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Study Human Digital Support Transitional Care (SUNH-ST)

D

Divoluci

Status

Not yet enrolling

Conditions

Aging

Treatments

Procedure: Unscheduled hospital admissions

Study type

Interventional

Funder types

Other

Identifiers

NCT06354166
2023-A02745-40

Details and patient eligibility

About

The purpose of the study is to compare the effectiveness of Divomed in organising complex hospital discharges with a conventional organisation. Effectiveness will be assessed by reducing the length of stay of patients in geriatric short-stay care.

Full description

This is an interventional, randomised (ratio 1:1), single-centre, open-label study evaluating Divomed, a digital tool combined with human coordination, to speed up the discharge of people aged over 75 from unscheduled short-stay geriatric hospital admissions to their homes.

The study population will be patients aged 75 or over, admitted for short term unscheduled geriatric hospitalisation and eligible for discharge home.

Enrollment

150 estimated patients

Sex

All

Ages

75+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age ≥ 75 years ;
  • Unplanned hospitalisation from emergency, transfers from other inpatient departments or outpatient medicine;
  • Patient eligible for short-stay geriatric hospitalisation estimated to last at least 10 days;
  • Patient eligible for a return home;
  • Patients who have been informed and have signed an informed consent form. If necessary (for cognitive or other reasons), the information must be given to a third party, i.e. the patient's legal representative or trusted person (independent of the investigator and the sponsor), who may be asked to sign or co-sign the informed consent form (depending on the patient's vulnerability).

Exclusion criteria

  • Patients scheduled for transfusion, iron infusion or colonoscopy;
  • Patients in palliative care;
  • Geographical area other than department 37;
  • Planned discharge from hospital to a residential establishment for dependent elderly people or to follow-up and rehabilitation care or long-term care units;
  • Patient or deprived of liberty by judicial or administrative decision ;
  • Patient participating in or being excluded from another clinical trial;
  • Patients not covered by a social security scheme.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

150 participants in 2 patient groups

Divomed digital tool combined with human coordination
Experimental group
Description:
A digital tool combined with human coordination (Divomed) to organise discharge home from the start of hospitalisation. The digital application will be interconnected with the patient's medical file.
Treatment:
Procedure: Unscheduled hospital admissions
Control Group
Active Comparator group
Description:
The control group corresponds to the organisation of conventional hospital discharge from the geriatric short-stay department. The digital application will be interconnected with the patient's medical file.
Treatment:
Procedure: Unscheduled hospital admissions

Trial contacts and locations

1

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Central trial contact

Wassim GANA

Data sourced from clinicaltrials.gov

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