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Starting soon Not applicable

A Clinical Decision Support Tool for Assessing the Ability to Decide on Returning Home in Elderly Patients with Cognitive Impairments

NCT06669559 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2025-01
Last updated
2024-11-01

Condition(s) studied

The Patient's Ability to Decide to Return Home After Hospitalization

Investigational drug(s) / intervention(s)

DROM-Test

DROM-Test: DROM test: a tool for assessing the ability to decide on returning home

Study summary

No validated and generalized tool for assessing a patient's ability to decide whether to return home after hospitalization exists. Evaluating the capacity of elderly patients to decide on their own return home is a daily concern for geriatricians. Neurocognitive disorders do not necessarily mean an inability to decide and the MMSE (mini mental state examination), a reference scale for screening neurocognitive disorders, is not sufficient to determine decision-making capacity apart from extreme scores. Depending on the stage or type of neurocognitive disorders, the same stages of the decision-making process (understanding, reasoning, appreciation, choice) are not impacted. The ability to decide depends on the type of decision (deciding to vote, deciding to take a medication, to participate in clinical research, etc.), i.e. domain-dependent. Associating the clinician's clinical decision with a standardized tool for assessing patients' capacity to decide would enable more ethical clinical practice.

the aim of the study is to add to the clinical decision a decision support tool to assess the capacity to decide whether to return home has better sensitivity in the assessment of the capacity to decide than that of clinical assessment alone

Eligibility

Sex
ALL
Min age
70 Years
Max age
—
Healthy volunteers
No
Inclusion criteria: * 70 years and over * neurocognitive disorders regardless of diagnosis * MMSE between 15 and 25 * hospitalized in geriatrics * still living at home at the time of hospitalization * affiliated to or beneficiary of a social security scheme Non-inclusion criteria * confusional episode, * palliative care, * presence of another significant or systemic pathology: Cerebral Vascular Accident \< 3 months, oncological pathology during treatment, decompensated psychiatric illness, acute organ failure, * total visual or hearing deficit, * has already taken the DROM test during a previous hospitalization, * language barrier, * refusal of participation by the patient, their relative or guardian if applicable * patient under judicial protection

Primary outcome measure(s)

  • Sensitivity of the DROM test — 3 days
    Ability of the DROM test to accurately identify true positives, meaning patients who truly have the capacity to decide on returning home, according to the gold standard

Trial sites (1)

FacilityCityRegionStatus
Hôpital Bretonneau Paris France
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06669559 on ClinicalTrials.gov ↗ ← All trials in France