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Recruiting Not applicable NCT07492745

Effect of Using a Reminder to Encourage Patients to be Active During Their Hospital Stay.

No applicable phase (e.g. observational)
Conditions: Inpatients Frail

Sponsor: Groupe Hospitalier du Havre

trial.available_in: БГ
Overview
Around 30% of patients aged 65 and over experience functional decline due to hospitalization. Physical inactivity, often without medical justification, is common during hospital stays.This immobility leads to loss of autonomy, muscle strength, and increases post-discharge risks. Slow walking for 25-40 minutes daily significantly improves functional capacity. However, it could be difficult to reach this time of walking due to a lack of physiotherapist in hospital. A vibrating watch may encourage patients to walk or perform strengthening exercises. This simple intervention aims to improve function without requiring additional staff or resources
Description
30% of patients aged 65 or older will experience a decline in functional capacity as a result of hospitalization. Illness and hospitalization increase sedentary behavior in patients. It is common for patients to spend long periods of time resting in bed, regardless of their primary reason for admission. During hospitalization, nearly 60% of episodes of bed rest have no documented medical indications. Low physical activity during hospitalization can lead to impaired independence, loss of muscle strength, and decreased functional capacity. These losses in frail individuals are associated with increased disability and lead to a critical 30-day period after hospital discharge that exacerbates deconditioning. This period of increasing functional vulnerability can lead to readmission to hospital, disability, institutionalization, morbidity, and early mortality. The results of a meta-analysis show that walking slowly for about 25-40 minutes per day is sufficient to improve patients' functional capacity during hospitalization. The organization of care to promote patient mobility must be reviewed to make patients more involved in their care and more independent. It has been demonstrated for some time that the use of a reminder system (e.g., alarm) is a factor that promotes increased patient adherence to their treatments. The advantage of a vibrating reminder is that it is simple to use, very inexpensive, easy to implement in all hospital wards, and does not require additional human resources. The main hypothesis of this study is that the use of a vibrating watch set to 6 reminders per day to prompt patients to perform muscle strengthening exercises or walk a distance determined by the rehabilitation professional will increase patients' functional capacity.
Who can participate
Inclusion Criteria: * Patients aged 50 or over with a score of 4 or above on the Clinical Frailty Scale (vulnerable but not dependent patients, symptoms limiting activities, patients who are slower/more fatigued). * Must be able to get up from a chair without assistance. * Patients must be able to communicate with staff, understand instructions, give consent, and cooperate with staff. Exclusion Criteria: * Patients with an estimated hospital stay of less than 5 days. * Contraindications to physical activity determined by the medical team (e.g., cardiovascular instability, orthopedic contraindications, etc.). * Terminal illness. * Patients scheduled for surgery. * Pregnant women. * People who do not understand French. * People protected under the law.
Interventions
Vibrating reminder
DEVICE
Control group
DEVICE
Locations 4
Belgium (1)
Hôpital Erasme Route de Lennick 808
Brussels
NOT_YET_RECRUITING
France (3)
Centre hospitalier de Chartres
Le Coudray
NOT_YET_RECRUITING
Gaëtan BADRE, Infirmier recherche clinique
Groupe Hospitalier du Havre
Le Havre , Normandy
centre hospitalier de Valence
Valence
NOT_YET_RECRUITING
Baptiste Fontanille, MKDE
Technical details
Status
Recruiting
Phase
Not applicable
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
50 Years
Healthy volunteers
No
Start date
19.11.2025
Completion date
01.01.2029
Registry ID
NCT07492745
Source
clinicaltrials.gov
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