Cognitive DeteriorationSafEENCT02288221
Safe & Easy Environment at Home for Patients Presenting a Frail Syndrome
A study testing Patient's answer with non pharmacological therapeutic and Patient's answer without non pharmacological therapeutic in people with Cognitive Deterioration, run by Centre Hospitalier Universitaire de Nice at 1 site in France.
Trial summary
All over the world the increasing prevalence of chronic disorders and its impact on functional decline is challenging the sustainability of health care systems. Older individuals also frequently experience the reversible "frailty syndrome", which overlaps with chronic diseases, increasing incidence of disability. Read more about this study
- Who is it for?
- Ages 60 years and older
- Conditions the study is for
- Cognitive Deterioration
- What is being tested?
- Patient's answer with non pharmacological therapeutic and Patient's answer without non pharmacological therapeutic
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 4 participants
- Where
- 1 siteFrance
- Study dates
- 4 Jun 2015to 5 Jul 2017
- Phase
- Interventional
- Are there results?
- None posted in the registry
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 60 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Male or female age ≥ 60 years with memory complaint
- Score at the Mini Mental Test (MMSE) ≥ 26.
- Score at the Clinical Dementia Rating Scale (CDR) ≤ 0.5.
Who cannot join
- Sensory defect (visual or olfactory) preventing the patient to perfectly meet therapeutic solutions.
- Prescription new psychotropic medication (hypnotic, anxiolytic, antidepressant, antipsychotic) in the week preceding the assessment.
- Subject epileptic.
- Subject vulnerable
Trial locations and contacts
1 site in 1 country.
About this study
Official title: SafEE : Safe & Easy Environment at Home for Patients Presenting a Frail Syndrome
All over the world the increasing prevalence of chronic disorders and its impact on functional decline is challenging the sustainability of health care systems. Older individuals also frequently experience the reversible "frailty syndrome", which overlaps with chronic diseases, increasing incidence of disability.
Building a global system aiming to take in charge all causes leading to loss of autonomy is a rather complicated task involving numerous Information and Communication technologies (ICT) solutions which are not always easy to use in everyday life.
Read more
The SafEE (Safe Easy Environment) project aim is to improve the safety, autonomy and quality of life of older people at risk.
The SafEE project develop non pharmacological therapeutic through diferent ICT (stimulation aromatherapy automatic fragrance, training interface based on Kinect sensor...) .
The goal of this study is to validate the acceptability, sensitivity and efficacy of the systems.
Read the detailed description
The non pharmacological therapeutic will be install at patient's home :
- aromatherapy,
- music therapy,
- cognitive training in multimedia application offering cognitive games.
Also smart phone will be given to the patient :
- to help him move with a geolocation application,
- to remind him of his daily needs (shopping lists, people to call, etc ...) with an alert apllication.
- Conditions
- Cognitive Deterioration
- Being tested
- Patient's answer with non pharmacological therapeutic, Patient's answer without non pharmacological therapeutic
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Patient's answer with non pharmacological therapeuticOther
Installation at patient's home of :
- aromatherapy
- music therapy
- cognitive training in multimedia application offering cognitive games
Patient's answer without non pharmacological therapeuticOther
No installation at patient's home
| Study group | Role | What they receive |
|---|---|---|
| With non pharmacological therapeutic | Experimental | Installation of ICT at patient's home Receives: Other: Patient's answer with non pharmacological therapeutic |
| Without non pharmacological therapeutic | Active comparator | No change at patient's home Receives: Other: Patient's answer without non pharmacological therapeutic |
What is being measured
The primary outcome is the main question the study is designed to answer.
Time spent by the patient using the non-therapeutic solutions
Measured: 6 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted11 Nov 2014 (estimated)
- Study start4 Jun 2015
- Primary completion5 Jul 2017
- Study completion5 Jul 2017
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Cognitive DeteriorationStudies of the same condition, open and under way.
- More trials run by Centre Hospitalier Universitaire de NiceThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 4 participants (actual)
Sponsor and investigators
- Lead sponsor
- Centre Hospitalier Universitaire de Nice
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Renaud DAVID, Dr, Study director, Centre Hospitalier Universitaire de Nice
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02288221
- Sponsor's protocol ID
- 14-PP-04
- Acronym
- SafEE
- Status last verified
- Nov 2025
- First submitted
- 19 Aug 2014
- Last updated
- 2 Dec 2025
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 2 Dec 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- SafEE : Safe & Easy Environment at Home for Patients Presenting a Frail Syndrome
- ClinicalTrials.gov ID
- NCT02288221
- Acronym / sponsor ID
- SafEE / 14-PP-04
- Conditions
- Cognitive Deterioration
- Study type
- Interventional
- Recruitment status
- Terminated
- Enrolment
- 4 participants (actual)
- Lead sponsor
- Centre Hospitalier Universitaire de NiceUniversity, hospital or other
- Study start
- 4 Jun 2015 (actual)
- Primary completion
- 5 Jul 2017 (actual)
- Study completion
- 5 Jul 2017 (actual)
- First posted
- 11 Nov 2014 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
All over the world the increasing prevalence of chronic disorders and its impact on functional decline is challenging the sustainability of health care systems. Older individuals also frequently experience the reversible "frailty syndrome", which overlaps with chronic diseases, increasing incidence of disability.
Building a global system aiming to take in charge all causes leading to loss of autonomy is a rather complicated task involving numerous Information and Communication technologies (ICT) solutions which are not always easy to use in everyday life.
The SafEE (Safe Easy Environment) project aim is to improve the safety, autonomy and quality of life of older people at risk.
The SafEE project develop non pharmacological therapeutic through diferent ICT (stimulation aromatherapy automatic fragrance, training interface based on Kinect sensor...) .
The goal of this study is to validate the acceptability, sensitivity and efficacy of the systems.
Detailed description
The non pharmacological therapeutic will be install at patient's home :
- aromatherapy,
- music therapy,
- cognitive training in multimedia application offering cognitive games.
Also smart phone will be given to the patient :
- to help him move with a geolocation application,
- to remind him of his daily needs (shopping lists, people to call, etc ...) with an alert apllication.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| With non pharmacological therapeutic | Experimental | Other: Patient's answer with non pharmacological therapeuticInstallation of ICT at patient's home |
| Without non pharmacological therapeutic | Active comparator | Other: Patient's answer without non pharmacological therapeuticNo change at patient's home |
Who may qualify
- Ages
- 60 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- Male or female age ≥ 60 years with memory complaint
- Score at the Mini Mental Test (MMSE) ≥ 26.
- Score at the Clinical Dementia Rating Scale (CDR) ≤ 0.5.
Key exclusion criteria (4 listed)
- Sensory defect (visual or olfactory) preventing the patient to perfectly meet therapeutic solutions.
- Prescription new psychotropic medication (hypnotic, anxiolytic, antidepressant, antipsychotic) in the week preceding the assessment.
- Subject epileptic.
- Subject vulnerable
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Patient's answer with non pharmacological therapeuticInstallation at patient's home of : * aromatherapy * music therapy * cognitive training in multimedia application offering cognitive games | Other | With non pharmacological therapeutic |
| Patient's answer without non pharmacological therapeuticNo installation at patient's home | Other | Without non pharmacological therapeutic |
Primary outcome
Time spent by the patient using the non-therapeutic solutions
Time frame: 6 months
Results and safety
The study was stopped early. Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 2 Dec 2025.
Related trials for Cognitive Deterioration
Not yet recruitingObservational study
Cognitive Outcomes in BAD-related Stroke
Branch Atheromatous Disease, Cognitive
Active, not recruiting
Exercise Effects on Health Status in Patients With Severe Mental Illness
Exercise, Metabolic Syndrome
RecruitingObservational study
Alzheimer's Disease Treatment With Combination of 40Hz Light and Cognitive Therapy
Alzheimer Disease, Mild Cognitive Impairment
RecruitingObservational study
Virtual perI-/Menopause Registry of AusTrALia
Menopause, Perimenopausal Disorder
Not yet recruitingObservational study
Effects of Petroleum Compounds on Psychological Health and Cognitive Functions
Cognitive Deterioration
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Renaud DAVID, Dr study director
Centre Hospitalier Universitaire de Nice
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Patient's answer with non pharmacological therapeutic and Patient's answer without non pharmacological therapeutic in people with Cognitive Deterioration, run by Centre Hospitalier Universitaire de Nice 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 3 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: stopped early, as of the sponsor's last update on 2 Dec 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?
The study was stopped early. Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Time spent by the patient using the non-therapeutic solutions (time frame: 6 months). 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 2 Dec 2025.