Actively Recruiting

Phase Not Applicable
Age: 50Years +
All Genders
ID07492745

Effect of Using a Reminder to Encourage Patients to be Active During Their Hospital Stay: a Multicenter Randomised Controlled Double Blind Study

Led by Groupe Hospitalier du Havre · Updated on 2026-04-22

204

Participants Needed

4

Research Sites

13 weeks

Total Duration

On this page

Sponsors

G

Groupe Hospitalier du Havre

Lead Sponsor

C

Centre Hospitalier de Valence

Collaborating Sponsor

AI-Summary

What this Trial Is About

About 30% of patients aged 65 and older experience a decline in their ability to function after being hospitalized. This decline often results from spending too much time inactive during hospital stays, which can lead to loss of independence and muscle strength. The study aims to evaluate whether using a vibrating watch as a reminder to encourage physical activity can help improve patients' functional capacity during their hospital stay. Participants will receive usual care from physiotherapists, including walking, muscle strengthening exercises, and respiratory physiotherapy if needed. They will be randomly assigned to one of two groups: one group will receive a vibrating watch set to vibrate six times a day as a prompt to exercise or walk, while the control group will receive a watch that vibrates once daily. Patients will be asked to perform the prescribed exercises independently each time the watch vibrates. During the study, researchers will assess physical activity levels, functional independence, compliance with exercises, and quality of life at various time points, including within 24 hours of admission and 48 hours before discharge, as well as three months after discharge. They will also monitor falls and rehabilitation volume and location. Participants' progress will be closely followed to understand the impact of these reminders on their recovery and safety over time.

CONDITIONS

Brief Title

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

Who Can Participate

Age: 50Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 50 or older with a Clinical Frailty Scale score of 4 or above (vulnerable but not dependent).
  • Ability to get up from a chair without assistance.
  • Ability to communicate with staff, understand instructions, give consent, and cooperate with staff.
Not Eligible

You will not qualify if you...

  • Estimated hospital stay less than 5 days.
  • Contraindications to physical activity determined by the medical team (e.g., cardiovascular instability, orthopedic issues).
  • Terminal illness.
  • Scheduled for surgery.
  • Pregnant women.
  • Individuals who do not understand French.
  • People protected under the law.

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - Duration of hospital stay, at least 5 days

Participants will receive a vibrating reminder device set to prompt them to perform prescribed muscle strengthening exercises or walking multiple times per day during their hospital stay. Exercises will be tailored to their physical abilities and environmental constraints.

Routine hospital visits during stay

Follow-up

Duration - 3 months after discharge

Participants will be monitored for functional capacity, physical activity, rehabilitation, quality of life, and falls up to 3 months after hospital discharge.

1 visit at 3 months after discharge

Trial Site Locations

Total: 4 locations

1

Hôpital Erasme Route de Lennick 808

Brussels, Belgium, 1070

Not Yet Recruiting

2

Groupe Hospitalier du Havre

Le Havre, Normandy, France, 76290

Actively Recruiting

3

Centre hospitalier de Chartres

Le Coudray, France, 28630

Not Yet Recruiting

4

centre hospitalier de Valence

Valence, France, 26000

Not Yet Recruiting

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Research Team

G

Guillaume Prieur, PT, PhD

Y

Yann Combret, PT, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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