic patients
Procedure:
Common rehabilitation
Common rehabilitation for hemiplegic patients

Locations

Country Name City State
France University Hospital Toulouse Toulouse

Sponsors (2)

Lead Sponsor Collaborator
University Hospital, Toulouse Groupement Interrégional de Recherche Clinique et d'Innovation

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary voluntary muscularity voluntary muscularity measured by the quotation of Held and Pierrot Deseilligny Week 10
Secondary Spasticity score Ashworth scale modified for spasticity Week 10
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