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Videographic Feedback and Walk Rehabilitation in Post-Cerebrovascular Accident (CoDévi)

C

Centre Hospitalier Universitaire de Nice

Status

Enrolling

Conditions

Cerebrovascular Accident

Treatments

Behavioral: Videographic feedback
Behavioral: Classic reeducation

Study type

Interventional

Funder types

Other

Identifiers

NCT05024981
19-GIRCI-02

Details and patient eligibility

About

Cerebrovascular Accident affects the majority of the elderly population and its frequency is constantly increasing. The resulting deficits are numerous and lead in particular to an alteration in the quality of walking and autonomy. Numerous rehabilitation techniques have been described. In practice, correction instructions are often given by the therapist while the motor activity is being performed. Walking is a complex activity, as is the processing of dual-task information in elderly stroke patients. It therefore appears interesting to separate the time of motor realization and that of correction instructions. Investigators therefore propose firstly to film the patient during the performance of a walking activity and then, secondly, to analyse the video with the patient, which thus represents a source of delayed feedback. The main objective of the study is to observe the effects of this practice on walking speed. Investigators are comparing two groups of patients: the control group receiving conventional rehabilitation and the experimental group receiving conventional rehabilitation plus sessions with the video tool. They expect to observe a greater improvement in walking speed in the experimental group.

Enrollment

64 estimated patients

Sex

All

Ages

70+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Hospitalization for a first episode of Cerebrovascular Accident less than six months old, or nth stroke less than six months old, with no previous sequelae;
  • Able to walk at least 10m without stopping, with or without technical assistance, but without human assistance, under supervision;

Exclusion criteria

  • Palliative or life-threatening situation;
  • A patient whose guardian or trustee is not readily available to provide information about the patient
  • Neuro-cognitive disorder that prevents understanding of instructions, as determined by the clinician;
  • Severe speech or language disorder that prevents the protocol from being carried out correctly;
  • Hemineglect;
  • Any previously known pathology altering the gait pattern, at the clinician's discretion (recent neurological, traumatological or orthopaedic pathologies, etc.);
  • Visual disorder preventing viewing of the video;
  • Hearing disorder preventing comprehension.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

64 participants in 2 patient groups

Classic reeducation
Active Comparator group
Treatment:
Behavioral: Classic reeducation
Classic reeducation + videographic feedback
Experimental group
Treatment:
Behavioral: Videographic feedback

Trial contacts and locations

1

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Central trial contact

Audrey MARTEU

Data sourced from clinicaltrials.gov

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