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Recruiting Not applicable

Evaluation of the Concordance of Five Times Sit To Stand Results Between a Physical Consultation and a Teleconsultation

NCT06365177 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2024-06-20
Last updated
2024-07-05

Condition(s) studied

RehabilitationElderly PersonTeleconsultation

Investigational drug(s) / intervention(s)

Physical consultationTeleconsultation

Physical consultation: The subject enters a room where the therapist is present. A chair is placed against a wall in the same room. Once again, the therapist suggests repeating the test. During the test, the therapist sits opposite the patient, at the same distance as the computer used during the teleconsultation.

Teleconsultation: Prior to the test, the investigator should carry out a "mock" test with a volunteer from the facility, for example, to ensure wifi, sound and image functionality. The patient enters a room where a computer equipped with a webcam is set up on a desk. The teleconsultation has already started when the patient enters the room. No recordings are made. A chair is placed at a distance from the desk, with the backrest against a wall. The chair faces the computer. The desk or table where the computer is located is about 3 meters from the participant, ensuring that the webcam can frame the patient's entire body during the test. With the consultation already underway, the investigator can direct the patient to sit in the chair against the wall. The investigator will make sure that the patient hears the instructions given. Once the patient is seated on the chair, the therapist explains the test procedure and shows it once to make sure the subject understands it.

Study summary

This study concerns elderly person aged more than 65 years with autonomous mobility.

It is a multicentric randomized trial in two arms :

Arm one : remote consultation then physical consultation Arm two : physical consultation then remote consultation

Consultations consist to take a Five Times Sit To Stand test, in physical consultation with physiotherapist in the same room and in remote consultation with a physiotherapist in the next room to the patient.

Eligibility

Sex
ALL
Min age
65 Years
Max age
110 Years
Healthy volunteers
No
Inclusion Criteria: * Volunteers over the age of 65. * Elderly people who can walk and move around independently. * Subjects capable of giving informed consent. * GIR 3,4,5,6. * Affiliated to a Social Security scheme. Exclusion Criteria: * GIR \< 3 * Major visual and/or hearing impairment (known pathology and not fitted with hearing aids) * Patient deprived of liberty by judicial or administrative decision, under guardianship or curatorship * Subject having refused to participate. * Subject at risk of syncope on rising (cardiac pathologies, orthostatic hypotension). * Subjects with known vestibular disorders.

Primary outcome measure(s)

  • Five Time Sit To Stand test completion time in teleconsultation — At inclusion
    The physiotherapist is present in a room at a distance from the patient's consultation room. The Five Time Sit to Stand (FTSS) is a functional assessment that requires a chair and a stopwatch. The patient is timed from start to finish. The time taken to complete the test is expressed in minutes. The patient performs two trials. The best result is retained for analysis.
  • Five Time Sit To Stand test completion time in face-to-face consultation — At inclusion
    The physiotherapist is present in the same consulting room as the patient. The Five Time Sit to Stand (FTSS) is a functional assessment that requires a chair and a stopwatch. The patient is timed from start to finish. The time taken to complete the test is expressed in minutes. The patient performs two trials. The best result is retained for analysis.

Trial sites (2)

FacilityCityRegionStatus
ILDYS Ty Yann Brest France Recruiting
Institut de réadaptation du Cap Horn Landerneau France Active Not Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06365177 on ClinicalTrials.gov ↗ ← All trials in France