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Videographic Feedback and Walk Rehabilitation in Post-Cerebrovascular Accident

NCT ID: NCT05024981

Last Updated: 2024-12-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

64 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-03-04

Study Completion Date

2027-01-04

Brief Summary

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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.

Detailed Description

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Conditions

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Cerebrovascular Accident

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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Classic reeducation

Group Type ACTIVE_COMPARATOR

Classic reeducation

Intervention Type BEHAVIORAL

The patient will benefit twice a day for 30 minutes from re-education sessions.

Classic reeducation + videographic feedback

Group Type EXPERIMENTAL

Videographic feedback

Intervention Type BEHAVIORAL

Twice a week during his classic re-education sessions, the patient will be filmed for 1 minute. After transferring the video to a tablet, he will watch the video once and decide what he wants to correct. During the second viewing, he will analyse his walk, the therapist being present to provide additional information. Finally, the patient will apply his analysis while being filmed and will compare the possible differences between the 2 videos. Depending on the time available, the patient may have to repeat the recordings, analyses and exercises.

Interventions

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Videographic feedback

Twice a week during his classic re-education sessions, the patient will be filmed for 1 minute. After transferring the video to a tablet, he will watch the video once and decide what he wants to correct. During the second viewing, he will analyse his walk, the therapist being present to provide additional information. Finally, the patient will apply his analysis while being filmed and will compare the possible differences between the 2 videos. Depending on the time available, the patient may have to repeat the recordings, analyses and exercises.

Intervention Type BEHAVIORAL

Classic reeducation

The patient will benefit twice a day for 30 minutes from re-education sessions.

Intervention Type BEHAVIORAL

Eligibility Criteria

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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.
Minimum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Centre Hospitalier Universitaire de Nice

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Audrey MARTEU

Role: PRINCIPAL_INVESTIGATOR

Centre Hospitalier Universitaire de Nice

Locations

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CHU Nice

Nice, Alpes-Maritime, France

Site Status RECRUITING

Countries

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France

Central Contacts

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Audrey MARTEU

Role: CONTACT

Phone: 4 92 03 40 80

Email: [email protected]

Facility Contacts

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Audrey MARTEU

Role: primary

Other Identifiers

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19-GIRCI-02

Identifier Type: -

Identifier Source: org_study_id