Evaluation of the Concordance of Five Times Sit To Stand Results Between a Physical Consultation and a Teleconsultation
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In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Physical consultation, Teleconsultation.
- Who it may be relevant to
- Registry conditions: Rehabilitation, Elderly Person, Teleconsultation. Basic parameters: 65 years — 110 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- France
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Evaluation of the Concordance of Five Times Sit To Stand Results Between a Physical Consultation and a Teleconsultation of the Elderly
Overview
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.
Detailed description
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.
Tests are realized at baseline after randomization. The test with best time will be considered for analysis.
Once the 2 tests have been carried out, a satisfaction survey will evaluate the preference between the two tests for each patient.
Patients will be re-contacted by telephone at 3, 6 and 12 months post-inclusion to collect the number of falls.
Interventions
- Other 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. - Other 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 i
Primary outcome measures
- Five Time Sit To Stand test completion time in teleconsultation [Time frame: At inclusion]
- Five Time Sit To Stand test completion time in face-to-face consultation [Time frame: At inclusion]
Secondary outcome measures (5)
- Satisfaction questionnaire [Time frame: At inclusion]
- Five Time Sit To Stand test completion time in teleconsultation [Time frame: At inclusion]
- Five Time Sit To Stand test completion time in face-to-face consultation [Time frame: At inclusion]
- Presence or absence of falls [Time frame: At Month 3, Month 6 and Month 12]
- Number of falls [Time frame: At Month 3, Month 6 and Month 12]
Eligibility criteria
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.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Crossover
- Masking
- Open label
- Primary purpose
- Other
Study locations
France · 2 centers
- ILDYS Ty Yann — Brest
- Institut de réadaptation du Cap Horn — Landerneau
Identifiers
NCT: NCT06365177 · 29BRC22.0243