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NCT Number: NCT05024981

Videographic Feedback and Walk Rehabilitation in Post-Cerebrovascular Accident

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.

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Key information

Age range

70 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

CHU Nice

Nice, Alpes-Maritime, 06000, France

Location status: Recruiting

Location contact

Audrey MARTEU

CONTACT

[email protected]

4 92 03 40 80 ext. +33

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Videographic feedback

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.

Classic reeducation

Behavioral

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

Primary outcomes

  1. Walking speed

    Time frame: Day 26

    Difference in walking speed between the initial and final assessment in each group.

Study contacts

Contact information is provided by the study sponsor or research team.

Audrey MARTEU

CONTACT

[email protected]

4 92 03 40 80 ext. +33

Sponsors and collaborators

Lead sponsor

Centre Hospitalier Universitaire de Nice

Other

Registry information

Acronym: CoDévi

Important dates

Study start
2022
Primary completion
2027
Study completion
2027
First posted
Aug 27, 2021
Registry last updated
Dec 11, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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