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GeriatricUMG-CHUSENCT07073001

Three-month Follow-up Analysis of Social Recommendations Issued by the Mobile Geriatric Team

An observational study of Geriatric and Care Coordination, run by Centre Hospitalier Universitaire de Saint Etienne at 1 site in France.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

This single-center, prospective, observational cohort study aims to evaluate the actual implementation rate of social recommendations formulated by the Mobile Geriatric Team at Saint-Étienne University Hospital three months after hospital discharge. Read more about this study

Who is it for?
Ages 75 years and older
What is being tested?
Telephone interview
How many people
100 participants
Where
1 siteFrance
Study dates
Sep 2025to Jan 2026
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 75 years and older
  • All sexes
  • No healthy volunteers
  • Older adult

Study population: Any patient who has benefited from an assessment by the CHUSE EMG with formulation of social recommendations between August 1, 2025 and January 31, 2026 will be included.

Who may be able to join

  • Patients aged 75 years or older
  • Patients assessed by the Mobile Geriatric Team of the Saint-Etienne University Hospital with the formulation of social recommendations
  • Patients residing at home or in a long-term care facility for dependent elderly individuals (nursing home / EHPAD)
  • Informed consent obtained from the patient or their legal representative

Who cannot join

  • Patients under 75 years old
  • Refusal to participate in the study by the patient (or by the legally authorized representative/trusted person).
  • Patients receiving exclusive palliative care
  • Inability to ensure follow-up: in case of non-response at three months or in the event of death

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

France1 site
  • CHU Saint-Etienne

    Saint-Etienne, 42100

Other trials in France

About this study

Official title: UMG-CHUSE Study: Three-month Follow-up Analysis of Social Recommendations Issued by the Mobile Geriatric Team.

This single-center, prospective, observational cohort study aims to evaluate the actual implementation rate of social recommendations formulated by the Mobile Geriatric Team at Saint-Étienne University Hospital three months after hospital discharge. These recommendations may include human assistance, technical aids, financial aid applications, legal protective measures, or referrals to appropriate care structures.

A structured telephone interview at three months will assess the degree of implementation, explore associated barriers (administrative, cognitive, organizational, ...), and investigate any potential link with hospital readmissions or changes in patients' living situations.

Being tested
Telephone interview
Keywords
Geriatrics, Mobile Geriatric Team, Care coordination, Social recommandations, Elderly care, Hospital readmission

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Telephone interviewOther

    A structured telephone interview at three months will assess the degree of implementation, explore associated barriers (administrative, cognitive, organizational, ...), and investigate any potential link with hospital readmissions or changes in patients' living situations.

Study groups in NCT07073001
Study groupRoleWhat they receive
Patients includedPatients aged 75 and over who have been assessed by the CHUSE mobile geriatrics team and have received social recommendations.
Receives: Other: Telephone interview

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Rate of implementation of social recommendations

    Evaluate the three-month implementation rate of the total social recommendations issued by the mobile geriatric team.

    Measured: Month : 3

Secondary outcomes (4)
  1. Factors hindering the implementation of recommendations

    Identify the factors holding back the implementation of TOTAL recommendations (then SPECIFIC: human, technical, financial, patient orientation, implementation of legal protection measures).

    Measured: Month : 3

  2. Reasons for refusal or non-implementation

    Analyze the reasons for refusal or non-implementation.

    Measured: Month : 3

  3. Impact of non-implementation on the re-hospitalization rate

    Evaluate the impact of non-implementation on the re-hospitalization rate.

    Measured: Month : 3

  4. Patient's living environment

    Document changes in the patient's living environment at three months.

    Measured: Month : 3

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted18 Jul 2025
  2. Study startSep 2025 (estimated)
  3. Primary completionJan 2026 (estimated)
  4. Study completionJan 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
100 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07073001
Sponsor's protocol ID
IRBN692025/CHUSTE
Acronym
UMG-CHUSE
Status last verified
Aug 2025
First submitted
9 Jul 2025
Last updated
11 Aug 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Geriatric and Care Coordination, run by Centre Hospitalier Universitaire de Saint Etienne at 1 site in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 11 Aug 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Manon SAHUC ((0)477127034 ext. +33, manon.sahuc2@etu.univ-st-etienne.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Rate of implementation of social recommendations (time frame: Month : 3). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Aug 2025.

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